abdominal 1 neuroblast MNB [FBbt_00052507]
Any neuroblast MNB (FBbt:00001419) that is part of some abdominal segment 1 (FBbt:00000022).
Any neuroblast MNB (FBbt:00001419) that is part of some abdominal segment 1 (FBbt:00000022).
Any neuroblast NB1-2 (FBbt:00001384) that is part of some abdominal segment 1 (FBbt:00000022).
Any neuroblast NB2-4 (FBbt:00001411) that is part of some abdominal segment 1 (FBbt:00000022).
Any neuroblast NB2-5 (FBbt:00001374) that is part of some abdominal segment 1 (FBbt:00000022).
Any neuroblast NB3-2 (FBbt:00001388) that is part of some abdominal segment 1 (FBbt:00000022).
Any neuroblast NB3-5 (FBbt:00001375) that is part of some abdominal segment 1 (FBbt:00000022).
Any neuroblast NB5-2 (FBbt:00001376) that is part of some abdominal segment 1 (FBbt:00000022).
Any neuroblast NB5-3 (FBbt:00001390) that is part of some abdominal segment 1 (FBbt:00000022).
Any neuroblast NB6-1 (FBbt:00001398) that is part of some abdominal segment 1 (FBbt:00000022).
Any neuroblast NB6-2 (FBbt:00001391) that is part of some abdominal segment 1 (FBbt:00000022).
Any neuroblast NB7-1 (FBbt:00001380) that is part of some abdominal segment 1 (FBbt:00000022).
Any neuroblast NB7-4 (FBbt:00001381) that is part of some abdominal segment 1 (FBbt:00000022).
Any neuroblast NB3-5 (FBbt:00001375) that is part of some abdominal segment 2 (FBbt:00000023).
Any neuroblast NB5-2 (FBbt:00001376) that is part of some abdominal segment 2 (FBbt:00000023).
Any neuroblast NB5-3 (FBbt:00001390) that is part of some abdominal segment 2 (FBbt:00000023).
Any neuroblast NB6-2 (FBbt:00001391) that is part of some abdominal segment 2 (FBbt:00000023).
Any neuroblast NB3-5 (FBbt:00001375) that is part of some abdominal segment 3 (FBbt:00000024).
Any neuroblast NB5-2 (FBbt:00001376) that is part of some abdominal segment 3 (FBbt:00000024).
Any neuroblast NB5-3 (FBbt:00001390) that is part of some abdominal segment 3 (FBbt:00000024).
Any neuroblast NB3-5 (FBbt:00001375) that is part of some abdominal segment 4 (FBbt:00000025).
Any neuroblast NB5-2 (FBbt:00001376) that is part of some abdominal segment 4 (FBbt:00000025).
Any neuroblast NB5-3 (FBbt:00001390) that is part of some abdominal segment 4 (FBbt:00000025).
Any neuroblast NB3-5 (FBbt:00001375) that is part of some abdominal segment 5 (FBbt:00000026).
Any neuroblast NB5-2 (FBbt:00001376) that is part of some abdominal segment 5 (FBbt:00000026).
Any neuroblast NB5-3 (FBbt:00001390) that is part of some abdominal segment 5 (FBbt:00000026).
Any neuroblast NB3-5 (FBbt:00001375) that is part of some abdominal segment 6 (FBbt:00000027).
Any neuroblast NB5-2 (FBbt:00001376) that is part of some abdominal segment 6 (FBbt:00000027).
Any neuroblast NB5-3 (FBbt:00001390) that is part of some abdominal segment 6 (FBbt:00000027).
Any neuroblast NB3-5 (FBbt:00001375) that is part of some abdominal segment 7 (FBbt:00000028).
Any neuroblast NB5-2 (FBbt:00001376) that is part of some abdominal segment 7 (FBbt:00000028).
Any neuroblast NB5-3 (FBbt:00001390) that is part of some abdominal segment 7 (FBbt:00000028).
Neuroblast NB5-4 found in abdominal segment 9. It begins to express doublesex in the late embryo, resulting in sexually-dimorphic behavior in the larva (Birkholz et al., 2013). Appears to be two of these on each side in the larva (expressing same markers and generating similar male secondary lineage) - unclear whether this is due to division, migration or if one is a different type of neuroblast (Birkholz et al., 2013).
Neuroblast that generates cells of an abdominal neuromere.
Any neuroblast MNB (FBbt:00001419) that is part of some abdominal segment (FBbt:00000021).
Any neuroblast NB1-2 (FBbt:00001384) that is part of some abdominal segment (FBbt:00000021).
Any neuroblast NB2-1 (FBbt:00001410) that is part of some abdominal segment (FBbt:00000021).
Any neuroblast NB2-5 (FBbt:00001374) that is part of some abdominal segment (FBbt:00000021).
Any neuroblast NB3-2 (FBbt:00001388) that is part of some abdominal segment (FBbt:00000021).
Any neuroblast NB3-3 (FBbt:00001422) that is part of some abdominal segment (FBbt:00000021).
Any neuroblast NB3-4 (FBbt:00001414) that is part of some abdominal segment (FBbt:00000021).
Any neuroblast NB4-1 (FBbt:00001397) that is part of some abdominal segment (FBbt:00000021).
Any neuroblast NB4-2 (FBbt:00001389) that is part of some abdominal segment (FBbt:00000021).
Any neuroblast NB4-3 (FBbt:00001423) that is part of some abdominal segment (FBbt:00000021).
Any neuroblast NB4-4 (FBbt:00001415) that is part of some abdominal segment (FBbt:00000021).
Any neuroblast NB6-1 (FBbt:00001398) that is part of some abdominal segment (FBbt:00000021).
Any neuroblast NB6-2 (FBbt:00001391) that is part of some abdominal segment (FBbt:00000021).
Any neuroblast NB7-1 (FBbt:00001380) that is part of some abdominal segment (FBbt:00000021).
Any neuroblast NB7-2 (FBbt:00001392) that is part of some abdominal segment (FBbt:00000021).
Any neuroblast NB7-4 (FBbt:00001381) that is part of some abdominal segment (FBbt:00000021).
Neuroblast that is the progenitor of interneurons that innervate the antennal lobe.
Neuroblast found in one of abdominal segments 1-7. The pattern of neuroblasts is the same in each of these segments in the embryo (Birkholz et al., 2013; Urbach et al., 2016; Rickert et al., 2018).
A neuroblast located in the anterior region of the protocerebrum. In the embryo, individual neuroblasts are named according to their position relative to major morphological features (cephalic furrow, invaginating foregut, dorsal and ventral midline, their relative position with respect to each other, their time of segregation and their expression of markers) (Urbach et al., 2003).
The most anterior of the three VUM precursors, located posteriorly to the MP3 precursor.
A neuroblast located in the central region of the protocerebrum. In the embryo, individual neuroblasts are named according to their position relative to major morphological features (cephalic furrow, invaginating foregut, dorsal and ventral midline, their relative position with respect to each other, their time of segregation and their expression of markers) (Urbach et al., 2003).
Neuroblast 1 of the dorsal deutocerebrum. It displays serial homology to NB5-3 (Urbach et al., 2016). It delaminates in early embryonic stage 9 (Urbach et al., 2016). Numbering also indicates relative position: we follow the nomenclature of Urbach et al., (2003), in which neuroblasts are numbered from anterior-to-posterior and ventral-to-dorsal (so that numbers reflect relative positions along the dorsoventral axis). Figure 1 of Urbach et al., 2003, provides a survey of the spatial organization of the embryonic head and brain neuroblasts of a stage 11 embryo.
Neuroblast 10 of the dorsal deutocerebrum. Numbering also indicates relative position: we follow the nomenclature of Urbach et al., (2003), in which neuroblasts are numbered from anterior-to-posterior and ventral-to-dorsal (so that numbers reflect relative positions along the dorsoventral axis). Figure 1 of Urbach et al., 2003, provides a survey of the spatial organization of the embryonic head and brain neuroblasts of a stage 11 embryo.
Neuroblast 11 of the dorsal deutocerebrum. Numbering also indicates relative position: we follow the nomenclature of Urbach et al., (2003), in which neuroblasts are numbered from anterior-to-posterior and ventral-to-dorsal (so that numbers reflect relative positions along the dorsoventral axis). Figure 1 of Urbach et al., 2003, provides a survey of the spatial organization of the embryonic head and brain neuroblasts of a stage 11 embryo.
Neuroblast 12 of the dorsal deutocerebrum. Numbering also indicates relative position: we follow the nomenclature of Urbach et al., (2003), in which neuroblasts are numbered from anterior-to-posterior and ventral-to-dorsal (so that numbers reflect relative positions along the dorsoventral axis). Figure 1 of Urbach et al., 2003, provides a survey of the spatial organization of the embryonic head and brain neuroblasts of a stage 11 embryo.
Neuroblast 13 of the dorsal deutocerebrum. Numbering also indicates relative position: we follow the nomenclature of Urbach et al., (2003), in which neuroblasts are numbered from anterior-to-posterior and ventral-to-dorsal (so that numbers reflect relative positions along the dorsoventral axis). Figure 1 of Urbach et al., 2003, provides a survey of the spatial organization of the embryonic head and brain neuroblasts of a stage 11 embryo.
Neuroblast 2 of the dorsal deutocerebrum. Numbering also indicates relative position: we follow the nomenclature of Urbach et al., (2003), in which neuroblasts are numbered from anterior-to-posterior and ventral-to-dorsal (so that numbers reflect relative positions along the dorsoventral axis). Figure 1 of Urbach et al., 2003, provides a survey of the spatial organization of the embryonic head and brain neuroblasts of a stage 11 embryo.
Neuroblast 3 of the dorsal deutocerebrum. It displays serial homology to NB3-3 (Urbach et al., 2016). It delaminates in late embryonic stage 8 (Urbach et al., 2016). Numbering also indicates relative position: we follow the nomenclature of Urbach et al., (2003), in which neuroblasts are numbered from anterior-to-posterior and ventral-to-dorsal (so that numbers reflect relative positions along the dorsoventral axis). Figure 1 of Urbach et al., 2003, provides a survey of the spatial organization of the embryonic head and brain neuroblasts of a stage 11 embryo. Urbach et al. (2016) could not unambiguously assign NB3-3 to either Dd3 or Dd6.
