Regulation of POU genes by castor and hunchback establishes layered compartments in the Drosophila CNS

被引:225
作者
Kambadur, R
Koizumi, K
Stivers, C
Nagle, J
Poole, SJ
Odenwald, WF [1 ]
机构
[1] NINDS, Neurogenet Unit, Neurochem Lab, NIH, Bethesda, MD 20892 USA
[2] NINDS, DNA Sequencing Facil, NIH, Bethesda, MD 20892 USA
[3] Univ Calif Santa Barbara, Dept Mol Cellular & Dev Biol, Santa Barbara, CA 93106 USA
关键词
castor; hunchback; zinc finger proteins; CNS POU gene regulation;
D O I
10.1101/gad.12.2.246
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
POU transcription factors participate in cell-identity decisions during nervous system development, yet little is known about the regulatory networks controlling their expression, We report all known Drosophila POU genes require castor (cas) for correct CNS expression. drifter and I-POU depend on cas for full expression, whereas pdm-1 and pdm-2 are negatively regulated. cas encodes a zinc finger protein that shares DNA-binding specificity with another pdm repressor: the gap segmentation gene regulator Hunchback (Hb). Our studies reveal that the embryonic CNS contains sequentially generated neuroblast sublineages that can be distinguished by their expression of either Hb, Pdm-1, or Cas. Hb and Cas may directly silence pdm expression in early and late developing sublineages, given that pdm-1 cis-regulatory DNA contains greater than or equal to 32 Hb/Cas-binding sites and its enhancer(s) are ectopically activated in cas(-) neuroblasts. In addition, the targeted misexpression of Cas in all neuroblast lineages reduces Pdm-1 expression without altering Hb expression. By ensuring correct POU gene expression boundaries, hb and cas maintain temporal subdivisions in the cell-identity circuitry controlling CNS development.
引用
收藏
页码:246 / 260
页数:15
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