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Prevention of medulla neuron dedifferentiation by Nerfin-1 requires inhibition of Notch activity
Author(s) -
Jiajun Xu,
Hao Xue,
Meng-Xin Yin,
Yi Lu,
Yunyun Jin,
Jinjin Xu,
Ling Ge,
Wenqing Wu,
Margaret S. Ho,
Yingzi Yang,
Yun Zhao,
Lei Zhang
Publication year - 2017
Publication title -
development
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.754
H-Index - 325
eISSN - 1477-9129
pISSN - 0950-1991
DOI - 10.1242/dev.141341
Subject(s) - biology , neuroblast , notch signaling pathway , medulla , neuron , microbiology and biotechnology , neuroscience , neurogenesis , anatomy , transcription factor , central nervous system , signal transduction , genetics , gene
The Drosophila larval central nervous system comprises the central brain, ventral nerve cord and optic lobe. In these regions, neuroblasts (NBs) divide asymmetrically to self-renew and generate differentiated neurons or glia. To date, mechanisms of preventing neuron dedifferentiation are still unclear, especially in the optic lobe. Here, we show that the zinc-finger transcription factor Nerfin-1 is expressed in early-stage medulla neurons and is essential for maintaining their differentiation. Loss of Nerfin-1 activates Notch signaling, which promotes neuron-to-NB reversion. Repressing Notch signaling largely rescues dedifferentiation in nerfin-1 mutant clones. Thus, we conclude that Nerfin-1 represses Notch activity in medulla neurons and prevents them from dedifferentiation.

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