Neuroblast 4 of the dorsal deutocerebrum. It displays serial homology to NB4-4 (Urbach et al., 2016). It delaminates in late embryonic stage 11 (Urbach et al., 2016). Numbering also indicates relative position: we follow the nomenclature of Urbach et al., (2003), in which neuroblasts are numbered from anterior-to-posterior and ventral-to-dorsal (so that numbers reflect relative positions along the dorsoventral axis). Figure 1 of Urbach et al., 2003, provides a survey of the spatial organization of the embryonic head and brain neuroblasts of a stage 11 embryo.
Neuroblast 5 of the dorsal deutocerebrum. It displays serial homology to NB6-2 and NB7-2 (Urbach et al., 2016). It delaminates in late embryonic stage 9 (Urbach et al., 2016). Numbering also indicates relative position: we follow the nomenclature of Urbach et al., (2003), in which neuroblasts are numbered from anterior-to-posterior and ventral-to-dorsal (so that numbers reflect relative positions along the dorsoventral axis). Figure 1 of Urbach et al., 2003, provides a survey of the spatial organization of the embryonic head and brain neuroblasts of a stage 11 embryo.
Neuroblast 6 of the dorsal deutocerebrum. It displays serial homology to NB3-3 (Urbach et al., 2016). It delaminates in late embryonic stage 9 (Urbach et al., 2016). Numbering also indicates relative position: we follow the nomenclature of Urbach et al., (2003), in which neuroblasts are numbered from anterior-to-posterior and ventral-to-dorsal (so that numbers reflect relative positions along the dorsoventral axis). Figure 1 of Urbach et al., 2003, provides a survey of the spatial organization of the embryonic head and brain neuroblasts of a stage 11 embryo. Urbach et al. (2016) could not unambiguously assign NB3-3 to either Dd3 or Dd6.
Neuroblast 7 of the dorsal deutocerebrum. It displays serial homology to NB5-6 (Urbach et al., 2016). It delaminates in early embryonic stage 9 (Urbach et al., 2016). Numbering also indicates relative position: we follow the nomenclature of Urbach et al., (2003), in which neuroblasts are numbered from anterior-to-posterior and ventral-to-dorsal (so that numbers reflect relative positions along the dorsoventral axis). Figure 1 of Urbach et al., 2003, provides a survey of the spatial organization of the embryonic head and brain neuroblasts of a stage 11 embryo.
Neuroblast 8 of the dorsal deutocerebrum. It displays serial homology to NB3-5 (Urbach et al., 2016). It delaminates in late embryonic stage 8 (Urbach et al., 2016). Numbering also indicates relative position: we follow the nomenclature of Urbach et al., (2003), in which neuroblasts are numbered from anterior-to-posterior and ventral-to-dorsal (so that numbers reflect relative positions along the dorsoventral axis). Figure 1 of Urbach et al., 2003, provides a survey of the spatial organization of the embryonic head and brain neuroblasts of a stage 11 embryo.
Neuroblast 9 of the dorsal deutocerebrum. Numbering also indicates relative position: we follow the nomenclature of Urbach et al., (2003), in which neuroblasts are numbered from anterior-to-posterior and ventral-to-dorsal (so that numbers reflect relative positions along the dorsoventral axis). Figure 1 of Urbach et al., 2003, provides a survey of the spatial organization of the embryonic head and brain neuroblasts of a stage 11 embryo.
A neuroblast located in the deutocerebrum. Some of these are serial homologues of neuroblasts found in the thoracic neuromeres (Urbach et al., 2016). In the embryo, individual neuroblasts are named according to their position relative to major morphological features (cephalic furrow, invaginating foregut, dorsal and ventral midline, their relative position with respect to each other, their time of segregation and their expression of markers) (Urbach et al., 2003).
First intermediate neural progenitor to be born from neuroblast DM5 during the post-embryonic stage (Ren et al., 2016).
First intermediate neural progenitor to be born from neuroblast DM6 during the post-embryonic stage (Ren et al., 2016).
A neuroblast located in the dorsal region of the anterior protocerebrum.
A neuroblast located in the dorsal region of the central protocerebrum. In the embryo, individual neuroblasts are named according to their position relative to major morphological features (cephalic furrow, invaginating foregut, dorsal and ventral midline, their relative position with respect to each other, their time of segregation and their expression of markers) (Urbach et al., 2003).
A neuroblast located in the dorsal region of the deutocerebrum. In the embryo, individual neuroblasts are named according to their position relative to major morphological features (cephalic furrow, invaginating foregut, dorsal and ventral midline, their relative position with respect to each other, their time of segregation and their expression of markers) (Urbach et al., 2003).
A neuroblast located in the dorsal region of the posterior protocerebrum. In the embryo, individual neuroblasts are named according to their position relative to major morphological features (cephalic furrow, invaginating foregut, dorsal and ventral midline, their relative position with respect to each other, their time of segregation and their expression of markers) (Urbach et al., 2003).
A neuroblast located in the dorsal region of the tritocerebrum. In the embryo, individual neuroblasts are named according to their position relative to major morphological features (cephalic furrow, invaginating foregut, dorsal and ventral midline, their relative position with respect to each other, their time of segregation and their expression of markers) (Urbach et al., 2003).
Neuroblast 1 of the ventral deutocerebrum. Numbering also indicates relative position: we follow the nomenclature of Urbach et al., (2003), in which neuroblasts are numbered from anterior-to-posterior and ventral-to-dorsal (so that numbers reflect relative positions along the dorsoventral axis). Figure 1 of Urbach et al., 2003, provides a survey of the spatial organization of the embryonic head and brain neuroblasts of a stage 11 embryo.
Neuroblast 2 of the ventral deutocerebrum. Numbering also indicates relative position: we follow the nomenclature of Urbach et al., (2003), in which neuroblasts are numbered from anterior-to-posterior and ventral-to-dorsal (so that numbers reflect relative positions along the dorsoventral axis). Figure 1 of Urbach et al., 2003, provides a survey of the spatial organization of the embryonic head and brain neuroblasts of a stage 11 embryo.
Neuroblast 3 of the ventral deutocerebrum. Numbering also indicates relative position: we follow the nomenclature of Urbach et al., (2003), in which neuroblasts are numbered from anterior-to-posterior and ventral-to-dorsal (so that numbers reflect relative positions along the dorsoventral axis). Figure 1 of Urbach et al., 2003, provides a survey of the spatial organization of the embryonic head and brain neuroblasts of a stage 11 embryo.
Neuroblast 4 of the ventral deutocerebrum. Numbering also indicates relative position: we follow the nomenclature of Urbach et al., (2003), in which neuroblasts are numbered from anterior-to-posterior and ventral-to-dorsal (so that numbers reflect relative positions along the dorsoventral axis). Figure 1 of Urbach et al., 2003, provides a survey of the spatial organization of the embryonic head and brain neuroblasts of a stage 11 embryo.
Neuroblast 5 of the ventral deutocerebrum. Numbering also indicates relative position: we follow the nomenclature of Urbach et al., (2003), in which neuroblasts are numbered from anterior-to-posterior and ventral-to-dorsal (so that numbers reflect relative positions along the dorsoventral axis). Figure 1 of Urbach et al., 2003, provides a survey of the spatial organization of the embryonic head and brain neuroblasts of a stage 11 embryo.
Neuroblast 6 of the ventral deutocerebrum. It displays serial homology to NB3-2 and NB4-2 (Urbach et al., 2016). It delaminates in early embryonic stage 9 (Urbach et al., 2016). Numbering also indicates relative position: we follow the nomenclature of Urbach et al., (2003), in which neuroblasts are numbered from anterior-to-posterior and ventral-to-dorsal (so that numbers reflect relative positions along the dorsoventral axis). Figure 1 of Urbach et al., 2003, provides a survey of the spatial organization of the embryonic head and brain neuroblasts of a stage 11 embryo.
Neuroblast 7 of the ventral deutocerebrum. Numbering also indicates relative position: we follow the nomenclature of Urbach et al., (2003), in which neuroblasts are numbered from anterior-to-posterior and ventral-to-dorsal (so that numbers reflect relative positions along the dorsoventral axis). Figure 1 of Urbach et al., 2003, provides a survey of the spatial organization of the embryonic head and brain neuroblasts of a stage 11 embryo.
Neuroblast 8 of the ventral deutocerebrum. It displays serial homology to NB1-2 (Urbach et al., 2016). It delaminates in early embryonic stage 10 (Urbach et al., 2016). Numbering also indicates relative position: we follow the nomenclature of Urbach et al., (2003), in which neuroblasts are numbered from anterior-to-posterior and ventral-to-dorsal (so that numbers reflect relative positions along the dorsoventral axis). Figure 1 of Urbach et al., 2003, provides a survey of the spatial organization of the embryonic head and brain neuroblasts of a stage 11 embryo.
Any neuroblast (FBbt:00005146) that is part of some embryo (FBbt:00000052).
Neuroblast of the embryonic optic lobe that arises from the neuroepithelium. They are produced continuously between stage 12 and stage 17, with a final number of around 8 or 9 per brain lobe. They express similar markers to larval neuroblasts and produce neurons and glia during embryogenesis. They enter G0 quiescence prior to larval hatching and persist into the larval stage, they are among the last neuroblasts in the larval brain to reactivate (Hakes et al., 2018).
Neuroblast that is a precursor to the larval ventral midline neurons, which are found in the ventralmost part of the ventral nerve cord (Kearney et al., 2004). There are four of these cells per neuromere (Kearney et al., 2004).
A neuroblast located in one of the three gnathal neuromeres. These are all homologues of neuroblasts in the thoracic neuromeres (Urbach et al., 2016)
A neuroblast located in the larval inner optic anlage that will give rise to the adult inner medulla, lobula and lobula plate neurons. It develops from a neuroepithelial cell in the medial region of the inner optic anlage.
Any neuroblast MNB (FBbt:00001419) that is part of some labial segment (FBbt:00000014).
