Cdk9 regulates a promoter-proximal checkpoint to modulate RNA polymerase II elongation rate in fission yeast

被引:58
作者
Booth, Gregory T. [1 ]
Parua, Pabitra K. [2 ]
Sanso, Miriam [2 ]
Fisher, Robert P. [2 ]
Lis, John T. [1 ]
机构
[1] Cornell Univ, Dept Mol Biol & Genet, 107 Biotechnol Bldg,526 Campus Rd, Ithaca, NY 14853 USA
[2] Icahn Sch Med Mt Sinai, Dept Oncol Sci, New York, NY 10029 USA
关键词
CARBOXY-TERMINAL DOMAIN; TRANSCRIPTION ELONGATION; P-TEFB; CAPPING ENZYME; SENSITIVE ALLELES; BUR1; KINASE; SPT5; COMPLEX; TFIIH; PHOSPHORYLATION;
D O I
10.1038/s41467-018-03006-4
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Post-translational modifications of the transcription elongation complex provide mechanisms to fine-tune gene expression, yet their specific impacts on RNA polymerase II regulation remain difficult to ascertain. Here, in Schizosaccharomyces pombe, we examine the role of Cdk9, and related Mcs6/Cdk7 and Lsk1/Cdk12 kinases, on transcription at base-pair resolution with Precision Run-On sequencing (PRO-seq). Within a minute of Cdk9 inhibition, phosphorylation of Pol II-associated factor, Spt5 is undetectable. The effects of Cdk9 inhibition are more severe than inhibition of Cdk7 and Cdk12, resulting in a shift of Pol II toward the transcription start site (TSS). A time course of Cdk9 inhibition reveals that early transcribing Pol II can escape promoter-proximal regions, but with a severely reduced elongation rate of only similar to 400 bp/min. Our results in fission yeast suggest the existence of a conserved global regulatory checkpoint that requires Cdk9 kinase activity.
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页数:10
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