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本文引用的文献

1
High mobility group proteins and their post-translational modifications.高迁移率族蛋白及其翻译后修饰
Biochim Biophys Acta. 2008 Sep;1784(9):1159-66. doi: 10.1016/j.bbapap.2008.04.028. Epub 2008 May 10.
2
Kinetic analysis of acetylation-dependent Pb1 bromodomain-histone interactions.乙酰化依赖性Pb1溴结构域与组蛋白相互作用的动力学分析
Biophys Chem. 2008 Jul;136(1):7-12. doi: 10.1016/j.bpc.2008.03.011. Epub 2008 Apr 4.
3
Structural insights into human KAP1 PHD finger-bromodomain and its role in gene silencing.人类KAP1植物同源结构域指状结构-溴结构域的结构解析及其在基因沉默中的作用
Nat Struct Mol Biol. 2008 Jun;15(6):626-33. doi: 10.1038/nsmb.1416. Epub 2008 May 18.
4
Structural basis of site-specific histone recognition by the bromodomains of human coactivators PCAF and CBP/p300.人共激活因子PCAF和CBP/p300的溴结构域对位点特异性组蛋白识别的结构基础
Structure. 2008 Apr;16(4):643-52. doi: 10.1016/j.str.2008.01.010.
5
BAF180 is a critical regulator of p21 induction and a tumor suppressor mutated in breast cancer.BAF180是p21诱导的关键调节因子,也是在乳腺癌中发生突变的肿瘤抑制因子。
Cancer Res. 2008 Mar 15;68(6):1667-74. doi: 10.1158/0008-5472.CAN-07-5276.
6
Thermodynamic analysis of acetylation-dependent Pb1 bromodomain-histone H3 interactions.乙酰化依赖性Pb1溴结构域与组蛋白H3相互作用的热力学分析
Anal Biochem. 2008 Mar 15;374(2):304-12. doi: 10.1016/j.ab.2007.12.008. Epub 2007 Dec 14.
7
Autoregulation of the rsc4 tandem bromodomain by gcn5 acetylation.通过Gcn5乙酰化对rsc4串联溴结构域进行自调控。
Mol Cell. 2007 Sep 7;27(5):817-28. doi: 10.1016/j.molcel.2007.08.018.
8
Nucleosome organization and targeting of SWI/SNF chromatin-remodeling complexes: contributions of the DNA sequence.核小体组织与SWI/SNF染色质重塑复合物的靶向作用:DNA序列的贡献
Biochem Cell Biol. 2007 Aug;85(4):419-25. doi: 10.1139/O07-070.
9
An essential switch in subunit composition of a chromatin remodeling complex during neural development.神经发育过程中染色质重塑复合物亚基组成的关键转变。
Neuron. 2007 Jul 19;55(2):201-15. doi: 10.1016/j.neuron.2007.06.019.
10
The HMG-box: a versatile protein domain occurring in a wide variety of DNA-binding proteins.HMG框:一种存在于多种DNA结合蛋白中的多功能蛋白结构域。
Cell Mol Life Sci. 2007 Oct;64(19-20):2590-606. doi: 10.1007/s00018-007-7162-3.

多溴蛋白-1:PBAF复合物的染色质靶向亚基。

Polybromo-1: the chromatin targeting subunit of the PBAF complex.

作者信息

Thompson Martin

机构信息

Department of Chemistry, Michigan Technological University, 1400 Townsend Drive, Houghton, MI 49931, USA.

出版信息

Biochimie. 2009 Mar;91(3):309-19. doi: 10.1016/j.biochi.2008.10.019. Epub 2008 Dec 3.

DOI:10.1016/j.biochi.2008.10.019
PMID:19084573
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2646799/
Abstract

The human Polybromo-1 protein (Pb1) was recently identified as a unique subunit of the PBAF (Polybromo, Brg1-Associated Factors) chromatin-remodeling complex required for kinetochore localization during mitosis and the transcription of estrogen-responsive genes. Pb1 coordinates key features common to all remodeling complexes, including chromatin localization, recruitment of protein subunits and alteration of chromatin architecture. A comprehensive analysis of individual domains composing Pb1 is used to propose new information regarding the function of Pb1 in the PBAF chromatin-remodeling complex. The newly identified regulatory role of this important protein is also examined to explain both native function and the emerging role of Pb1 as a tumor suppressor found to be mutated in breast cancer.

摘要

人类多溴蛋白-1(Pb1)最近被确定为PBAF(多溴、Brg1相关因子)染色质重塑复合体的一个独特亚基,该复合体在有丝分裂期间着丝粒定位和雌激素反应基因的转录过程中是必需的。Pb1协调所有重塑复合体共有的关键特征,包括染色质定位、蛋白质亚基的募集以及染色质结构的改变。对组成Pb1的各个结构域进行全面分析,以提出有关Pb1在PBAF染色质重塑复合体中功能的新信息。还研究了这种重要蛋白质新确定的调节作用,以解释其天然功能以及Pb1作为在乳腺癌中发现发生突变的肿瘤抑制因子的新出现作用。