Any neuroblast NB1-1 (FBbt:00001371) that is part of some labial segment (FBbt:00000014).
Any neuroblast NB1-2 (FBbt:00001384) that is part of some labial segment (FBbt:00000014).
Any neuroblast NB2-1 (FBbt:00001410) that is part of some labial segment (FBbt:00000014).
Any neuroblast NB2-2 (FBbt:00001385) that is part of some labial segment (FBbt:00000014).
Any neuroblast NB2-5 (FBbt:00001374) that is part of some labial segment (FBbt:00000014).
Any neuroblast NB3-1 (FBbt:00001394) that is part of some labial segment (FBbt:00000014).
Any neuroblast NB3-2 (FBbt:00001388) that is part of some labial segment (FBbt:00000014).
Any neuroblast NB3-3 (FBbt:00001422) that is part of some labial segment (FBbt:00000014).
Any neuroblast NB3-4 (FBbt:00001414) that is part of some labial segment (FBbt:00000014).
Any neuroblast NB3-5 (FBbt:00001375) that is part of some labial segment (FBbt:00000014).
Any neuroblast NB4-1 (FBbt:00001397) that is part of some labial segment (FBbt:00000014).
Any neuroblast NB4-2 (FBbt:00001389) that is part of some labial segment (FBbt:00000014).
Any neuroblast NB4-3 (FBbt:00001423) that is part of some labial segment (FBbt:00000014).
Any neuroblast NB4-4 (FBbt:00001415) that is part of some labial segment (FBbt:00000014).
Any neuroblast NB5-1 (FBbt:00001424) that is part of some labial segment (FBbt:00000014).
Any neuroblast NB5-2 (FBbt:00001376) that is part of some labial segment (FBbt:00000014).
Any neuroblast NB5-3 (FBbt:00001390) that is part of some labial segment (FBbt:00000014).
Any neuroblast NB5-4 (FBbt:00001416) that is part of some labial segment (FBbt:00000014).
Neuroblast NB5-6 found in a labial segment. Uniquely among NB5-6 neuroblasts, the labial NB5-6 produces a primary neuron with an ascending projection (Rickert et al., 2018). Unlike more posterior NB5-6 neuroblasts, it survives into the larva and produces a secondary lineage (Lacin and Truman, 2016).
Any neuroblast NB6-1 (FBbt:00001398) that is part of some labial segment (FBbt:00000014).
Any neuroblast NB6-2 (FBbt:00001391) that is part of some labial segment (FBbt:00000014).
Neuroblast NB6-4 found in a labial segment. Its first division produces a daughter cell that generates only glia and a daughter cell that produces ganglion mother cells that give rise to neurons (Becker et al., 2016). It does not produce a secondary lineage (Lacin and Truman, 2016).
Any neuroblast NB7-1 (FBbt:00001380) that is part of some labial segment (FBbt:00000014).
Any neuroblast NB7-2 (FBbt:00001392) that is part of some labial segment (FBbt:00000014).
Any neuroblast NB7-3 (FBbt:00001426) that is part of some labial segment (FBbt:00000014).
Any neuroblast NB7-4 (FBbt:00001381) that is part of some labial segment (FBbt:00000014).
A neuroblast that is the precursor of the lamina. The neuroblasts that give rise to the lamina neurons are located in the lateral edge of the larval outer optic anlage.
Neuroblast NB5-4 found in female abdominal segment 9 at the larval stage. It begins to express doublesex in the late embryo, then undergoes programmed cell death in the early larva without producing a secondary lineage (Birkholz et al., 2013).
Neuroblast NB5-4 found in male abdominal segment 9 at the larval stage. It begins to express doublesex in the late embryo, and proliferates to generate a male-specific secondary lineage (Birkholz et al., 2013).
Any neuroblast (FBbt:00005146) that is part of some larva (FBbt:00001727).
Neuroblast found in a terminal abdominal neuromere of the larval ventral nerve cord that exits quiescence in early larval stages (Ghosh et al., 2019). There are 12 of these cells, four of which express doublesex (Ghosh et al., 2019). In females, doublesex-positive neuroblasts die during larval stages (Ghosh et al., 2019).
A neuroblast that is the precursor of the lobula. The neuroblasts that give rise to the lobula neurons are located in the larval inner optic anlage.
Any neuroblast MNB (FBbt:00001419) that is part of some mandibular segment (FBbt:00000012).
Neuroblast MP2 of a mandibular segment, unlike in other segments, there are three of these on each side (Urbach et al., 2016).
Any neuroblast NB2-1 (FBbt:00001410) that is part of some mandibular segment (FBbt:00000012).
Any neuroblast NB2-2 (FBbt:00001385) that is part of some mandibular segment (FBbt:00000012).
Any neuroblast NB2-5 (FBbt:00001374) that is part of some mandibular segment (FBbt:00000012).
Any neuroblast NB3-1 (FBbt:00001394) that is part of some mandibular segment (FBbt:00000012).
Any neuroblast NB3-4 (FBbt:00001414) that is part of some mandibular segment (FBbt:00000012).
Any neuroblast NB3-5 (FBbt:00001375) that is part of some mandibular segment (FBbt:00000012).
Any neuroblast NB4-1 (FBbt:00001397) that is part of some mandibular segment (FBbt:00000012).
Any neuroblast NB4-2 (FBbt:00001389) that is part of some mandibular segment (FBbt:00000012).
Any neuroblast NB4-3 (FBbt:00001423) that is part of some mandibular segment (FBbt:00000012).
Any neuroblast NB4-4 (FBbt:00001415) that is part of some mandibular segment (FBbt:00000012).
Any neuroblast NB5-3 (FBbt:00001390) that is part of some mandibular segment (FBbt:00000012).
Any neuroblast NB5-6 (FBbt:00001377) that is part of some mandibular segment (FBbt:00000012).
Any neuroblast NB6-1 (FBbt:00001398) that is part of some mandibular segment (FBbt:00000012).
Neuroblast NB6-2 found in a mandibular neuromere, it produces a notably smaller primary lineage compared to more posterior NB6-2 cells (Rickert et al., 2018).
Any neuroblast NB7-1 (FBbt:00001380) that is part of some mandibular segment (FBbt:00000012).
Any neuroblast NB7-2 (FBbt:00001392) that is part of some mandibular segment (FBbt:00000012).
Any neuroblast NB7-3 (FBbt:00001426) that is part of some mandibular segment (FBbt:00000012).
Any neuroblast NB7-4 (FBbt:00001381) that is part of some mandibular segment (FBbt:00000012).
Any neuroblast MNB (FBbt:00001419) that is part of some maxillary segment (FBbt:00000013).
Any neuroblast NB1-1 (FBbt:00001371) that is part of some maxillary segment (FBbt:00000013).
Any neuroblast NB1-2 (FBbt:00001384) that is part of some maxillary segment (FBbt:00000013).
Any neuroblast NB2-1 (FBbt:00001410) that is part of some maxillary segment (FBbt:00000013).
Any neuroblast NB2-2 (FBbt:00001385) that is part of some maxillary segment (FBbt:00000013).
Any neuroblast NB2-5 (FBbt:00001374) that is part of some maxillary segment (FBbt:00000013).
Any neuroblast NB3-1 (FBbt:00001394) that is part of some maxillary segment (FBbt:00000013).
Any neuroblast NB3-2 (FBbt:00001388) that is part of some maxillary segment (FBbt:00000013).
Any neuroblast NB3-3 (FBbt:00001422) that is part of some maxillary segment (FBbt:00000013).
Any neuroblast NB3-4 (FBbt:00001414) that is part of some maxillary segment (FBbt:00000013).
Any neuroblast NB3-5 (FBbt:00001375) that is part of some maxillary segment (FBbt:00000013).
Any neuroblast NB4-1 (FBbt:00001397) that is part of some maxillary segment (FBbt:00000013).
Any neuroblast NB4-2 (FBbt:00001389) that is part of some maxillary segment (FBbt:00000013).
Any neuroblast NB4-3 (FBbt:00001423) that is part of some maxillary segment (FBbt:00000013).
Any neuroblast NB4-4 (FBbt:00001415) that is part of some maxillary segment (FBbt:00000013).
Any neuroblast NB5-1 (FBbt:00001424) that is part of some maxillary segment (FBbt:00000013).
Any neuroblast NB5-2 (FBbt:00001376) that is part of some maxillary segment (FBbt:00000013).
Any neuroblast NB5-3 (FBbt:00001390) that is part of some maxillary segment (FBbt:00000013).
Any neuroblast NB5-6 (FBbt:00001377) that is part of some maxillary segment (FBbt:00000013).
Any neuroblast NB6-1 (FBbt:00001398) that is part of some maxillary segment (FBbt:00000013).
Any neuroblast NB6-2 (FBbt:00001391) that is part of some maxillary segment (FBbt:00000013).
Neuroblast NB6-4 found in a maxillary segment. It only produces glia (Becker et al., 2016).
Any neuroblast NB7-1 (FBbt:00001380) that is part of some maxillary segment (FBbt:00000013).
Any neuroblast NB7-2 (FBbt:00001392) that is part of some maxillary segment (FBbt:00000013).
Any neuroblast NB7-3 (FBbt:00001426) that is part of some maxillary segment (FBbt:00000013).
Any neuroblast NB7-4 (FBbt:00001381) that is part of some maxillary segment (FBbt:00000013).
A neuroblast that is the precursor of the medulla. The neuroblasts that give rise to the outer medulla neurons are located in the medial edge of the larval outer optic anlage, whereas the neuroblasts that give rise to the inner medulla neurons are located in the larval inner optic anlage.
Any neuroblast NB3-5 (FBbt:00001375) that is part of some mesothoracic segment (FBbt:00000018).
Any neuroblast NB5-2 (FBbt:00001376) that is part of some mesothoracic segment (FBbt:00000018).
Any neuroblast NB5-3 (FBbt:00001390) that is part of some mesothoracic segment (FBbt:00000018).
Any neuroblast NB7-2 (FBbt:00001392) that is part of some mesothoracic segment (FBbt:00000018).
