Transcriptional elongation control in developmental gene expression, aging, and disease

被引:33
作者
Aoi, Yuki [1 ]
Shilatifard, Ali [1 ]
机构
[1] Northwestern Univ, Simpson Querrey Inst Epigenet, Feinberg Sch Med, Dept Biochem & Mol Genet, Chicago, IL 60611 USA
关键词
RNA-POLYMERASE-II; HISTONE H2B MONOUBIQUITINATION; PRE-MESSENGER-RNA; FACTORS REPRESS TRANSCRIPTION; CAP-BINDING COMPLEX; C-TERMINAL REPEAT; YEAST SKI COMPLEX; P-TEFB; PAF1; COMPLEX; POL-II;
D O I
10.1016/j.molcel.2023.10.004
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
The elongation stage of transcription by RNA polymerase II (RNA Pol II) is central to the regulation of gene expression in response to developmental and environmental cues in metazoan. Dysregulated transcriptional elongation has been associated with developmental defects as well as disease and aging processes. Decades of genetic and biochemical studies have painstakingly identified and characterized an ensemble of factors that regulate RNA Pol II elongation. This review summarizes recent findings taking advantage of genetic engineering techniques that probe functions of elongation factors in vivo. We propose a revised model of elongation control in this accelerating field by reconciling contradictory results from the earlier biochemical evidence and the recent in vivo studies. We discuss how elongation factors regulate promoter-proximal RNA PolII pause release, transcriptional elongation rate and processivity, RNA PolII stability and RNA processing, and how perturbation of these processes is associated with developmental disorders, neurodegenerative disease, cancer, and aging.
引用
收藏
页码:3972 / 3999
页数:28
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