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多种转录因子对视网膜细胞命运特化的调控

Regulation of retinal cell fate specification by multiple transcription factors.

作者信息

Ohsawa Ryosuke, Kageyama Ryoichiro

机构信息

Institute for Virus Research, Kyoto University, Shogoin-Kawahara, Sakyo-ku, Kyoto 606-8507, Japan.

出版信息

Brain Res. 2008 Feb 4;1192:90-8. doi: 10.1016/j.brainres.2007.04.014. Epub 2007 Apr 11.

Abstract

Retinal cell fate specification is strictly regulated by multiple transcription factors. Regarding regulation of cell proliferation and differentiation, basic helix-loop-helix (bHLH) type repressors and activators function in an antagonistic manner. Repressor-type bHLH factors maintain retinal progenitor cells, whereas activator-type bHLH factors promote neuronal cell fate determination. However, bHLH genes alone are not sufficient for acquiring proper neuronal subtype identity. Recent findings have shown that retinal cell fate specification is regulated by combinations of bHLH and homeobox genes. It is conceivable that homeobox genes confer positional identity whereas bHLH genes regulate neuronal determination and differentiation. Moreover, it has been shown that bHLH genes implicated in retinal cell fate determination regulate expression of other bHLH genes, implying that there is a complicated transcription network regulating retinal development.

摘要

视网膜细胞命运的特化受到多种转录因子的严格调控。关于细胞增殖和分化的调控,碱性螺旋-环-螺旋(bHLH)型抑制因子和激活因子以拮抗方式发挥作用。抑制型bHLH因子维持视网膜祖细胞,而激活型bHLH因子促进神经元细胞命运的决定。然而,仅bHLH基因不足以获得适当的神经元亚型身份。最近的研究发现表明,视网膜细胞命运的特化是由bHLH基因和同源框基因的组合调控的。可以想象,同源框基因赋予位置身份,而bHLH基因调节神经元的决定和分化。此外,已经表明参与视网膜细胞命运决定的bHLH基因调节其他bHLH基因的表达,这意味着存在一个复杂的转录网络调节视网膜发育。

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