RNA polymerase II elongation factors use conserved regulatory mechanisms

被引:2
|
作者
Chen, Ying [1 ,2 ]
Cramer, Patrick [1 ]
机构
[1] Max Planck Inst Multidisciplinary Sci, Dept Mol Biol, Fassberg 11, D-37077 Gottingen, Germany
[2] Shandong Univ, Dept Clin Lab, Qilu Hosp, Jinan 250012, Shandong, Peoples R China
关键词
TRANSCRIPTION FACTORS TFIIF; STRUCTURAL BASIS; HIV-1; TAT; COMPLEX; ELONGIN; ELL; INTEGRATOR; SUBUNIT; ACTIVATION; PROTEIN;
D O I
10.1016/j.sbi.2023.102766
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
RNA polymerase II (Pol II) transcription is regulated by many elongation factors. Among these factors, TFIIF, PAF-RTF1, ELL and Elongin stimulate mRNA chain elongation by Pol II. Cryo-EM structures of Pol II complexes with these elongation factors now reveal some general principles on how elongation factors bind Pol II and how they stimulate transcription. All four elongation factors contact Pol II at domains external 2 and protrusion, whereas TFIIF and ELL additionally bind the Pol II lobe. All factors apparently stabilize cleft-flanking elements, whereas RTF1 and Elongin additionally approach the active site with a latch element and may influence catalysis or translocation. Due to the shared binding sites on Pol II, factor binding is mutually exclusive, and thus it remains to be studied what determines which elongation factors bind at a certain gene and under which condition.
引用
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页数:9
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