Insights into RNA Biology from an Atlas of Mammalian mRNA-Binding Proteins

被引:1621
作者
Castello, Alfredo [1 ]
Fischer, Bernd [1 ]
Eichelbaum, Katrin [1 ]
Horos, Rastislav [1 ]
Beckmann, Benedikt M. [1 ]
Strein, Claudia [1 ]
Davey, Norman E. [1 ]
Humphreys, David T. [2 ]
Preiss, Thomas [2 ,3 ]
Steinmetz, Lars M. [1 ]
Krijgsveld, Jeroen [1 ]
Hentze, Matthias W. [1 ,2 ]
机构
[1] EMBL, D-69117 Heidelberg, Germany
[2] Victor Chang Cardiac Res Inst, Div Mol Genet, Sydney, NSW 2010, Australia
[3] Australian Natl Univ, John Curtin Sch Med Res, Genome Biol Dept, Canberra, ACT 0200, Australia
基金
澳大利亚研究理事会; 英国医学研究理事会;
关键词
NUCLEIC-ACIDS; CROSS-LINKING; IRE-BP; CYCLOPHILIN; DEHYDROGENASE; EXPRESSION; IDENTIFICATION; INTERACTS; ACONITASE; DISORDER;
D O I
10.1016/j.cell.2012.04.031
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-binding proteins (RBPs) determine RNA fate from synthesis to decay. Employing two complementary protocols for covalent UV crosslinking of RBPs to RNA, we describe a systematic, unbiased, and comprehensive approach, termed "interactome capture,'' to define the mRNA interactome of proliferating human HeLa cells. We identify 860 proteins that qualify as RBPs by biochemical and statistical criteria, adding more than 300 RBPs to those previously known and shedding light on RBPs in disease, RNA-binding enzymes of intermediary metabolism, RNA-binding kinases, and RNA-binding architectures. Unexpectedly, we find that many proteins of the HeLa mRNA interactome are highly intrinsically disordered and enriched in short repetitive amino acid motifs. Interactome capture is broadly applicable to study mRNA interactome composition and dynamics in varied biological settings.
引用
收藏
页码:1393 / 1406
页数:14
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