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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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