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The Brm-HDAC3-Erm repressor complex suppresses dedifferentiation in Drosophila type II neuroblast lineages.Brm-HDAC3-Erm抑制复合物可抑制果蝇II型神经母细胞谱系中的去分化过程。
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Bre1a, a histone H2B ubiquitin ligase, regulates the cell cycle and differentiation of neural precursor cells.Bre1a,一种组蛋白 H2B 泛素连接酶,调节神经前体细胞的细胞周期和分化。
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菲斯家族转录因子:调控哺乳动物发育中的神经系统的神经发生和细胞命运

Fez family transcription factors: controlling neurogenesis and cell fate in the developing mammalian nervous system.

作者信息

Eckler Matthew J, Chen Bin

机构信息

Department of Molecular, Cell and Developmental Biology, University of California, Santa Cruz, CA, USA.

出版信息

Bioessays. 2014 Aug;36(8):788-97. doi: 10.1002/bies.201400039. Epub 2014 Jun 10.

DOI:10.1002/bies.201400039
PMID:24913420
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5472476/
Abstract

Fezf1 and Fezf2 are highly conserved transcription factors that were first identified by their specific expression in the anterior neuroepithelium of Xenopus and zebrafish embryos. These proteins share an N-terminal domain with homology to the canonical engrailed repressor motif and a C-terminal DNA binding domain containing six C2H2 zinc-finger repeats. Over a decade of study indicates that the Fez proteins play critical roles during nervous system development in species as diverse as fruit flies and mice. Herein we discuss recent progress in understanding the functions of Fezf1 and Fezf2 in neurogenesis and cell fate specification during mammalian nervous system development. Going forward we believe that efforts should focus on understanding how expression of these factors is precisely regulated, and on identifying target DNA sequences and interacting partners. Such knowledge may reveal the mechanisms by which Fezf1 and Fezf2 accomplish both independent and redundant functions across diverse tissue and cell types.

摘要

Fezf1和Fezf2是高度保守的转录因子,最初是通过它们在非洲爪蟾和斑马鱼胚胎前神经上皮中的特异性表达而被鉴定出来的。这些蛋白质共享一个与典型的engrailed阻遏基序具有同源性的N端结构域和一个包含六个C2H2锌指重复序列的C端DNA结合结构域。十多年的研究表明,Fez蛋白在果蝇和小鼠等多种物种的神经系统发育过程中发挥着关键作用。在此,我们讨论了在理解Fezf1和Fezf2在哺乳动物神经系统发育过程中的神经发生和细胞命运决定功能方面的最新进展。展望未来,我们认为研究应集中在理解这些因子的表达是如何被精确调控的,以及识别靶DNA序列和相互作用的伙伴。这些知识可能揭示Fezf1和Fezf2在不同组织和细胞类型中实现独立和冗余功能的机制。