Any neuroblast NB3-5 (FBbt:00001375) that is part of some metathoracic segment (FBbt:00000019).
Any neuroblast NB5-2 (FBbt:00001376) that is part of some metathoracic segment (FBbt:00000019).
Any neuroblast NB5-3 (FBbt:00001390) that is part of some metathoracic segment (FBbt:00000019).
Any neuroblast NB7-2 (FBbt:00001392) that is part of some metathoracic segment (FBbt:00000019).
The middle of the three VUM precursors, located in between the anterior and posterior VUM precursors.
Neuroblast found on the midline of the ventral nervous system that is not part of a bilateral pair and generates unpaired neurons. This includes the midline precursor (MP) cells and the median neuroblast (MNB) (Fontana and Crews, 2012).
Unpaired precursor cell that divides once, during embryonic development, to produce two MP1 interneurons.
Midline precursor neuron of the ventral nerve cord posterior to MP1 precursor. It divides once, during embryonic development, to give rise to the interneurons H-cell and the H-cell sib.
Neuroblast that is the precursor to the Kenyon cells (Kunz et al., 2012). There are four of these per hemisphere and they each arise from a distinct neuroectodermal progenitor and produce morphologically distinct primary lineages (Kunz et al., 2012). They continue to divide from the embryonic to the late pupal stage (Lee et al., 1999; Kunz et al., 2012). All four produce largely identical lineages postembryonically (Ito et al., 2013; Yu et al., 2013), sequentially producing gamma, alpha’/beta’ and alpha/beta Kenyon cells (Lee et al., 1999; Kunz et al., 2012). In the adult, each lineage remains distinct within the calyx and pedunculus, but the axons reorganize and intermingle within the lobes (Li et al., 2020). See Ito et al. (2013) figure S1 for distinction between MBp1-4.
Neuroblast that generates three types of antennal lobe projection neuron; uniglomerular, biglomerular and multiglomerular, which all tend to send axons to glomeruli of the mushroom body calyx (Das et al., 2013). The neurons have cell bodies on the anterior-dorsal surface of the antennal lobe in the adult (Jefferis et al., 2001; Yu et al., 2013).
Neuroblast that generates antennal lobe neurons with laterally-located cell bodies in the adult (Jefferis et al., 2001; Yu et al., 2013). It skips the quiescent period beginning in late embryogenesis and produces a large number of neurons (200 or more) (Yu et al., 2013). It produces various multiglomerular and oligoglomerular primary local interneurons, many of which also project to the neighboring subesophageal neuropil (Das et al., 2013). Eckstein et al. (2020) - doi:10.1101/2020.06.12.148775 map dorsal and ventral hemilineages of ALl1 to dorsal and ventral hemilineages of BAlc.
Tritocerebral neuroblast (Kuert et al., 2014) that generates primary and secondary olfactory projection neurons that innervate part of the posterior antennal lobe, the adjacent gnathal ganglion and higher brain centers other than the mushroom body calyx and the lateral horn (Das et al., 2013).
Neuroblast that generates antennal lobe projection neurons with cell bodies in a cluster found ventral to the antennal lobe in the adult (Jefferis et al., 2001; Yu et al., 2013). This lineage mainly generates neurons with only short branches into the antennal lobe and more extensive ones into the adjacent basal brain compartments posterior to the antennal lobe. It also generates a few oligoglomerular and multiglomerular primary projection neurons (Das et al., 2013). Some neurons of this lineage, referred to as extra-antennal BAla1 projection neurons, do not enter the antennal lobe (Das et al., 2013).
Neuroblast that generates primary local interneurons of diverse multiglomerular and oligoglomerular types (Das et al., 2013). These neurons have their cell bodies in a cluster of the ventral side of the antennal lobe in the adult (Yu et al., 2013).
Basoanterior neuroblast (Pereanu and Hartenstein, 2006). In the larva, these neuroblasts are located around the antennal compartment (Pereanu et al., 2006). Some of these form the ventral deutocerebrum and two are tritocerebral (Pereanu and Hartenstein, 2006; Kuert et al., 2012).
. The existence of this neuroblast is inferred from lineage data (Pereanu and Hartenstein, 2006). This paper studies secondary neuroblast divisions. Although all of these lineages will correspond to a lineage from a known primary neuroblast lineage, only some will correspond to lineages from the secondary neuroblast division.
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. ‘BAlp2 dorsal’ mapped to ’new2 ventral’ in Bates et al. (2020) - FlyBase:FBrf0246460.
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Neuroblast of the tritocerebrum that generates a secondary lineage (Kuert et al., 2014). Eckstein et al. (2020) - doi:10.1101/2020.06.12.148775 map dorsal and ventral hemilineages of WEDa1 to BAlv.
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Neuroblast of the brain that generates a sexually-dimorphic lineage with prominent proximal neurite elaboration in the flange (Yu et al., 2013).
Any neuroblast BAmas2 (FBbt:00100556) that is part of some female organism (FBbt:00007011).
Any neuroblast BAmas2 (FBbt:00100556) that is part of some male organism (FBbt:00007004).
. Eckstein et al. (2020) - doi:10.1101/2020.06.12.148775 map the ventral hemilineage of CREa1 to the ventral hemilineage of BAMd1.
. The existence of this neuroblast is inferred from lineage data (Pereanu and Hartenstein, 2006). This paper studies secondary neuroblast divisions. Although all of these lineages will correspond to a lineage from a known primary neuroblast lineage, only some will correspond to lineages from the secondary neuroblast division. Might be the same as neuroblast WEDd2 (Wong et al., 2013 - FBrf0223298).
. The existence of this neuroblast is inferred from lineage data (Pereanu and Hartenstein, 2006). This paper studies secondary neuroblast divisions. Although all of these lineages will correspond to a lineage from a known primary neuroblast lineage, only some will correspond to lineages from the secondary neuroblast division.
Neuroblast located anterior to the outer optic anlage, lateral to the spur of the mushroom body (Pereanu and Hartenstein, 2006).
. Eckstein et al. (2020) - doi:10.1101/2020.06.12.148775 map the medial hemilineage of LHa1 to the medial hemilineage of BLAd1.
. Eckstein et al. (2020) - doi:10.1101/2020.06.12.148775 map dorsal and ventral hemilineages of BLAd2 to dorsal and ventral hemilineages of SIPa1.
. Eckstein et al. (2020) - doi:10.1101/2020.06.12.148775 map the dorsal hemilineage of SLPal3 to the dorsal hemilineage of BLAd3.
. The existence of this neuroblast is inferred from lineage data (Pereanu and Hartenstein, 2006). This paper studies secondary neuroblast divisions. Although all of these lineages will correspond to a lineage from a known primary neuroblast lineage, only some will correspond to lineages from the secondary neuroblast division.
. BLAl lateral hemilineage mapped to SLPa&l1 lateral hemilineage and SLPav1 lateral hemilineage in Eckstein et al. (2020) - doi:10.1101/2020.06.12.148775.
. Eckstein et al. (2020) - doi:10.1101/2020.06.12.148775 map lateral and dorsal hemilineages of VLPl&d1 to lateral and dorsal hemilineages of BLAv1.
. Eckstein et al. (2020) - doi:10.1101/2020.06.12.148775) map dorsal and ventral hemilineages of VLPl2 to dorsal and ventral hemilineages of BLAv2.
. BLAvm1 anterior hemilineage mapped to SLPa&l1 anterior hemilineage in Eckstein et al. (2020) - doi:10.1101/2020.06.12.148775, but SLPa&l1 lateral mapped to BLAl lateral.
Neuroblast located dorsally of the optic lobe (Pereanu and Hartenstein, 2006).
Most anterior neuroblast in the BLD group (Pereanu and Hartenstein, 2006). It has descendants that enter the superior lateral protocerebrum and join the intermediate superior transverse fascicle (Lovick et al., 2013; Hartenstein et al., 2015). At the secondary stage, one hemilineage continues to follow this route and another follows a more ventrally-directed tract along the surface of the posterior ventrolateral protocerebrum (Lovick et al., 2013). Eckstein et al. (2020) - doi:10.1101/2020.06.12.148775 map lateral and posterior hemilineages of LHl4 to lateral and posterior hemilineages of BLD1.
Neuroblast with a relatively anterior position in the BLD group (Pereanu and Hartenstein, 2006). It has descendants that enter the superior lateral protocerebrum and join the intermediate superior transverse fascicle (Lovick et al., 2013; Hartenstein et al., 2015). Eckstein et al. (2020) - doi:10.1101/2020.06.12.148775 map the dorsal hemilineage of SLPav2 to the dorsal hemilineage of BLD2.
Neuroblast with a relatively anterior position in the BLD group (Pereanu and Hartenstein, 2006). It has descendants that enter the superior lateral protocerebrum and join the intermediate superior transverse fascicle (Lovick et al., 2013; Hartenstein et al., 2015). At the secondary stage, one hemilineage continues to follow this route and another follows a more ventrally-directed tract (Lovick et al., 2013).
Neuroblast with a relatively anterior position in the BLD group (Pereanu and Hartenstein, 2006). It has descendants that enter the superior lateral protocerebrum and join the intermediate superior transverse fascicle (Lovick et al., 2013; Hartenstein et al., 2015). At the secondary stage, one hemilineage continues to follow this route and another follows a more ventrally-directed tract that reaches the anterior ventrolateral protocerebrum (Lovick et al., 2013). Eckstein et al. (2020) - doi:10.1101/2020.06.12.148775 map the lateral hemilineage of LHl1 to the lateral hemilineage of BLD4.
Neuroblast with a relatively posterior position in the BLD group, close to BLD5 (VPNp1) (Wong et al., 2013).
Neuroblast flanking the posterior side of the optic lobe (Pereanu and Hartenstein, 2006).
. Eckstein et al. (2020) - doi:10.1101/2020.06.12.148775 map the posterior hemilineage of VPNp&v1 to the posterior hemilineage of BLP1.
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. ‘BLP3 ventral’ mapped to ‘unknown6 ventral’ in Bates et al. (2020) - FlyBase:FBrf0246460.
