Global analysis of yeast mRNPs

被引:267
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
相关论文
共 43 条
[1]  
Andon NL, 2002, PROTEOMICS, V2, P1156, DOI 10.1002/1615-9861(200209)2:9<1156::AID-PROT1156>3.0.CO
[2]  
2-4
[3]   DREME: motif discovery in transcription factor ChIP-seq data [J].
Bailey, Timothy L. .
BIOINFORMATICS, 2011, 27 (12) :1653-1659
[4]   The mRNA-Bound Proteome and Its Global Occupancy Profile on Protein-Coding Transcripts [J].
Baltz, Alexander G. ;
Munschauer, Mathias ;
Schwanhaeusser, Bjoern ;
Vasile, Alexandra ;
Murakawa, Yasuhiro ;
Schueler, Markus ;
Youngs, Noah ;
Penfold-Brown, Duncan ;
Drew, Kevin ;
Milek, Miha ;
Wyler, Emanuel ;
Bonneau, Richard ;
Selbach, Matthias ;
Dieterich, Christoph ;
Landthaler, Markus .
MOLECULAR CELL, 2012, 46 (05) :674-690
[5]   P bodies promote stress granule assembly in Saccharomyces cerevisiae [J].
Buchan, J. Ross ;
Muhlrad, Denise ;
Parker, Roy .
JOURNAL OF CELL BIOLOGY, 2008, 183 (03) :441-455
[6]   Stress-specific composition, assembly and kinetics of stress granules in Saccharomyces cerevisiae [J].
Buchan, J. Ross ;
Yoon, Je-Hyun ;
Parker, Roy .
JOURNAL OF CELL SCIENCE, 2011, 124 (02) :228-239
[7]   Eukaryotic Stress Granules: The Ins and Outs of Translation [J].
Buchan, J. Ross ;
Parker, Roy .
MOLECULAR CELL, 2009, 36 (06) :932-941
[8]   Insights into RNA Biology from an Atlas of Mammalian mRNA-Binding Proteins [J].
Castello, Alfredo ;
Fischer, Bernd ;
Eichelbaum, Katrin ;
Horos, Rastislav ;
Beckmann, Benedikt M. ;
Strein, Claudia ;
Davey, Norman E. ;
Humphreys, David T. ;
Preiss, Thomas ;
Steinmetz, Lars M. ;
Krijgsveld, Jeroen ;
Hentze, Matthias W. .
CELL, 2012, 149 (06) :1393-1406
[9]   The decapping activator Lsm1p-7p-Pat1p complex has the intrinsic ability to distinguish between oligoadenylated and polyadenylated RNAs [J].
Chowdhury, Ashis ;
Mukhopadhyay, Jaba ;
Tharun, Sundaresan .
RNA, 2007, 13 (07) :998-1016
[10]   Eukaryotic mRNA decapping [J].
Coller, J ;
Parker, R .
ANNUAL REVIEW OF BIOCHEMISTRY, 2004, 73 :861-890