Global analysis of yeast mRNPs

被引:264
作者
Mitchell, Sarah F. [1 ,2 ]
Jain, Saumya [1 ,3 ]
She, Meipei [2 ,3 ]
Parker, Roy [1 ,2 ]
机构
[1] Univ Colorado, Dept Chem & Biochem, Boulder, CO 80309 USA
[2] Univ Colorado, Howard Hughes Med Inst, Boulder, CO 80309 USA
[3] Univ Arizona, Dept Mol & Cellular Biol, Tucson, AZ 85721 USA
基金
美国国家卫生研究院;
关键词
TRANSFER-RNA SYNTHETASE; TANDEM MASS-SPECTROMETRY; MESSENGER-RNA; SACCHAROMYCES-CEREVISIAE; TRANSLATIONAL CONTROL; STRESS GRANULES; PROCESSING BODIES; BINDING PROTEIN; P-BODIES; COMPLEX;
D O I
10.1038/nsmb.2468
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
Proteins regulate gene expression by controlling mRNA biogenesis, localization, translation and decay. Identifying the composition, diversity and function of mRNA-protein complexes (mRNPs) is essential to understanding these processes. In a global survey of Saccharomyces cerevisiae mRNA-binding proteins, we identified 120 proteins that cross-link to mRNA, including 66 new mRNA-binding proteins. These include kinases, RNA-modification enzymes, metabolic enzymes and tRNA-and rRNA-metabolism factors. These proteins show dynamic subcellular localization during stress, including assembly into stress granules and processing bodies (P bodies). Cross-linking and immunoprecipitation (CLIP) analyses of the P-body components Pat1, Lsm1, Dhh1 and Sbp1 identified sites of interaction on specific mRNAs, revealing positional binding preferences and co-assembly preferences. When taken together, this work defines the major yeast mRNP proteins, reveals widespread changes in their subcellular location during stress and begins to define assembly rules for P-body mRNPs.
引用
收藏
页码:127 / U161
页数:9
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