CDK9 and PP2A regulate RNA polymerase II transcription termination and coupled RNA maturation

被引:15
|
作者
Tellier, Michael [1 ]
Zaborowska, Justyna [1 ]
Neve, Jonathan [2 ]
Nojima, Takayuki [3 ]
Hester, Svenja [2 ]
Fournier, Marjorie [2 ]
Furger, Andre [2 ]
Murphy, Shona [1 ]
机构
[1] Univ Oxford, Sir William Dunn Sch Pathol, Oxford, England
[2] Univ Oxford, Dept Biochem, Oxford, England
[3] Kyushu Univ, Med Inst Bioregulat, Fukuoka, Japan
基金
英国生物技术与生命科学研究理事会; 英国惠康基金;
关键词
CDK9; mRNA cleavage and polyadenylation complex; PP2A; RNA polymerase II; transcription; PRE-MESSENGER-RNA; POL-II; ALTERNATIVE CLEAVAGE; SENSITIVE KINASE; POLYADENYLATION; CTD; DOMAIN; PHOSPHORYLATION; PHOSPHATASES; INHIBITORS;
D O I
10.15252/embr.202154520
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
CDK9 is a kinase critical for the productive transcription of protein-coding genes by RNA polymerase II (pol II). As part of P-TEFb, CDK9 phosphorylates the carboxyl-terminal domain (CTD) of pol II and elongation factors, which allows pol II to elongate past the early elongation checkpoint (EEC) encountered soon after initiation. We show that, in addition to halting pol II at the EEC, loss of CDK9 activity causes premature termination of transcription across the last exon, loss of polyadenylation factors from chromatin, and loss of polyadenylation of nascent transcripts. Inhibition of the phosphatase PP2A abrogates the premature termination and loss of polyadenylation caused by CDK9 inhibition, indicating that this kinase/phosphatase pair regulates transcription elongation and RNA processing at the end of protein-coding genes. We also confirm the splicing factor SF3B1 as a target of CDK9 and show that SF3B1 in complex with polyadenylation factors is lost from chromatin after CDK9 inhibition. These results emphasize the important roles that CDK9 plays in coupling transcription elongation and termination to RNA maturation downstream of the EEC.
引用
收藏
页数:22
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