The role of O-GlcNAcylation in RNA polymerase II transcription

被引:2
|
作者
Lewis, Brian A. [1 ]
机构
[1] NCI, Gene Regulat Sect LP, Ctr Canc Res, NIH, Bethesda, MD 20892 USA
关键词
C-TERMINAL DOMAIN; PAUSE RELEASE; MEDIATOR COMPLEX; MAMMALIAN-CELLS; LARGEST SUBUNIT; REPEAT DOMAIN; IN-VITRO; P-TEFB; PROMOTER; ELONGATION;
D O I
10.1016/j.jbc.2024.105705
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
Eukaryotic RNA polymerase II (RNAPII) is responsible for the transcription of the protein-coding genes in the cell. Enormous progress has been made in discovering the protein activities that are required for transcription to occur, but the effects of post-translational modifications (PTMs) on RNAPII transcriptional regulation are much less understood. Most of our understanding relates to the cyclin-dependent kinases (CDKs), which appear to act relatively early in transcription. However, it is becoming apparent that other PTMs play a crucial role in the transcriptional cycle, and it is doubtful that any sort of complete understanding of this regulation is attainable without understanding the spectra of PTMs that occur on the transcriptional machinery. Among these is OGlcNAcylation. Recent experiments have shown that the OGlcNAc PTM likely has a prominent role in transcription. This review will cover the role of the O-GlcNAcylation in RNAPII transcription during initiation, pausing, and elongation, which will hopefully be of interest to both O-GlcNAc and RNAPII transcription researchers.
引用
收藏
页数:9
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