Unravelling the Mechanisms of RNA Helicase Regulation

被引:96
作者
Sloan, Katherine E. [1 ]
Bohnsack, Markus T. [1 ,2 ]
机构
[1] Univ Med Ctr Gottingen, Dept Mol Biol, Humboldtallee 23, D-37073 Gottingen, Germany
[2] Univ Gottingen, Gottingen Ctr Mol Biosci, Justus von Liebig Weg 11, D-37077 Gottingen, Germany
关键词
G-PATCH PROTEIN; STRUCTURAL BASIS; ATPASE ACTIVITY; FUNCTIONAL-ANALYSIS; BOX ATPASE; TRI-SNRNP; RIG-I; COMPLEX; DOMAIN; PRP43;
D O I
10.1016/j.tibs.2018.02.001
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 helicases are critical regulators at the nexus of multiple pathways of RNA metabolism, and in the complex cellular environment, tight spatial and temporal regulation of their activity is essential. Dedicated protein cofactors play key roles in recruiting helicases to specific substrates and modulating their catalytic activity. Alongside individual RNA helicase cofactors, networks of cofactors containing evolutionarily conserved domains such as the G-patch and MIF4G domains highlight the potential for cross-regulation of different aspects of gene expression. Structural analyses of RNA helicase-cofactor complexes now provide insight into the diverse mechanisms by which cofactors can elicit specific and coordinated regulation of RNA helicase action. Furthermore, post-translational modifications (PTMs) and long non-coding RNA (IncRNA) regulators have recently emerged as novel modes of RNA helicase regulation.
引用
收藏
页码:237 / 250
页数:14
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