| Literature DB >> 29588524 |
Fang Yu1, Guang Shi1,2, Shimeng Cheng1, Jiwei Chen1, Shwu-Yuan Wu3, Zhiqiang Wang1, Nansong Xia4, Yunhao Zhai1, Zhenxing Wang1, Yu Peng1, Dong Wang1, James X Du1, Lujian Liao1, Sheng-Zhong Duan5, Tieliu Shi1, Jinke Cheng4, Cheng-Ming Chiang3, Jiwen Li6, Jiemin Wong7.
Abstract
Regulation of transcription is fundamental to the control of cellular gene expression and function. Although recent studies have revealed a role for the oncoprotein MYC in amplifying global transcription, little is known as to how the global transcription is suppressed. Here we report that SUMO and MYC mediate opposite effects upon global transcription by controlling the level of CDK9 sumoylation. On one hand, SUMO suppresses global transcription via sumoylation of CDK9, the catalytic subunit of P-TEFb kinase essential for productive transcriptional elongation. On the other hand, MYC amplifies global transcription by antagonizing CDK9 sumoylation. Sumoylation of CDK9 blocks its interaction with Cyclin T1 and thus the formation of active P-TEFb complex. Transcription profiling analyses reveal that SUMO represses global transcription, particularly of moderately to highly expressed genes and by generating a sumoylation-resistant CDK9 mutant, we confirm that sumoylation of CDK9 inhibits global transcription. Together, our data reveal that SUMO and MYC oppositely control global gene expression by regulating the dynamic sumoylation and desumoylation of CDK9.Entities:
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Year: 2018 PMID: 29588524 PMCID: PMC5993822 DOI: 10.1038/s41422-018-0023-9
Source DB: PubMed Journal: Cell Res ISSN: 1001-0602 Impact factor: 25.617