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. The existence of this neuroblast is inferred from lineage data (Pereanu and Hartenstein, 2006). This paper studies secondary neuroblast divisions. Although all of these lineages will correspond to a lineage from a known primary neuroblast lineage, only some will correspond to lineages from the secondary neuroblast division.
Neuroblast that is located medially adjacent to the outer optic anlage in the larval stage (Pereanu and Hartenstein, 2006). Its lineages remain lateral relative to the central brain into the adult stage, although some shift dorsally or anteriorly (Lovick et al., 2013).
Neuroblast that forms a paired lineage with BLVa2 (Lovick et al., 2013; Wong et al., 2013; Hartenstein et al., 2015). Their descendants follow a longer fiber tract that those of BLVa3/4 that projects dorsally, entering the ventrolateral protocerebrum at the base of the lateral horn (Lovick et al., 2013; Wong et al., 2013; Hartenstein et al., 2015). Their cell body clusters shift dorsally during late pupal stages (Lovick et al., 2013). Eckstein et al. (2020) - doi:10.1101/2020.06.12.148775 map dorsal and ventral hemilineages of LHa2 to dorsal and ventral hemilineages of BLVa1.
Neuroblast that forms a paired lineage with BLVa1 (Lovick et al., 2013; Wong et al., 2013; Hartenstein et al., 2015). Their descendants follow a longer fiber tract that those of BLVa3/4 that projects dorsally, entering the ventrolateral protocerebrum at the base of the lateral horn (Lovick et al., 2013; Wong et al., 2013; Hartenstein et al., 2015). Their cell body clusters shift dorsally during late pupal stages (Lovick et al., 2013). Suggested to be equivalent to neuroblast LHa4 in Hartenstein et al. (2017) - FBrf0234128, but BLVa2 mapped to LHa3 in Bates et al. (2020) - FlyBase:FBrf0246460 and Eckstein et al. (2020) - doi:10.1101/2020.06.12.148775 (and BLVa2a mapped to SLPav3).
Neuroblast that forms a paired lineage with BLVa4 (Lovick et al., 2013; Wong et al., 2013; Hartenstein et al., 2015). Their descendants follow a short tract that projects dorsally into the ventrolateral protocerebrum (Lovick et al., 2013; Wong et al., 2013; Hartenstein et al., 2015). VLPl1 mapped to BLVa3/4 in Eckstein et al. (2020) - doi:10.1101/2020.06.12.148775.
Neuroblast that forms a paired lineage with BLVa3 (Lovick et al., 2013; Wong et al., 2013; Hartenstein et al., 2015). Their descendants follow a short tract that projects dorsally into the ventrolateral protocerebrum (Lovick et al., 2013; Wong et al., 2013; Hartenstein et al., 2015). VLPl1 mapped to BLVa3/4 in Eckstein et al. (2020) - doi:10.1101/2020.06.12.148775.
Neuroblast that is relatively posteriorly-located in the BLV group, close to BLVp2 (Pereanu and Hartenstein, 2006; Lovick et al., 2013; Hartenstein et al., 2015). It produces two hemilineages that migrate apart at metamorphosis (Lovick et al., 2013; Wong et al., 2013). The BLVp1/2 of Pereanu and Hartenstein (2006) may be branches/hemilineages of BLVp1 (Cardona et al., 2010; Lovick et al., 2013 Wong et al., 2013). Eckstein et al. (2020) - doi:10.1101/2020.06.12.148775 map the posterior hemilineage of VLPl&p2 to the posterior hemilineage of BLVp1.
Neuroblast that is relatively posteriorly-located in the BLV group, close to BLVp1 (Lovick et al., 2013; Hartenstein et al., 2015). It produces two hemilineages that migrate apart at metamorphosis (Lovick et al., 2013; Wong et al., 2013). The BLVp3/4 of Pereanu and Hartenstein (2006) (FBrf0194268) may be branches/hemilineages of BLVp2 (Cardona et al., 2010; Lovick et al., 2013 Wong et al., 2013). Referred to as BLVp3 in the larva by Cardona et al. (2010) (Lovick et al., 2013). Eckstein et al. (2020) - doi:10.1101/2020.06.12.148775 map anterior and posterior hemilineages of VLPl&p1 to anterior and posterior hemilineages of BLVp2.
. CLp1 mapped to DPLc2/4 in Eckstein et al. (2020) - doi:10.1101/2020.06.12.148775.
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Centromedial neuroblast located in the posterior deutocerebrum (Pereanu and Hartenstein, 2006).
A type II centromedial neuroblast of the posterior deutocerebrum. The existence of this neuroblast is inferred from lineage data (Pereanu and Hartenstein, 2006). This paper studies secondary neuroblast divisions. Although all of these lineages will correspond to a lineage from a known primary neuroblast lineage, only some will correspond to lineages from the secondary neuroblast division.
A type II centromedial neuroblast of the posterior deutocerebrum. The existence of this neuroblast is inferred from lineage data (Pereanu and Hartenstein, 2006). This paper studies secondary neuroblast divisions. Although all of these lineages will correspond to a lineage from a known primary neuroblast lineage, only some will correspond to lineages from the secondary neuroblast division.
Neuroblast located over the posterior apex of the brain.
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. Eckstein et al. (2020) - doi:10.1101/2020.06.12.148775 map dorsal and ventral hemilineages of DL1 to dorsal and ventral hemilineages of CP2.
. Eckstein et al. (2020) - doi:10.1101/2020.06.12.148775 map dorsal and ventral hemilineages of DL2 to dorsal and ventral hemilineages of CP3.
. The existence of this neuroblast is inferred from lineage data (Pereanu and Hartenstein, 2006). This paper studies secondary neuroblast divisions. Although all of these lineages will correspond to a lineage from a known primary neuroblast lineage, only some will correspond to lineages from the secondary neuroblast division.
Type I neuroblast of the brain that produces a secondary lineage with somas posterolateral to the lateral horn and arbors in the lateral horn and posterior superior protocerebrum (Schlegel et al., 2023).
Neuroblast of the brain that generates a sexually-dimorphic lineage with prominent proximal neurite elaboration in the crepine (Yu et al., 2013). Eckstein et al. (2020) - doi:10.1101/2020.06.12.148775 map the ventral hemilineage of CREa1 to the ventral hemilineage of BAMd1.
Any neuroblast CREa1 (FBbt:00049462) that is part of some female organism (FBbt:00007011).
Any neuroblast CREa1 (FBbt:00049462) that is part of some male organism (FBbt:00007004).
Dorsoanterior lateral neuroblast. In the larva, this group of neuroblasts is found flanking the spur and the dorsal lobe of the mushroom body anteriorly and laterally (Pereanu and Hartenstein, 2006).
. Eckstein et al. (2020) - doi:10.1101/2020.06.12.148775 map dorsal and ventral hemilineages of DALcl1 to dorsal and ventral hemilineages of AOTUv3.
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Neuroblast with a relatively dorsal location within the DAL group (Pereanu and Hartenstein, 2006), lateral to the mushroom body vertical lobe (Lovick et al., 2013; Hartenstein et al., 2015). It produces neurons that descend from the protocerebrum to the ventral brain (Lovick et al., 2013; Hartenstein et al., 2015).
Neuroblast found lateral to the DALcl and DALv groups (Pereanu and Hartenstein, 2006; Lovick et al., 2013; Wong et al., 2013; Hartenstein et al., 2015). Its descendants enter the ventrolateral protocerebrum, with secondary neurons having a characteristic trajectory along the lateral surface of the peduncle and then backward to the anterior anterior optic tubercle (Lovick et al., 2013; Hartenstein et al., 2015).
Neuroblast found lateral to the DALcl and DALv groups (Pereanu and Hartenstein, 2006; Lovick et al., 2013; Wong et al., 2013; Hartenstein et al., 2015). Its descendants enter the ventrolateral protocerebrum (Lovick et al., 2013; Hartenstein et al., 2015).
. The existence of this neuroblast is inferred from lineage data (Pereanu and Hartenstein, 2006). This paper studies secondary neuroblast divisions. Although all of these lineages will correspond to a lineage from a known primary neuroblast lineage, only some will correspond to lineages from the secondary neuroblast division. Might be the same as neuroblast VLPa2 (Wong et al., 2013 - FBrf0223298).
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Ventral DAL neuroblast. It is part of the deutocerebrum (Pereanu and Hartenstein, 2006). The existence of this neuroblast is inferred from lineage data (Pereanu and Hartenstein, 2006). This paper studies secondary neuroblast divisions. Although all of these lineages will correspond to a lineage from a known primary neuroblast lineage, only some will correspond to lineages from the secondary neuroblast division. Bridi et al. (2019) - FlyBase:FBrf0243005 suggest that Ppd5 corresponds to EBa1/p1 and DALv2/3.
Dorsoanterior medial neuroblast. In the larva, it is located anterior and medial of the mushroom body (Pereanu and Hartenstein, 2006).
Neuroblast that is relatively dorsal within the DAM group (Pereanu and Hartenstein, 2006). Its lineage follows a medially-projecting tract that crosses the midline (Pereanu and Hartenstein, 2006; Lovick et al., 2013; Wong et al., 2013; Hartenstein et al., 2015).
Neuroblast located relatively dorsally within the DAM group (Pereanu and Hartenstein, 2006). Similar to DAMd3, it generates a large lineage that follows a posteriorly-projecting tract (Wong et al., 2013; Hartenstein et al., 2015). SMPad2 mapped to DAMd2/3 in Eckstein et al. (2020) - doi:10.1101/2020.06.12.148775.
Neuroblast located relatively dorsally within the DAM group (Pereanu and Hartenstein, 2006). Similar to DAMd2, it generates a large lineage that follows a posteriorly-projecting tract (Wong et al., 2013; Hartenstein et al., 2015). SMPad2 mapped to DAMd2/3 in Eckstein et al. (2020) - doi:10.1101/2020.06.12.148775.
Neuroblast located relatively ventrally within the DAM group (Pereanu and Hartenstein, 2006). Similar to DAMv2, its lineage forms a short dorsoposteriorly-projecting tract into the superior medial protocerebrum (Lovick et al., 2013; Wong et al., 2013; Hartenstein et al., 2015).
