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本文引用的文献

1
When ubiquitin meets ubiquitin receptors: a signalling connection.当泛素遇上泛素受体:一种信号连接
Nat Rev Mol Cell Biol. 2003 Jun;4(6):491-7. doi: 10.1038/nrm1124.
2
How the ubiquitin-proteasome system controls transcription.泛素-蛋白酶体系统如何控制转录。
Nat Rev Mol Cell Biol. 2003 Mar;4(3):192-201. doi: 10.1038/nrm1049.
3
Bre1, an E3 ubiquitin ligase required for recruitment and substrate selection of Rad6 at a promoter.Bre1,一种在启动子处招募Rad6并进行底物选择所必需的E3泛素连接酶。
Mol Cell. 2003 Jan;11(1):267-74. doi: 10.1016/s1097-2765(02)00802-x.
4
A conserved RING finger protein required for histone H2B monoubiquitination and cell size control.一种组蛋白H2B单泛素化和细胞大小控制所需的保守环状结构域蛋白。
Mol Cell. 2003 Jan;11(1):261-6. doi: 10.1016/s1097-2765(02)00826-2.
5
Activation of the E3 ligase function of the BRCA1/BARD1 complex by polyubiquitin chains.多聚泛素链对BRCA1/BARD1复合物E3连接酶功能的激活作用。
EMBO J. 2002 Dec 16;21(24):6755-62. doi: 10.1093/emboj/cdf691.
6
NIRF, a novel RING finger protein, is involved in cell-cycle regulation.NIRF是一种新型的环指蛋白,参与细胞周期调控。
Biochem Biophys Res Commun. 2002 Aug 23;296(3):530-6. doi: 10.1016/s0006-291x(02)00890-2.
7
Gene silencing: trans-histone regulatory pathway in chromatin.基因沉默:染色质中的组蛋白间调控途径
Nature. 2002 Aug 1;418(6897):498. doi: 10.1038/nature00970. Epub 2002 Jul 14.
8
Targeted disruption of Np95 gene renders murine embryonic stem cells hypersensitive to DNA damaging agents and DNA replication blocks.Np95基因的靶向破坏使小鼠胚胎干细胞对DNA损伤剂和DNA复制阻滞高度敏感。
J Biol Chem. 2002 Sep 13;277(37):34549-55. doi: 10.1074/jbc.M205189200. Epub 2002 Jun 25.
9
Ubiquitination of histone H2B regulates H3 methylation and gene silencing in yeast.组蛋白H2B的泛素化调控酵母中的H3甲基化及基因沉默。
Nature. 2002 Jul 4;418(6893):104-8. doi: 10.1038/nature00883. Epub 2002 Jun 23.
10
Methylation of histone H3 by COMPASS requires ubiquitination of histone H2B by Rad6.COMPASS介导的组蛋白H3甲基化需要Rad6介导的组蛋白H2B泛素化。
J Biol Chem. 2002 Aug 9;277(32):28368-71. doi: 10.1074/jbc.C200348200. Epub 2002 Jun 17.

Np95是一种具有泛素连接酶活性的组蛋白结合蛋白。

Np95 is a histone-binding protein endowed with ubiquitin ligase activity.

作者信息

Citterio Elisabetta, Papait Roberto, Nicassio Francesco, Vecchi Manuela, Gomiero Paola, Mantovani Roberto, Di Fiore Pier Paolo, Bonapace Ian Marc

机构信息

Istituto FIRC di Oncologia Molecolare, 20139 Milan, Italy.

出版信息

Mol Cell Biol. 2004 Mar;24(6):2526-35. doi: 10.1128/MCB.24.6.2526-2535.2004.

DOI:10.1128/MCB.24.6.2526-2535.2004
PMID:14993289
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC355858/
Abstract

Np95 is an important determinant in cell cycle progression. Its expression is tightly regulated and becomes detectable shortly before the entry of cells into S phase. Accordingly, Np95 is absolutely required for the G1/S transition. Its continued expression throughout the S/G2/M phases further suggests additional roles. Indeed, Np95 has been implicated in DNA damage response. Here, we show that Np95 is tightly bound to chromatin in vivo and that it binds to histones in vivo and in vitro. The binding to histones is direct and shows a remarkable preference for histone H3 and its N-terminal tail. A novel protein domain, the SRA-YDG domain, contained in Np95 is indispensable both for the interaction with histones and for chromatin binding in vivo. Np95 contains a RING finger. We show that this domain confers E3 ubiquitin ligase activity on Np95, which is specific for core histones, in vitro. Finally, Np95 shows specific E3 activity for histone H3 when the endogenous core octamer, coimmunoprecipitating with Np95, is used as a substrate. Histone ubiquitination is an important determinant in the regulation of chromatin structure and gene transcription. Thus, the demonstration that Np95 is a chromatin-associated ubiquitin ligase suggests possible molecular mechanisms for its action as a cell cycle regulator.

摘要

Np95是细胞周期进程中的一个重要决定因素。其表达受到严格调控,在细胞进入S期前不久可检测到。因此,G1/S期转换绝对需要Np95。它在整个S/G2/M期持续表达,这进一步表明它还有其他作用。事实上,Np95已被证明与DNA损伤反应有关。在这里,我们表明Np95在体内与染色质紧密结合,并且在体内和体外都能与组蛋白结合。与组蛋白的结合是直接的,并且对组蛋白H3及其N端尾巴表现出显著的偏好。Np95中包含的一个新的蛋白质结构域,即SRA-YDG结构域,对于与组蛋白的相互作用以及在体内与染色质的结合都是不可或缺的。Np95含有一个环状结构域。我们表明,该结构域赋予Np95体外E3泛素连接酶活性,该活性对核心组蛋白具有特异性。最后,当与Np95共免疫沉淀的内源性核心八聚体用作底物时,Np95对组蛋白H3表现出特异性E3活性。组蛋白泛素化是染色质结构和基因转录调控中的一个重要决定因素。因此,Np95是一种与染色质相关的泛素连接酶这一证明,为其作为细胞周期调节因子的作用提供了可能 的分子机制。