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SENP1介导的Gli1去SUMO化作用减弱了音猬因子信号通路。

DeSUMOylation of Gli1 by SENP1 Attenuates Sonic Hedgehog Signaling.

作者信息

Liu Huaize, Yan Sen, Ding Jie, Yu Ting-Ting, Cheng Steven Y

机构信息

Department of Developmental Genetics, School of Basic Medical Sciences, Nanjing Medical University, Nanjing, Jiangsu, China.

Department of Developmental Genetics, School of Basic Medical Sciences, Nanjing Medical University, Nanjing, Jiangsu, China

出版信息

Mol Cell Biol. 2017 Aug 28;37(18). doi: 10.1128/MCB.00579-16. Print 2017 Sep 15.

Abstract

The transcriptional output of the Sonic Hedgehog morphogenic pathway is orchestrated by three Krüppel family transcription factors, Gli1 to -3, which undergo extensive posttranslational modifications, including ubiquitination and SUMOylation. Here, we report that the sentrin-specific peptidase SENP1 is the specific deSUMOylation enzyme for Gli1. We show that SUMOylation stabilizes Gli1 by competing with ubiquitination at conserved lysine residues and that SUMOylated Gli1 is enriched in the nucleus, suggesting that SUMOylation is a nuclear localization signal for Gli1. Finally, we show that small interfering RNA (siRNA)-mediated knockdown of SENP1 augments the ability of Shh to sustain the proliferation of cerebellar granule cell precursors, demonstrating the physiological significance of the negative regulation of Shh signaling by SENP1.

摘要

音猬因子(Sonic Hedgehog)形态发生通路的转录输出由三个克鲁ppel家族转录因子Gli1至Gli3精心调控,这些转录因子会经历广泛的翻译后修饰,包括泛素化和小泛素样修饰(SUMOylation)。在此,我们报告泛素样修饰特异性蛋白酶1(SENP1)是Gli1的特异性去SUMOylation酶。我们表明,SUMOylation通过在保守赖氨酸残基处与泛素化竞争来稳定Gli1,并且SUMO化的Gli1在细胞核中富集,这表明SUMOylation是Gli1的核定位信号。最后,我们表明,通过小干扰RNA(siRNA)介导的SENP1敲低增强了音猬因子(Shh)维持小脑颗粒细胞前体增殖的能力,证明了SENP1对Shh信号负调控的生理意义。

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