Neuroblast located relatively ventrally within the DAM group (Pereanu and Hartenstein, 2006). Similar to DAMv3, its lineage forms a short dorsoposteriorly-projecting tract into the superior medial protocerebrum (Lovick et al., 2013; Wong et al., 2013; Hartenstein et al., 2015).
Type II neuroblast of the brain whose neuronal lineage enters the neuropil in a posterior medial location at the level of protocerebral bridge glomeruli 1-3 (Viktorin et al., 2011; Andrade et al., 2019).
Type II neuroblast of the brain whose neuronal lineage enters the neuropil in a posterior medial location at the level of protocerebral bridge glomeruli 4-5 (Viktorin et al., 2011; Andrade et al., 2019).
Type II neuroblast of the brain whose neuronal lineage enters the neuropil in a posterior medial location at the level of protocerebral bridge glomeruli 6-7 (Viktorin et al., 2011; Andrade et al., 2019).
A type II centromedial neuroblast of the posterior deutocerebrum. This neuroblast produces a mixed glial/neuronal progeny, although it gives rise to only a few glial cells (Viktorin et al., 2011). Its neuronal lineage enters the neuropil at the level of protocerebral bridge glomeruli 8-9 (Andrade et al., 2019).
A type II centromedial neuroblast of the posterior deutocerebrum.
A type II neuroblast that produces mostly neurons and rarely glial cells (Viktorin et al., 2011).
Neuroblast located in the dorsolateral aspect of the protocerebrum (Pereanu and Hartenstein, 2006).
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. Eckstein et al. (2020) - doi:10.1101/2020.06.12.148775 map lateral and medial hemilineages of LHl2 to lateral and medial hemilineages of DPLal2.
. Eckstein et al. (2020) - doi:10.1101/2020.06.12.148775 map dorsal and ventral hemilineages of SLPal2 to dorsal and ventral hemilineages of DPLal3.
. VLPd2 listed as equivalent to DPLam in Hartenstein et al. (2017) - FBrf0234128, but DPLam mapped to VLPd1 in Eckstein et al. (2020) - doi:10.1101/2020.06.12.148775, with no mapping for VLPd2.
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. CLp1 mapped to DPLc2/4 in Eckstein et al. (2020) - doi:10.1101/2020.06.12.148775.
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. CLp1 mapped to DPLc2/4 in Eckstein et al. (2020) - doi:10.1101/2020.06.12.148775.
. The existence of this neuroblast is inferred from lineage data (Pereanu and Hartenstein, 2006). This paper studies secondary neuroblast divisions. Although all of these lineages will correspond to a lineage from a known primary neuroblast lineage, only some will correspond to lineages from the secondary neuroblast division.
. The existence of this neuroblast is inferred from lineage data (Pereanu and Hartenstein, 2006). This paper studies secondary neuroblast divisions. Although all of these lineages will correspond to a lineage from a known primary neuroblast lineage, only some will correspond to lineages from the secondary neuroblast division.
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. Eckstein et al. (2020) - doi:10.1101/2020.06.12.148775 map anterior and posterior hemilineages of VLPd&p1 to anterior and posterior hemilineages of DPLl2.
. Eckstein et al. (2020) map anterior and posterior hemilineages of SLPad1 to anterior and posterior hemilineages of DPLl3.
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. Eckstein et al. (2020) - doi:10.1101/2020.06.12.148775 map the dorsal hemilineage of LHd2 to the dorsal hemilineage of DPLm2.
. Eckstein et al. (2020) - doi:10.1101/2020.06.12.148775 map lateral and medial hemilineages of LHp2 to lateral and medial hemilineages of DPLp1.
. Eckstein et al. (2020) - doi:10.1101/2020.06.12.148775 map the posterior hemilineage of SLPp&v1 to the posterior hemilineage of DPLp2.
Posteriormost DPL neuroblast (Pereanu and Hartenstein, 2006; Wong et al., 2013). Cell bodies of its descendants move from a postero-dorsal position in the larva to a postero-ventral position in the adult (Lovick et al., 2013). Eckstein et al. (2020) - doi:10.1101/2020.06.12.148775 map dorsal and ventral hemilineages of VLPp&l1 to dorsal and ventral hemilineages of DPLpv.
Neuroblast located in the dorsoposterior medial protocerebrum (Pereanu and Hartenstein, 2006).
. PSp3 mapped to DPMl1/2 in Eckstein et al. (2020) - doi:10.1101/2020.06.12.148775, to DPMl1 in Hartenstein et al. (2017) - FBrf0234128.
. PSp3 mapped to DPMl1/2 in Eckstein et al. (2020) - doi:10.1101/2020.06.12.148775, to DPMl1 in Hartenstein et al. (2017) - FBrf0234128.
. The existence of this neuroblast is inferred from lineage data (Pereanu and Hartenstein, 2006). This paper studies secondary neuroblast divisions. Although all of these lineages will correspond to a lineage from a known primary neuroblast lineage, only some will correspond to lineages from the secondary neuroblast division.
. The existence of this neuroblast is inferred from lineage data (Pereanu and Hartenstein, 2006). This paper studies secondary neuroblast divisions. Although all of these lineages will correspond to a lineage from a known primary neuroblast lineage, only some will correspond to lineages from the secondary neuroblast division.
. The existence of this neuroblast is inferred from lineage data (Pereanu and Hartenstein, 2006). This paper studies secondary neuroblast divisions. Although all of these lineages will correspond to a lineage from a known primary neuroblast lineage, only some will correspond to lineages from the secondary neuroblast division.
. The existence of this neuroblast is inferred from lineage data (Pereanu and Hartenstein, 2006). This paper studies secondary neuroblast divisions. Although all of these lineages will correspond to a lineage from a known primary neuroblast lineage, only some will correspond to lineages from the secondary neuroblast division.
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. The existence of this neuroblast is inferred from lineage data (Pereanu and Hartenstein, 2006). This paper studies secondary neuroblast divisions. Although all of these lineages will correspond to a lineage from a known primary neuroblast lineage, only some will correspond to lineages from the secondary neuroblast division.
. The existence of this neuroblast is inferred from lineage data (Pereanu and Hartenstein, 2006). This paper studies secondary neuroblast divisions. Although all of these lineages will correspond to a lineage from a known primary neuroblast lineage, only some will correspond to lineages from the secondary neuroblast division.
. Bridi et al. (2019) - FlyBase:FBrf0243005 suggest that Ppd5 corresponds to EBa1/p1 and DALv2/3.
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Unlike the other neuroblasts, the glial precursor (GP) does not divide to make GMCs or neurons. Dividing roughly symmetrically during embryonic stage 11, it produces two cells that migrate medially, then eventually divide to generate six longitudinal glia.
[neuroblast GPa]
[neuroblast GPb]
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. BLVa2 mapped to LHa3 in Bates et al. (2020) - FlyBase:FBrf0246460 and Eckstein et al. (2020) - doi:10.1101/2020.06.12.148775, but BLVa2 was mapped to LHa4 in Hartenstein et al. (2017) - FBrf0234128 and no updated LHa4 mapping in 2020 papers.
. Suggested to be equivalent to neuroblast BLVa2 in Hartenstein et al. (2017) - FBrf0234128, but BLVa2 mapped to LHa3 in Bates et al. (2020) - FBrf0246460 and Eckstein et al. (2020) - doi:10.1101/2020.06.12.148775 and Schlegel et al. (2023) - doi:10.1101/2023.06.27.546055. Schlegel et al. (2023) suggest that the LHa4 clone might be LHa2 with shifted cell bodies (can happen for lateral lineages).
. Eckstein et al. (2020) - doi:10.1101/2020.06.12.148775 map the dorsal hemilineage of LHd2 to the dorsal hemilineage of DPLm2.
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. The existence of this neuroblast is inferred from lineage data (Pereanu and Hartenstein, 2006). This paper studies secondary neuroblast divisions. Although all of these lineages will correspond to a lineage from a known primary neuroblast lineage, only some will correspond to lineages from the secondary neuroblast division.
Mushroom body neuroblast whose secondary lineage forms a relatively dorsal medial part of the calyx (Ito et al., 2013).
Mushroom body neuroblast whose secondary lineage forms a relatively ventral medial part of the calyx (Ito et al., 2013).
Mushroom body neuroblast whose secondary lineage forms a relatively ventral lateral part of the calyx (Ito et al., 2013).
Mushroom body neuroblast whose secondary lineage forms a relatively dorsal lateral part of the calyx (Ito et al., 2013).
An unpaired neuroblast delaminating in stage 4 along the ventral midline of the CNS. During embryonic development, it gives rise to a cluster of around 8 cells (interneurons and motorneurons) with short bilateral projections in the anterior and posterior commissures and long fibers that enter the intersegmental nerve. In the larva, this neuroblast is reactivated in segments S3 to A1. The neurons that develop from this neuroblast after larval hatching form postembryonic lineage 0.
Midline precursor cell that divides only once to produce the intersegmental interneurons dMP2 and vMP2 neurons. Despite its name, it forms bilaterally as part of the medial column of stage1 neuroblasts (Schmid et al., 1999). Appears to be three of these cells in each mandibular hemineuromere (Urbach et al., 2016) - FBrf0232096.
Neuroblast NB1-1 delaminates at stage 1 and generates the aCC and pCC neurons, glia, interneurons and additional motorneurons in the thoracic segments. In the larva, it resumes proliferation in all thoracic segments. The neurons that develop from this neuroblast after larval hatching form postembryonic lineage 16. Originally referred to as NB2-2 by Doe (1992), this was renamed to NB1-1 by Broadus et al. (1995) to reflect the fact that it makes the aCC/pCC lineage in both Drosophila and Schistocerca.
Any neuroblast NB1-1 (FBbt:00001371) that is part of some abdominal segment (FBbt:00000021).
