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P300转录抑制由SUMO修饰介导。

P300 transcriptional repression is mediated by SUMO modification.

作者信息

Girdwood David, Bumpass Donna, Vaughan Owen A, Thain Alison, Anderson Lisa A, Snowden Andrew W, Garcia-Wilson Elisa, Perkins Neil D, Hay Ronald T

机构信息

Institute of Biomolecular Sciences, University of Street Andrews, North Haugh, United Kingdom.

出版信息

Mol Cell. 2003 Apr;11(4):1043-54. doi: 10.1016/s1097-2765(03)00141-2.

Abstract

p300 and CREB binding protein can both activate and repress transcription. Here, we locate the CRD1 transcriptional repression domain between residues 1017 and 1029 of p300. This region contains two copies of the sequence psiKxE that are modified by the ubiquitin-like protein SUMO-1. Mutations that reduce SUMO modification increase p300-mediated transcriptional activity and expression of a SUMO-specific protease or catalytically inactive Ubc9 relieved repression, demonstrating that p300 repression was mediated by SUMO conjugation. SUMO-modified CRD1 domain bound HDAC6 in vitro, and p300 repression was relieved by histone deacetylase inhibition and siRNA-mediated ablation of HDAC6 expression. These results reveal a mechanism controlling p300 function and suggest that SUMO-dependent repression is mediated by recruitment of HDAC6.

摘要

p300和CREB结合蛋白既能激活转录,也能抑制转录。在此,我们将CRD1转录抑制结构域定位在p300的1017至1029位氨基酸残基之间。该区域包含两个psiKxE序列拷贝,它们被类泛素蛋白SUMO-1修饰。降低SUMO修饰的突变会增加p300介导的转录活性,而SUMO特异性蛋白酶或催化失活的Ubc9可缓解抑制作用,表明p300的抑制作用是由SUMO缀合介导的。SUMO修饰的CRD1结构域在体外与HDAC6结合,组蛋白去乙酰化酶抑制和siRNA介导的HDAC6表达缺失可缓解p300的抑制作用。这些结果揭示了一种控制p300功能的机制,并表明SUMO依赖性抑制是由HDAC6的募集介导的。

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