P-TEFb: The master regulator of transcription elongation

被引:50
作者
Fujinaga, Koh [1 ]
Huang, Fang [1 ,2 ]
Peterlin, B. Matija [1 ]
机构
[1] Univ Calif San Francisco, Dept Med Microbiol & Immunol, San Francisco, CA 94143 USA
[2] Hubei Jiangxia Lab, Wuhan 430000, Peoples R China
关键词
RNA-POLYMERASE-II; HUMAN-IMMUNODEFICIENCY-VIRUS; NUCLEAR RIBONUCLEOPROTEIN SNRNP; LONG TERMINAL REPEAT; 7SK SNRNA; CDK9/CYCLIN T1; HIV-1; TAT; ACTIVATION DOMAIN; GENE-EXPRESSION; HIGH-AFFINITY;
D O I
10.1016/j.molcel.2022.12.006
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The positive transcription elongation factor b (P-TEFb) is composed of cyclins T1 or T2 and cyclin-dependent kinase 9 that regulate the elongation phase of transcription by RNA polymerase II. By antagonizing negative elongation factors and phosphorylating the C-terminal domain of RNA polymerase II, P-TEFb facilitates the elongation and co-transcriptional processing of nascent transcripts. This step is critical for the expression of most eukaryotic genes. In growing cells, P-TEFb is regulated negatively by its reversible associations with HEXIM1/2 in the 7SK snRNP and positively by a number of transcription factors, as well as the super elonga-tion complex. In resting cells, P-TEFb falls apart, and cyclin T1 is degraded by the proteasome. This complex regulation of P-TEFb has evolved for the precise temporal and spatial regulation of gene expression in the organism. Its dysregulation contributes to inflammatory and neoplastic conditions.
引用
收藏
页码:393 / 403
页数:11
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