[thoracic neuroblast; is part of; thoracic segment; neuroblast NB1-1 of thorax]
Neuroblast NB1-2 delaminates at S2 and generates 4-6 intersegmental interneurons. It also produces approximately 20 local interneurons and, in the thoracic segments, the semaphorin II (FBgn0011260) positive DC motorneuron. In the third instar larva, the lineage originated by this neuroblast is located at the ventro-lateral border of the T1-A1 neuromere. The neurons that develop from this neuroblast after larval hatching form postembryonic lineage 1, and show segment-specific differences. Originally referred to as NB1-1 by Doe (1992), this was renamed to NB1-2 by Broadus et al. (1995) to reflect the fact that it is the only engrailed-expressing anterior row neuroblast in both Drosophila and Schistocerca.
Neuroblast located at the embryonic segment border close to the tracheal pit that produces only glial cells (Schmidt et al., 1997, Schmid et al., 1999).
Neuroblast NB2-1 delaminates at S4 and generates approximately 9-15 local interneurons by embryonic stage 17. The fibers from these cells cross the midline via a single projection in a posterior fascicle of the anterior commissure. In the third instar larva, the lineage originated by this neuroblast is located near the midline on the anterior margin of the neuromere. The neurons that develop from this neuroblast after larval hatching form postembryonic lineage 2.
Neuroblast NB2-2 delaminates at S2 and generates two to three motorneurons that innervate anterior lateral muscles via the SNa. It generates a large number of local interneurons and a smaller number of late-developing intersegmental interneurons. In the larva, it resumes proliferation in all thoracic segments. The neurons that develop from this neuroblast after larval hatching form postembryonic lineage 10. Originally referred to as NB2-3 by Doe (1992), this was renamed to NB2-2 by Broadus et al. (1995) to keep the names of row 2 neuroblasts consistent with their position in Schistocerca.
Any neuroblast NB2-2 (FBbt:00001385) that is part of some abdominal segment (FBbt:00000021).
Any neuroblast NB2-2 (FBbt:00001385) that is part of some thoracic segment (FBbt:00000016).
Neuroblast NB2-3 delaminates at S5. It generates three large, round axonless cells at the dorsal side of the thoracic clones which are proposed by Schmid et al., (1999) to be latent leg motorneurons that will extend axons during leg disk eversion. It also generates 2-4 small interneurons at the ventral side of the clone. In the abdominal segments only a single large neuroblast is observed at embryonic stage 17, which either does not divide or all progeny die. This neuroblast resumes proliferation in the larva and generates postembryonic lineage 15 (Lacin and Truman, 2016). Originally referred to as NB1-2 by Doe (1992), this was renamed to NB2-3 by Broadus et al. (1995) to keep the names of row 2 neuroblasts consistent with their position in Schistocerca. Birkholz et al. (2015) suggest that NB2-3 does not generate a postembryonic lineage and NB3-2 generates postembryonic lineage 15, but Lacin and Truman (2016) provide lineage tracing and marker data showing that NB2-3 generates lineage 15.
Neuroblast NB2-4 delaminates at S4 and generates a contralaterally projecting motorneuron and approximately 8 local interneurons. This neuroblast resumes proliferation in the larva and generates postembryonic lineage 18 (Lacin and Truman, 2016). Birkholz et al. (2015) suggest that NB2-4 generates postembryonic lineage 8 and NB3-4 generates postembryonic lineage 18, but Lacin and Truman (2016) provide lineage tracing and marker data showing that NB2-4 generates lineage 18.
Any neuroblast NB2-4 (FBbt:00001411) that is part of some abdominal segment (FBbt:00000021).
[thoracic neuroblast; is part of; thoracic segment; neuroblast NB2-4 of thorax]
Neuroblast NB2-5 delaminates at S1 and generates a diverse array of cell types including motorneurons, intersegmental interneurons, local interneurons, glial cells and sometimes a PNS sub-clone. In the larva, it resumes proliferation in T1 to A1 segments. The neurons that develop from this neuroblast after larval hatching form postembryonic lineage 17.
Neuroblast NB3-1 delaminates at S3 in the medial column of neuroblasts. It generates the well characterized RP1 (FBbt:00001452), RP3 (FBbt:00001455), RP4 (FBbt:00001456) and RP5 (FBbt:00001457) motorneurons and a cluster of intersegmental interneurons. It also generates a variable number of local interneurons. In the third instar larva, the lineage originated by this neuroblast is located near the midline and corresponds to postembryonic lineage 4.
Any neuroblast NB3-1 (FBbt:00001394) that is part of some abdominal segment (FBbt:00000021).
[thoracic neuroblast; is part of; neuroblast NB3-1 of thorax; thoracic segment]
Neuroblast NB3-2 delaminates at S1 and generates as many as 6 motorneurons and a cluster of local interneurons. It is the mirror image of the clone derived from NB4-2. This neuroblast resumes proliferation in the larva and generates postembryonic lineage 7 (Lacin and Truman, 2016). Birkholz et al. (2015) suggest that NB3-2 generates postembryonic lineage 15 and NB4-2 generates postembryonic lineage 7, but Lacin and Truman (2016) provide lineage tracing and marker data showing that NB3-2 generates lineage 7.
Neuroblast NB3-3 delaminates predominantly at S4 (Schmidt et al., 1997). It generates a single motorneuron positioned midway along the dorsoventral axis, though slightly lateral and posterior. It also generates 10-18 interneurons that project across the anterior commissure (Schmid et al., 1999). In the third instar larva, the lineage originated by this neuroblast is located at the ventro-lateral anterior half of the neuromere. This neuroblast resumes proliferation in the larva and generates postembryonic lineage 8 (Lacin and Truman, 2016). Birkholz et al. (2015) suggest that NB3-3 generates postembryonic lineage 13 and NB2-4 generates postembryonic lineage 8, but Lacin and Truman (2016) provide lineage tracing and marker data showing that NB3-3 generates lineage 8.
Neuroblast NB3-4 delaminates at S5. It produces a single motorneuron located on the posterior boundary of the clone and projects into the anterior root of the ISN by embryonic stage 15. Along with several local interneurons, it also produces at least 2 intersegmental interneurons by embryonic stage 17, one extending ipsilaterally, the other crossing the anterior commissure before extending anteriorly. This neuroblast resumes proliferation in the larva and generates postembryonic lineage 25 (Lacin and Truman, 2016). Birkholz et al. (2015) suggest that NB3-4 generates postembryonic lineage 18, but Lacin and Truman (2016) identify lineage 25 and provide lineage tracing data showing that it is generated by NB3-4.
Neuroblast NB3-5 delaminates at stage 1 in the interior-most row of the lateral column (Hartenstein and Campos-Ortega, 1984), and generates a diverse array of cell types including motorneurons, intersegmental interneurons, local interneurons, glial cells and sometimes a PNS sub-clone. In the larva, it resumes proliferation in all thoracic segments, and posteriorly to A8. The neurons that develop from this neuroblast after larval hatching form postembryonic lineage 9. This is equivalent to the ‘dorsolateral neuroblast’ of Truman and Bate (1988), due to existence in A2-7 and large size of lineage (Truman and Bate, 1988 (FBrf0047815); Truman et al., 2004 (FBrf0180161); Lacin and Truman, 2016 (FBrf0231327)).
Any neuroblast NB3-5 (FBbt:00001375) that is part of some abdominal segment (FBbt:00000021).
Neuroblast NB4-1 delaminates at S3 in the medial column. It produces the putative motorneuron of the transverse nerve (FBbt:00001996) and a variety of intersegmental and local interneurons. In the third instar larva, the lineage originated by this neuroblast is located anteriorly in the medial region of the hemineuromere. In the larva, it resumes proliferation in all thoracic segments. The neurons that develop from this neuroblast after larval hatching form postembryonic lineage 14.
Neuroblast NB4-2 delaminates at S2 in the intermediate column and produces the well characterized RP2 motorneuron (FBbt:00001453), which innervates muscles 2, 9 and 11. It also produces the Cousins if RP2 motorneurons (CoR), which generate the entirety of the SNc, innervating muscles 26, 27 and 29. It also generates local interneurons and, in a small number of cases, an epidermal subclone. This neuroblast resumes proliferation in the larva and generates postembryonic lineage 13 (Lacin and Truman, 2016). Birkholz et al. (2015) suggest that NB4-2 generates postembryonic lineage 7 and NB3-3 generates postembryonic lineage 13, but Lacin and Truman (2016) provide lineage tracing and marker data showing that NB4-2 generates lineage 13.
Neuroblast NB4-3 delaminates at S5. It generates 2-3 neurosecretory cells that project together out of the CNS, appearing to join the transverse nerve in the periphery. In addition, 10-12 small, axonless interneurons are also produced at stage 17. In the larva, it resumes proliferation in all thoracic segments. The neurons that develop from this neuroblast after larval hatching form postembryonic lineage 21. Schmidt et al., (1997) describe this lineage as producing motorneurons that project into the SN. Contrarily, Schmid et al., (1999) suggest that the cells identified as motorneurons by Schmidt are actually neurosecretory cells of the TN.
Neuroblast NB4-4 delaminates at S4. It generates a single motorneuron located at the posterior ventral boundary of the clone and projects into the anterior root of the ISN by stage 5. Amongst several local interneurons, it generates at least two intersegmental interneurons, one extending anterior ipsilaterally and the other crossing the anterior commissure. In the larva, it resumes proliferation in all thoracic segments. The neurons that develop from this neuroblast after larval hatching form postembryonic lineage 24, composed exclusively of motorneurons.
Neuroblast NB5-1 delaminates at S5 in the medial column. It generates approximately 6-9 local interneurons that predominantly project across the posterior commissure (Schmid et al., 1999). This neuroblast does not resume proliferation in the larva. Schmid et al., (1999) comment that NB5-2 may give rise to a larger number of clones, including at least one motorneuron, but were not observed due to observational restrictions.
Neuroblast NB5-2 delaminates at stage 1 in the medial column (Hartenstein and Campos-Ortega, 1984). It generates a single motorneuron innervating muscle 12 via the SNb and a large number of intersegmental and local interneurons. Most of the posterior commissure derives from NB5-2 interneurons. In the third instar larva, the lineage originated by this neuroblast is located in the medial region. It resumes proliferation in segments S3 to A1, to give rise to the postembryonic lineage 6. This is equivalent to the ‘ventromedial neuroblast’ of Truman and Bate (1988), due to existence in A2-7 and its relatively medial location (Truman and Bate, 1988 (FBrf0047815); Lacin and Truman, 2016 (FBrf0231327)).
