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通过抑制 p53 乙酰化和转录因子 Sp1 结合来调节细胞周期蛋白依赖性激酶抑制剂 1A 基因(CDKN1A)的表达。

Regulation of the cyclin-dependent kinase inhibitor 1A gene (CDKN1A) by the repressor BOZF1 through inhibition of p53 acetylation and transcription factor Sp1 binding.

机构信息

Department of Biochemistry and Molecular Biology, Brain Korea 21 Project for Medical Science, Severance Biomedical Research Institute, Yonsei University School of Medicine, 134 ShinChon-Dong, SeoDaeMoon-Ku, Seoul 120-752, Korea.

出版信息

J Biol Chem. 2013 Mar 8;288(10):7053-64. doi: 10.1074/jbc.M112.416297. Epub 2013 Jan 17.

DOI:10.1074/jbc.M112.416297
PMID:23329847
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3591615/
Abstract

The human POZ domain and Krüppel-like zinc finger (POK) family proteins play important roles in the regulation of apoptosis, cell proliferation, differentiation, development, oncogenesis, and tumor suppression. A novel POK family transcription factor, BTB/POZ and zinc finger domains factor on chromosome 1 (BOZF-1; also called ZBTB8A), contains a POZ domain and two C2H2-type Krüppel-like zinc fingers and is localized at nuclear speckles. Compared with paired normal tissues, BOZF1 expression is increased in cancer tissues of the prostate, breast, and cervix. BOZF1 repressed the transcription of p21WAF/CDKN1A by acting on the proximal promoter concentrated with Sp1-binding GC boxes. BOZF1 competed with Sp1 in binding to GC boxes 1-5/6 of the CDKN1A proximal promoter. In addition, BOZF1 interacted with p53 and decreased the acetylation of p53 by p300, which reduced the DNA binding activity of p53 at the far distal p53-binding element. BOZF1 blocked the two major molecular events that are important in both constitutive and inducible transcription activation of CDKN1A. BOZF1 is unique in that it bound to all the proximal GC boxes to repress transcription, and it inhibited p53 acetylation without affecting p53 stability. BOZF1 might be a novel proto-oncoprotein that stimulates cell proliferation.

摘要

人类 POZ 结构域和 Krüppel 样锌指(POK)家族蛋白在调控细胞凋亡、细胞增殖、分化、发育、致癌和肿瘤抑制中发挥重要作用。一种新型的 POK 家族转录因子,1 号染色体上的 BTB/POZ 和锌指结构域因子(BOZF-1;也称为 ZBTB8A),含有一个 POZ 结构域和两个 C2H2 型 Krüppel 样锌指,并定位于核斑点。与配对的正常组织相比,BOZF1 在前列腺癌、乳腺癌和宫颈癌组织中的表达增加。BOZF1 通过作用于富含 Sp1 结合 GC 盒的近端启动子来抑制 p21WAF/CDKN1A 的转录。BOZF1 与 Sp1 竞争结合 CDKN1A 近端启动子的 GC 盒 1-5/6。此外,BOZF1 与 p53 相互作用,并通过 p300 降低 p53 的乙酰化,从而降低 p53 在远位 p53 结合元件上的 DNA 结合活性。BOZF1 阻断了 CDKN1A 组成性和诱导性转录激活中两个重要的主要分子事件。BOZF1 的独特之处在于它结合了所有的近端 GC 盒来抑制转录,并且它抑制了 p53 乙酰化而不影响 p53 的稳定性。BOZF1 可能是一种新的原癌蛋白,可刺激细胞增殖。

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本文引用的文献

1
KR-POK interacts with p53 and represses its ability to activate transcription of p21WAF1/CDKN1A.KR-POK 与 p53 相互作用,抑制其激活 p21WAF1/CDKN1A 转录的能力。
Cancer Res. 2012 Mar 1;72(5):1137-48. doi: 10.1158/0008-5472.CAN-11-2433. Epub 2012 Jan 17.
2
The proto-oncoprotein KR-POK represses transcriptional activation of CDKN1A by MIZ-1 through competitive binding.原癌蛋白 KR-POK 通过竞争性结合抑制 MIZ-1 对 CDKN1A 的转录激活。
Oncogene. 2012 Mar 15;31(11):1442-58. doi: 10.1038/onc.2011.331. Epub 2011 Aug 1.
3
A novel POK family transcription factor, ZBTB5, represses transcription of p21CIP1 gene.一种新型的POK家族转录因子ZBTB5可抑制p21CIP1基因的转录。
J Biol Chem. 2009 Jul 24;284(30):19856-66. doi: 10.1074/jbc.M109.025817. Epub 2009 Jun 2.
4
ZBTB2, a novel master regulator of the p53 pathway.锌指蛋白转录因子2(ZBTB2),一种p53信号通路的新型主调控因子。
J Biol Chem. 2009 Jul 3;284(27):17935-46. doi: 10.1074/jbc.M809559200. Epub 2009 Apr 20.
5
Proto-oncogene FBI-1 represses transcription of p21CIP1 by inhibition of transcription activation by p53 and Sp1.原癌基因FBI-1通过抑制p53和Sp1的转录激活来抑制p21CIP1的转录。
J Biol Chem. 2009 May 8;284(19):12633-44. doi: 10.1074/jbc.M809794200. Epub 2009 Feb 25.
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Zbtb4 represses transcription of P21CIP1 and controls the cellular response to p53 activation.Zbtb4抑制P21CIP1的转录并控制细胞对p53激活的反应。
EMBO J. 2008 Jun 4;27(11):1563-74. doi: 10.1038/emboj.2008.85. Epub 2008 May 1.
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How important are post-translational modifications in p53 for selectivity in target-gene transcription and tumour suppression?p53的翻译后修饰对于靶基因转录选择性和肿瘤抑制有多重要?
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Functional analysis of the role of POK transcriptional repressors.POK转录抑制因子作用的功能分析
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Tip60-dependent acetylation of p53 modulates the decision between cell-cycle arrest and apoptosis.依赖Tip60的p53乙酰化作用调节细胞周期停滞与凋亡之间的抉择。
Mol Cell. 2006 Dec 28;24(6):827-39. doi: 10.1016/j.molcel.2006.11.021.
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