The exozyme model: A continuum of functionally distinct complexes

被引:22
作者
Kiss, Daniel L. [1 ,2 ]
Andrulis, Erik D. [1 ,2 ]
机构
[1] Case Western Reserve Univ, Sch Med, Dept Mol Biol & Microbiol, Cleveland, OH 44106 USA
[2] Case Western Reserve Univ, Sch Med, Cell Biol Program, Cleveland, OH 44106 USA
关键词
exosome; exozyme; RNA processing; RNA turnover; RNA surveillance; ribonuclease; Rrp6; Dis3; exosome subunit; MESSENGER-RNA DECAY; GENOME-WIDE ANALYSIS; PRE-RIBOSOMAL-RNA; HUMAN PM-SCL; QUALITY-CONTROL; YEAST EXOSOME; CORE EXOSOME; NUCLEAR-RNA; POLYMERASE-II; ENDONUCLEOLYTIC CLEAVAGE;
D O I
10.1261/rna.2364811
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Exosome complexes are composed of 10 to 11 subunits and are involved in multiple facets of 3' -> 5' RNA processing and turnover. The current paradigm stipulates that a uniform, stoichiometric core exosome, composed of single copies of each subunit, carries out all RNA metabolic functions in vivo. While core composition is well established in vitro, available genetic, cell biological, proteomic, and transcriptomic data raise questions about whether individual subunits contribute to RNA metabolic functions exclusively within the complex. Here, we recount the current understanding of the core exosome model and show predictions of the core model that are not satisfied by the available evidence. To resolve this discrepancy, we propose the exozyme hypothesis, a novel model stipulating that while exosome subunits can and do carry out certain functions within the core, subsets of exosome subunits and cofactors also assemble into a continuum of compositionally distinct complexes-exozymes-with different RNA specificities. The exozyme model is consistent with all published data and provides a new framework for understanding the general mechanisms and regulation of RNA processing and turnover.
引用
收藏
页码:1 / 13
页数:13
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