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The Ets protein pointed prevents both premature differentiation and dedifferentiation of Drosophila intermediate neural progenitors
Author(s) -
Yong-Gang Xie,
Xiaosu Li,
Xiaobing Deng,
Yanjun Hou,
Krysten O’Hara,
Andreacarola Urso,
Ying Peng,
Li Chen,
Sijun Zhu
Publication year - 2016
Publication title -
development
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.15
H-Index - 36
eISSN - 1477-9129
pISSN - 0950-1991
DOI - 10.1242/dev.137281
Subject(s) - neuroblast , biology , gene knockdown , neurogenesis , progenitor cell , progenitor , microbiology and biotechnology , mutant , neural stem cell , ectopic expression , cellular differentiation , genetics , gene , stem cell
Intermediate neural progenitors (INPs) need to avoid both dedifferentiation and differentiation during neurogenesis, but the underlying mechanisms are not well understood. In Drosophila, the Ets protein Pointed P1 (PntP1) is required to generate INPs from type II neuroblasts. Here, we investigated how PntP1 promotes INP generation. By generating pntP1-specific mutants and using RNAi knockdown, we show that the loss of PntP1 leads to both an increase in type II neuroblast number and the elimination of INPs. The elimination of INPs results from the premature differentiation of INPs due to ectopic Prospero expression in newly generated immature INPs (imINPs), whereas the increase in type II neuroblasts results from the dedifferentiation of imINPs due to loss of Earmuff at later stages of imINP development. Furthermore, reducing Buttonhead enhances the loss of INPs in pntP1 mutants, suggesting that PntP1 and Buttonhead act cooperatively to prevent premature INP differentiation. Our results demonstrate that PntP1 prevents both the premature differentiation and the dedifferentiation of INPs by regulating the expression of distinct target genes at different stages of imINP development.

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