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C-Jun招募NSL复合物,通过调节H4K16乙酰化和促进抑制性NuRD复合物的释放来调控其靶基因表达。

C-Jun recruits the NSL complex to regulate its target gene expression by modulating H4K16 acetylation and promoting the release of the repressive NuRD complex.

作者信息

Liu Yan, Long Yuehong, Xing Zhaobin, Zhang Daoyong

机构信息

College of Life Sciences, Hebei United University, Tangshan, China.

Department of Biochemistry and Molecular Biology, The Pennsylvania State University, University Park, PA, USA.

出版信息

Oncotarget. 2015 Jun 10;6(16):14497-506. doi: 10.18632/oncotarget.3988.

Abstract

The proto-oncogene c-Jun plays essential roles in various cellular processes, including cell proliferation, cell differentiation, and cellular apoptosis. Enormous efforts have been made to understand the mechanisms regulating c-Jun activation. The males absent on the first (MOF)-containing non-specific lethal (NSL) complex has been shown to positively regulate gene expression. However, the biological function of the NSL complex is largely unknown. Here we present evidence showing that c-Jun recruits the NSL complex to c-Jun target genes upon activation. The NSL complex catalyzes H4K16 acetylation at c-Jun target genes, thereby promoting c-Jun target gene transcription. More interestingly, we also found that the NSL complex promotes the release of the repressive NuRD complex from c-Jun target genes, thus activating c-Jun. Our findings not only reveal a new mechanism regulating c-Jun activation, but also identify the NSL complex as a c-Jun co-activator in c-Jun-regulated gene expression, expanding our knowledge of the function of the NSL complex in gene expression regulation.

摘要

原癌基因c-Jun在多种细胞过程中发挥着重要作用,包括细胞增殖、细胞分化和细胞凋亡。人们为了解调节c-Jun激活的机制付出了巨大努力。已证明含雄性第一缺失(MOF)的非特异性致死(NSL)复合物能正向调节基因表达。然而,NSL复合物的生物学功能在很大程度上尚不清楚。在此,我们提供证据表明,c-Jun在激活后会将NSL复合物招募至c-Jun靶基因。NSL复合物在c-Jun靶基因上催化H4K16乙酰化,从而促进c-Jun靶基因转录。更有趣的是,我们还发现NSL复合物促进抑制性核小体重塑与去乙酰化酶(NuRD)复合物从c-Jun靶基因上释放,从而激活c-Jun。我们的发现不仅揭示了一种调节c-Jun激活的新机制,还确定NSL复合物是c-Jun调节基因表达中的一种c-Jun共激活因子,扩展了我们对NSL复合物在基因表达调控中功能的认识。

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