Notch-dependent binary fate choice regulates the Netrin pathway to control axon guidance of Drosophila visual projection neurons
Cell Reports, ISSN: 2211-1247, Vol: 42, Issue: 3, Page: 112143
2023
- 4Citations
- 8Captures
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
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Metrics Details
- Citations4
- Citation Indexes4
- CrossRef2
- Captures8
- Readers8
Article Description
Notch-dependent binary fate choice between sister neurons is one of the mechanisms to generate neural diversity. How these upstream neural fate specification programs regulate downstream effector genes to control axon targeting and neuropil assembly remains less well understood. Here, we report that Notch-dependent binary fate choice in Drosophila medulla neurons is required to regulate the Netrin axon guidance pathway, which controls targeting of transmedullary (Tm) neurons to lobula. In medulla neurons of Notch-on hemilineage composed of mostly lobula-targeting neurons, Notch signaling is required to activate the expression of Netrin-B and repress the expression of its repulsive receptor Unc-5. Turning off Unc-5 is necessary for Tm neurons to target lobula. Furthermore, Netrin-B provided by Notch-on medulla neurons is required for correct targeting of Tm axons from later-generated medulla columns. Thus, the coordinate regulation of Netrin pathway components by Notch signaling ensures correct targeting of Tm axons and contributes to the neuropil assembly.
Bibliographic Details
http://www.sciencedirect.com/science/article/pii/S2211124723001547; http://dx.doi.org/10.1016/j.celrep.2023.112143; http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85148665322&origin=inward; http://www.ncbi.nlm.nih.gov/pubmed/36821442; https://linkinghub.elsevier.com/retrieve/pii/S2211124723001547; https://dx.doi.org/10.1016/j.celrep.2023.112143
Elsevier BV
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