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The super elongation complex (SEC) and MLL in development and disease.超级延伸复合物(SEC)和 MLL 在发育和疾病中的作用。
Genes Dev. 2011 Apr 1;25(7):661-72. doi: 10.1101/gad.2015411.
2
Pausing of RNA polymerase II disrupts DNA-specified nucleosome organization to enable precise gene regulation.RNA 聚合酶 II 的暂停会破坏 DNA 特异性核小体的组织,从而实现精确的基因调控。
Cell. 2010 Nov 12;143(4):540-51. doi: 10.1016/j.cell.2010.10.004.
3
Controlling cellular P-TEFb activity by the HIV-1 transcriptional transactivator Tat.通过 HIV-1 转录反式激活蛋白 Tat 控制细胞 P-TEFb 的活性。
PLoS Pathog. 2010 Oct 14;6(10):e1001152. doi: 10.1371/journal.ppat.1001152.
4
CDK12 is a transcription elongation-associated CTD kinase, the metazoan ortholog of yeast Ctk1.CDK12 是一种转录延伸相关的 CTD 激酶,是酵母 Ctk1 的后生动物直系同源物。
Genes Dev. 2010 Oct 15;24(20):2303-16. doi: 10.1101/gad.1968210.
5
Nuclear organization and dynamics of 7SK RNA in regulating gene expression.7SK RNA 的核组织和动力学在调节基因表达中的作用。
Mol Biol Cell. 2010 Dec;21(23):4184-96. doi: 10.1091/mbc.E10-02-0105. Epub 2010 Sep 29.
6
The mechanism of release of P-TEFb and HEXIM1 from the 7SK snRNP by viral and cellular activators includes a conformational change in 7SK.病毒和细胞激活物将 P-TEFb 和 HEXIM1 从 7SK snRNP 中释放出来的机制包括 7SK 的构象变化。
PLoS One. 2010 Aug 23;5(8):e12335. doi: 10.1371/journal.pone.0012335.
7
Transcription elongation takes central stage: the P-TEFb connection.转录延伸成为核心:P-TEFb的联系。
Cell Cycle. 2010 Aug 1;9(15):2933-4. doi: 10.4161/cc.9.15.12698.
8
HEXIM1 targets a repeated GAUC motif in the riboregulator of transcription 7SK and promotes base pair rearrangements.HEXIM1 靶向转录 7SK 核糖调控因子中的重复 GAUC 基序,并促进碱基对重排。
Nucleic Acids Res. 2010 Nov;38(21):7749-63. doi: 10.1093/nar/gkq660. Epub 2010 Jul 31.
9
RNA-mediated displacement of an inhibitory snRNP complex activates transcription elongation.RNA 介导的抑制性 snRNP 复合物的置换激活转录延伸。
Nat Struct Mol Biol. 2010 Jul;17(7):815-21. doi: 10.1038/nsmb.1827. Epub 2010 Jun 20.
10
Crystal structure of HIV-1 Tat complexed with human P-TEFb.HIV-1 Tat 与人 P-TEFb 复合物的晶体结构
Nature. 2010 Jun 10;465(7299):747-51. doi: 10.1038/nature09131.

7SK snRNA:一种在调控真核转录中起主要作用的非编码 RNA。

7SK snRNA: a noncoding RNA that plays a major role in regulating eukaryotic transcription.

机构信息

Department of Medicine, Rosalind Russel Medical Research Center, University of California, San Francisco, CA, USA.

出版信息

Wiley Interdiscip Rev RNA. 2012 Jan-Feb;3(1):92-103. doi: 10.1002/wrna.106. Epub 2011 Aug 18.

DOI:10.1002/wrna.106
PMID:21853533
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3223291/
Abstract

The human 7SK small nuclear RNA (snRNA) is an abundant noncoding RNA whose function has been conserved in evolution from invertebrates to humans. It is transcribed by RNA polymerase III (RNAPIII) and is located in the nucleus. Together with associated cellular proteins, 7SK snRNA regulates the activity of the positive transcription elongation factor b (P-TEFb). In humans, this regulation is accomplished by the recruitment of P-TEFb by the 7SK snRNA-binding proteins, hexamethylene bisacetamide (HMBA)-induced mRNA 1/2 (HEXIM1 or HEXIM2), which inhibit the kinase activity of P-TEFb. P-TEFb regulates the transition of promoter proximally paused RNA polymerase II (RNAPII) into productive elongation, thereby, allowing efficient mRNA production. The protein composition of the 7SK small nuclear ribonucleoprotein (snRNP) is regulated dynamically. While the Lupus antigen (La)-related protein 7 (LARP7) is a constitutive component, the methylphosphate capping enzyme (MePCE) associates secondarily to phosphorylate the 5' end of 7SK snRNA. The release of active P-TEFb is closely followed by release of HEXIM proteins and both are replaced by heterogeneous nuclear ribonucleoproteins (hnRNPs). The released P-TEFb activates the expression of most cellular and viral genes. Regulated release of P-TEFb determines the expression pattern of many of the genes that respond to environmental stimuli and regulate growth, proliferation, and differentiation of cells.

摘要

人类 7SK 小核 RNA(snRNA)是一种丰富的非编码 RNA,其功能在从无脊椎动物到人类的进化过程中得到了保守。它由 RNA 聚合酶 III(RNAPIII)转录,位于细胞核内。7SK snRNA 与相关的细胞蛋白一起,调节正转录延伸因子 b(P-TEFb)的活性。在人类中,这种调节是通过 7SK snRNA 结合蛋白六亚甲基双乙酰胺(HMBA)诱导的 mRNA 1/2(HEXIM1 或 HEXIM2)募集 P-TEFb 来实现的,它们抑制 P-TEFb 的激酶活性。P-TEFb 调节启动子附近暂停的 RNA 聚合酶 II(RNAPII)向生产性延伸的转变,从而允许有效的 mRNA 产生。7SK 小核核糖核蛋白(snRNP)的蛋白质组成是动态调节的。虽然狼疮抗原(La)相关蛋白 7(LARP7)是一个组成性成分,但甲基磷酸封端酶(MePCE)则作为次要成分与磷酸化 7SK snRNA 的 5' 端结合。活性 P-TEFb 的释放紧随其后是 HEXIM 蛋白的释放,两者都被异质核核糖核蛋白(hnRNPs)取代。释放的 P-TEFb 激活大多数细胞和病毒基因的表达。P-TEFb 的调节释放决定了许多对环境刺激做出反应并调节细胞生长、增殖和分化的基因的表达模式。