Any neuroblast NB5-2 (FBbt:00001376) that is part of some abdominal segment (FBbt:00000021).
Neuroblast NB5-3 delaminates at S1. It generates an SNa motorneuron anteriorly and intersegmental interneurons in every segment. In the larva, it resumes proliferation in S3, all thoracic segments, A1 and A7. The neurons that develop from this neuroblast after larval hatching form postembryonic lineage 5. This is equivalent to the ‘ventrolateral neuroblast’ of Truman and Bate (1988), due to existence in A2-7 and its relatively lateral location (Truman and Bate, 1988 (FBrf0047815); Lacin and Truman, 2016 (FBrf0231327)).
Any neuroblast NB5-3 (FBbt:00001390) that is part of some abdominal segment (FBbt:00000021).
Neuroblast NB5-4 most frequently delaminates at S4 in an intermediate column. In the third instar larva, the lineage originated by this neuroblast is located at the ventro-lateral region of the neuromere. Using DiI with antibody labelling, Schmidt et al., (1997) propose NB5-4 produces 5-9 thoracic neurons or 3-4 abdominal motorneurons with ipsilateral targets. Schmid et al., (1999), also use DiI with en-GFP, but find 2-3 large cells that match descriptions of CCAP/CAP+ neurosecretory cells, along with abdomen-specific interneurons. Also, Schmid et al., (1999) state that NB5-4 delaminates during S5, whilst Schmidt et al., (1997) find that delamination occurs over the period of S3/4 to S5, most frequently at S4, and as such we have chosen to define NB5-4 as a stage 4 neuroblast. According to Lacin and Truman (2016), this neuroblast resumes proliferation in the larva and generates postembryonic lineage 22. However, according to Birkholz et al. (2015) it generates lineage 20 or 22.
Any neuroblast NB5-4 (FBbt:00001416) that is part of some abdominal segment (FBbt:00000021).
[neuroblast NB5-4 of thorax; is part of; thoracic segment; thoracic neuroblast]
Neuroblast NB5-5 delaminates at S5. Thoracic and abdominal clones contain 8-11 large neurons including interneurons and neurosecretory cells. This neuroblast does not resume proliferation in the larva. Schmid et al., (1999) suggest that NB5-5 may be equivalent to clone Y described by Schmidt et al., (1997).
Neuroblast NB5-6 generates lateral sub-perineural glial cells and interneurons. This neuroblast dies by apoptosis at embryonic stage 16.
Neuroblast NB5-6 of the abdomen that delaminates at stage 1 in the lateral column. It generates 3 to 5 interneurons and 2 to 6 glial cells.
Neuroblast NB5-6 of the thorax that delaminates at late stage 8 in the lateral column. It generates 10 to 14 interneurons and 3 to 5 glial cells. It exits the cell cycle at stage 15 and dies via apoptosis at stage 16.
Neuroblast NB5-7 is located medial to NB5-4 in the embryo. It does not generate any embryonic progeny. It proliferates in the larval stages in the thoracic segments to generate postembryonic lineage 20. It is thought to have arisen as a duplication of NB5-4. Birkholz et al. (2015) suggest that NB5-4 generates postembryonic lineage 20; Lacin and Truman (2016) identify neuroblast NB5-7 and provide lineage tracing data showing that it generates lineage 20.
Neuroblast NB6-1 generates intersegmental and ~10-16 interneurons in every segment, but only generates a motorneuron in segment T1. In the larva, it resumes proliferation in segments S3 to A1, displaying segment-specific differences. The lineage originated by this neuroblast is located lateral to the median lineage, and corresponds to lineage 12.
Neuroblast NB6-2 delaminates in S2 in the intermediate column. Its lineage contains 8-16 interneurons that project in two bundles across the posterior commissure. In the larva, it resumes proliferation in segments S3 to A2 (Lacin and Truman, 2016). The neurons that develop from this neuroblast after larval hatching form postembryonic lineage 19, located at the most dorsolateral location.
Neuroblast NB6-4 generates glia in abdominal segments as well as interneurons in thoracic segments. According to Lacin and Truman (2016), this neuroblast does not resume proliferation in the larva. However, according to Birkholz et al. (2015) it generates lineage 11.
Any neuroblast NB6-4 (FBbt:00001399) that is part of some abdominal segment (FBbt:00000021).
Any neuroblast NB6-4 (FBbt:00001399) that is part of some thoracic segment (FBbt:00000016).
[neuroblast NB6-4a; neuroblast NB6-4 of abdomen]
[neuroblast NB6-4b; neuroblast NB6-4 of abdomen]
Neuroblast NB7-1 is the largest neuroblast lineage generating 40 cells or more, including the U neurons and a large number of local interneurons. It also frequently generates the putative segment boundary cells. In the larva, it resumes proliferation in segments S3 to A1. The neurons that develop from this neuroblast after larval hatching form postembryonic lineage 3, located at the posterior border of the neuromere.
Neuroblast NB7-2 delaminates at S2 in the intermediate column. Its lineage contains 8-14 interneurons that project either contralaterally in the posterior commissure or ipsilaterally. It is the only neuroblast clone that generates ipsilaterally-projecting intersegmental neurons. This neuroblast resumes proliferation in the larva and generates postembryonic lineage 11 (Lacin and Truman, 2016). Birkholz et al. (2015) suggest that NB7-2 does not generate a postembryonic lineage and NB6-4 generates postembryonic lineage 11, but Lacin and Truman (2016) provide lineage tracing and marker data showing that NB7-2 generates lineage 11.
Neuroblast NB7-3 delaminates at S5. It generates the relatively small GW motorneuron, positioned on the lateral side of the clone and projects out the posterior root of the ISN. It also generates three slightly larger interneurons that project across the posterior commissure, and a small axonless cell. It may also generate a glial cell. This neuron dies after producing the third GMC.
Neuroblast NB7-4 generates a large number of glia. In the larva, it resumes proliferation in segments S3 to A1. The neurons that develop from this neuroblast after larval hatching form postembryonic lineage 23, located dorsolaterally at the posterior border of the hemineuromere, ventral to neuropil.
Neuroblast that generates cells of the ventral nervous system, including interneurons, motor neurons and/or glial cells (Bossing et al., 1996). These neuroblasts derive from the ventral neurectoderm (Bossing et al., 1996). Applies to neuroblasts at all stages of development [FBC:CP].
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. BLAvm1 anterior hemilineage mapped to SLPa&l1 anterior hemilineage in Eckstein et al. (2020) - doi:10.1101/2020.06.12.148775, but SLPa&l1 lateral mapped to BLAl lateral.
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. SLPav1 lateral hemilineage mapped to BLAl lateral hemilineage in Eckstein et al. (2020) - doi:10.1101/2020.06.12.148775, but SLPa&l1 lateral also mapped to BLAl lateral.
. Eckstein et al. (2020) - doi:10.1101/2020.06.12.148775 map the dorsal hemilineage of SLPav2 to the dorsal hemilineage of BLD2.
. Mapped to ‘BLVa2a’ in Eckstein et al (2020) - doi:10.1101/2020.06.12.148775, but BLVa2a not mentioned elsewhere.
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. Eckstein et al. (2020) - doi:10.1101/2020.06.12.148775 map the posterior hemilineage of SLPp&v1 to the posterior hemilineage of DPLp2.
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. ‘SLPpl3 lateral’ mapped to ’new lateral’ in Bates et al. (2020) - FlyBase:FBrf0246460. SLPpl3 lateral and medial hemilineages stated to be unnamed in Hartenstein nomenclature in Eckstein et al. (2020) - doi:10.1101/2020.06.12.148775
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Neuroblast of the brain that generates a sexually-dimorphic lineage with prominent proximal neurite elaboration in the superior medial protocerebrum (Yu et al., 2013).
Any neuroblast SMPad1 (FBbt:00049463) that is part of some female organism (FBbt:00007011).
Any neuroblast SMPad1 (FBbt:00049463) that is part of some male organism (FBbt:00007004).
. SMPad2 mapped to DAMd2/3 in Eckstein et al. (2020) - doi:10.1101/2020.06.12.148775.
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Tritocerebral neuroblast that medioventrally borders the anterior deutocerebrum. Urbach et al. (2016) - FBrf0232096 state that there are 13 tritocerebral neuroblasts (Td and Tv designations), meaning that these terms are redundant with terms under ‘dorsal tritocerebral neuroblast’ and ‘ventral tritocerebral neuroblast’.
. The existence of this neuroblast is inferred from lineage data (Pereanu and Hartenstein, 2006). This paper studies secondary neuroblast divisions. Although all of these lineages will correspond to a lineage from a known primary neuroblast lineage, only some will correspond to lineages from the secondary neuroblast division.
Neuroblast of the tritocerebrum that generates two secondary hemilineages (Kuert et al., 2014; Hartenstein et al., 2018). The existence of this neuroblast is inferred from lineage data (Pereanu and Hartenstein, 2006). This paper studies secondary neuroblast divisions. Although all of these lineages will correspond to a lineage from a known primary neuroblast lineage, only some will correspond to lineages from the secondary neuroblast division.
Neuroblast of the tritocerebrum that generates a secondary lineage (Kuert et al., 2014). The existence of this neuroblast is inferred from lineage data (Pereanu and Hartenstein, 2006). This paper studies secondary neuroblast divisions. Although all of these lineages will correspond to a lineage from a known primary neuroblast lineage, only some will correspond to lineages from the secondary neuroblast division.
. The existence of this neuroblast is inferred from lineage data (Pereanu and Hartenstein, 2006). This paper studies secondary neuroblast divisions. Although all of these lineages will correspond to a lineage from a known primary neuroblast lineage, only some will correspond to lineages from the secondary neuroblast division.
. The existence of this neuroblast is inferred from lineage data (Pereanu and Hartenstein, 2006). This paper studies secondary neuroblast divisions. Although all of these lineages will correspond to a lineage from a known primary neuroblast lineage, only some will correspond to lineages from the secondary neuroblast division.