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钙调蛋白驱动的核内进入:性别决定和终末分化的触发因素

Calmodulin-driven nuclear entry: trigger for sex determination and terminal differentiation.

作者信息

Hanover John A, Love Dona C, Prinz William A

机构信息

Laboratory of Cell Biochemistry and Biology, NIDDK, NIH, Bethesda, MD 20892, USA.

出版信息

J Biol Chem. 2009 May 8;284(19):12593-7. doi: 10.1074/jbc.R800076200. Epub 2009 Jan 5.

Abstract

We originally proposed that Ca(2+)-calmodulin mediates a novel nuclear entry pathway distinct from the canonic Ran-dependent pathway (Sweitzer, T. D., and Hanover, J. A. (1996) Proc. Natl. Acad. Sci. U. S. A. 93, 14574-14579). Although seemingly redundant, Ca(2+)-calmodulin-driven nuclear entry is now known to facilitate nuclear delivery of architectural transcription factors to chromatin. Intriguingly, defects in calmodulin-driven nuclear import of the transcription factors SRY and SOX9 in Sertoli cells lead to human sex reversal diseases with altered male gonad development. Calmodulin-triggered nuclear entry is an evolutionarily ancient feature of eukaryotes observed from yeast to man. Ca(2+)-calmodulin-triggered nuclear entry of key architectural transcription factors is a potentially key epigenetic regulator of terminal differentiation in response to cell signaling.

摘要

我们最初提出,钙调蛋白介导了一种不同于经典的依赖于Ran的途径的新型核进入途径(斯韦策,T.D.,和汉诺威,J.A.(1996年)《美国国家科学院院刊》93卷,第14574 - 14579页)。尽管看似多余,但现在已知钙调蛋白驱动的核进入有助于将结构转录因子核转运至染色质。有趣的是,支持细胞中转录因子SRY和SOX9的钙调蛋白驱动的核输入缺陷会导致男性性腺发育改变的人类性反转疾病。钙调蛋白触发的核进入是从酵母到人类的真核生物进化上古老的特征。关键结构转录因子的钙调蛋白触发的核进入是响应细胞信号的终末分化的潜在关键表观遗传调节因子。

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