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HIC1与SWI/SNF复合物的一个特定亚基ARID1A/BAF250A相互作用。

HIC1 interacts with a specific subunit of SWI/SNF complexes, ARID1A/BAF250A.

作者信息

Van Rechem Capucine, Boulay Gaylor, Leprince Dominique

机构信息

CNRS UMR 8161, Institut de Biologie de LILLE, Université de Lille Nord de FRANCE, Institut PASTEUR de LILLE, IFR 142, 1 Rue Calmette, 59017 LILLE Cedex, France.

出版信息

Biochem Biophys Res Commun. 2009 Aug 7;385(4):586-90. doi: 10.1016/j.bbrc.2009.05.115. Epub 2009 May 30.

Abstract

HIC1, a tumor suppressor gene epigenetically silenced in many human cancers encodes a transcriptional repressor involved in regulatory loops modulating p53-dependent and E2F1-dependent cell survival and stress responses. HIC1 is also implicated in growth control since it recruits BRG1, one of the two alternative ATPases (BRM or BRG1) of SWI/SNF chromatin-remodeling complexes to repress transcription of E2F1 in quiescent fibroblasts. Here, through yeast two-hybrid screening, we identify ARID1A/BAF250A, as a new HIC1 partner. ARID1A/BAF250A is one of the two mutually exclusive ARID1-containing subunits of SWI/SNF complexes which define subsets of complexes endowed with anti-proliferative properties. Co-immunoprecipitation assays in WI38 fibroblasts and in BRG1-/- SW13 cells showed that endogenous HIC1 and ARID1A proteins interact in a BRG1-dependent manner. Furthermore, we demonstrate that HIC1 does not interact with BRM. Finally, sequential chromatin immunoprecipitation (ChIP-reChIP) experiments demonstrated that HIC1 represses E2F1 through the recruitment of anti-proliferative SWI/SNF complexes containing ARID1A.

摘要

HIC1是一种在许多人类癌症中发生表观遗传沉默的肿瘤抑制基因,它编码一种转录抑制因子,参与调节p53依赖和E2F1依赖的细胞存活及应激反应的调控环路。HIC1还与生长控制有关,因为它能招募BRG1(SWI/SNF染色质重塑复合物的两种替代ATP酶之一,另一种是BRM),从而在静止的成纤维细胞中抑制E2F1的转录。在此,通过酵母双杂交筛选,我们鉴定出ARID1A/BAF250A是一种新的HIC1相互作用蛋白。ARID1A/BAF250A是SWI/SNF复合物中两个相互排斥的含ARID1亚基之一,这些复合物具有抗增殖特性。在WI38成纤维细胞和BRG1基因敲除的SW13细胞中进行的免疫共沉淀实验表明,内源性HIC1和ARID1A蛋白以BRG1依赖的方式相互作用。此外,我们证明HIC1不与BRM相互作用。最后,连续染色质免疫沉淀(ChIP-reChIP)实验表明,HIC1通过招募含有ARID1A的抗增殖SWI/SNF复合物来抑制E2F1。

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