Acheate-scute like 1 (Ascl1) Is Required for Normal Delta-like (Dll) Gene Expression and Notch Signaling During Retinal Development

被引:72
作者
Nelson, Branden R. [1 ]
Hartman, Byron H. [1 ]
Ray, Catherine A. [1 ]
Hayashi, Toshinori [1 ]
Bermingham-McDonogh, Olivia [1 ]
Reh, Thomas A. [1 ]
机构
[1] Univ Washington, Sch Med, Dept Biol Struct, Seattle, WA 98195 USA
关键词
notch activity; delta-like; Dll1; Dll4; Dll3; Ascl1; Neurog2; Hes1; Hes5; Hes6; retinal development; mutual and lateral inhibition; molecular circuit; MAMMALIAN ACHAETE-SCUTE; LOOP-HELIX GENES; BHLH GENES; CELL FATE; CORTICAL NEUROGENESIS; NEURAL REGENERATION; PRONEURAL BHLH; GANGLION-CELLS; CHICK HOMOLOG; MULLER GLIA;
D O I
10.1002/dvdy.21848
中图分类号
R602 [外科病理学、解剖学]; R32 [人体形态学];
学科分类号
100101 ;
摘要
Delta gene expression in Drosophila is regulated by proneural basic helix-loop-helix (bHLH) transcription factors, such as acheate-scute. In vertebrates, multiple Delta-like and proneural bHLH genes are expressed during neurogenesis, especially in the retina. We recently uncovered a relationship between Acheate-scute like 1 (Ascl1), Delta-like genes, and Notch in chick retinal progenitors. Here, we report that mammalian retinal progenitors are also the primary source of Delta-like genes, likely signaling through Notch among themselves, while differentiating neurons expressed Jagged2. Ascl1 is coexpressed in Delta-like and Notch active progenitors, and required for normal Delta-like gene expression and Notch signaling. We also reveal a role for Ascl1 in the regulation of Hes6, a proneurogenic factor that inhibits Notch signaling to promote neural rather than glial differentiation. Thus, these results suggest a molecular mechanism whereby attenuated Notch levels coupled with reduced proneurogenic activity in progenitors leads to increased gliogenesis and decreased neurogenesis in the Ascl1-deficient retina. Developmental Dynamics 238:2163-2178, 2009. (C) 2009 Wiley-Liss, Inc.
引用
收藏
页码:2163 / 2178
页数:16
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