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TFⅡH参与调控RNA聚合酶Ⅱ介导的mRNA转录的研究进展 被引量:2

Advances in studies of TFⅡH in the regulation of RNA polymerase Ⅱ mediated mRNA transcription
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摘要 通用转录因子TFⅡH(transcription factorⅡH)在RNA聚合酶Ⅱ(RNA PolⅡ)介导mRNA的转录中起着非常重要的作用,且主要是通过磷酸化RNA PolⅡ大亚基的羧基末端结构域(CTD)的各个位点来调控转录过程。转录启动前,TFⅡH及其他转录因子与RNA PolⅡ结合形成转录起始前复合物(preinitiation complex,PIC),而后TFⅡH的亚基CAK通过磷酸化RNAPⅡCTD的第五位丝氨酸(Ser5)和第七位丝氨酸(Ser7)促进转录的起动。而CAK磷酸化Ser5的同时也能够促使另一个激酶CDK9磷酸化RNAPⅡCTD的第二位丝氨酸(Ser2),该过程参与调控转录的延伸以及终止。 TF Ⅱ H (transcription factor Ⅱ H) plays an essential role in the mRNA transcription mediated by RNA polymerase [[ (RNA Pol Ⅱ ) and mainly regulated by the phosphorylation of several sites of RNA Pol Ⅱ C-terminal domain (CTD). Before the initiation of transcription,TF Ⅱ H and other transcriptional factors integrate with RNA Pol Ⅱ and then form a preinitiation complex (PIC). The initiation of transcription is promoted by RNA Pol Ⅱ CTD Serine-5 and Ser- ine-7 which are phosphorylated by TF Ⅱ H subunit CAK. The phosphorylation of Serine-5 by CAK also triggeres the other kinase CDK9 to phosphorylate RNA Pol Ⅱ CTD Serine-2. Further- ly,the phosphorylation of RNA Pol Ⅱ CTD Serine-2 participats in the extension and termination of mRNA transcription.
出处 《南昌大学学报(医学版)》 CAS 2013年第7期72-75,共4页 Journal of Nanchang University:Medical Sciences
基金 国家自然科学基金(81160196 30660010)
关键词 TFⅡH CDK7 MAT1 MRNA 转录 TFⅡ H CDK7 MAT1 mRNA transcription
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  • 1Fesquet D,Labb J C,Derancourt J ,et al. The MO15 gene en- codes the catalytic subunit of a protein kinase that activatescde2 and other cyclin-dependent kinases (CDKs) through phosphorylation of Thr161 and its homologues[J]. EMBO J, 1993,12 : 3111-3121.
  • 2Larochelle S, Batliner J, Gamble M J, et al. Dichotomous but stringent substrate selection by the dual-function Cdk7 com- plex revealed by chemical genetics[J]. Nat Struct Mol Biol, 2006,13 : 55-62.
  • 3Busso D,Keriel A,Sandrock B,et al. Distinct regions of MAT1 regulate cdk7 kinase and TF lI H transcription activities[J]. J Biol Chem, 2000,275 : 22815-22823.
  • 4Tremeau Bravard A,Perez C,Egly J M. A role of the C-termi- nal part of p44 in the promoter escape activity of transcription factor I1 H[J]. J Biol Chem, 2001,276 : 27693-27697.
  • 5Coin F,Oksenych V,Egly J M. Distinct roles for the XPB/p52 and XPD/p44 subcomplexes of TF lI H in damaged DNA open- ing during nucleotide excision repair [ J ]. Mol Cell, 2007,26: 245-256.
  • 6Pearson A,Greenblatt J. Modular organization of the E2F1 ac- tivation domain and its interaction with general transcription factors TBP and TF 1I H[J]. Oncogene, 1997,15 : 2643-2658.
  • 7Xiao H, Pearson A, Coulombe B, et al. Binding of basal tran- scription factor TF H H to the acidic activation domains of VP16 and p53[J]. Mol Cell Biol, 1994,14 : 7013-7024.
  • 8Ranish J A, Hahn S, Lu Y, et al. Identification of TFB5, a new component of general transcription and DNA repair factor l] H[J]. Nat Genet,2004,36:707-713.
  • 9Akhtar M S, Heidemann M, Tietjen J R, et al. TF II H kinase places bivalent marks on the carboxy-terminal domain of RNA polymerase 1] [J]. Mol Ce11,2009,34:387-393.
  • 10Egloff S, O' Reilly D, Chapman R D, et al. Serine-7 of the RNA polymerase [I CTD is specifically required for snRNA gene expression[J]. Science,2007,318:1777-1779.

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