| Literature DB >> 31665645 |
Anna L Mallam1, Wisath Sae-Lee2, Jeffrey M Schaub2, Fan Tu2, Anna Battenhouse2, Yu Jin Jang3, Jonghwan Kim3, John B Wallingford2, Ilya J Finkelstein2, Edward M Marcotte4, Kevin Drew5.
Abstract
RNA-binding proteins (RBPs) play essential roles in biology and are frequently associated with human disease. Although recent studies have systematically identified individual RNA-binding proteins, their higher-order assembly into ribonucleoprotein (RNP) complexes has not been systematically investigated. Here, we describe a proteomics method for systematic identification of RNP complexes in human cells. We identify 1,428 protein complexes that associate with RNA, indicating that more than 20% of known human protein complexes contain RNA. To explore the role of RNA in the assembly of each complex, we identify complexes that dissociate, change composition, or form stable protein-only complexes in the absence of RNA. We use our method to systematically identify cell-type-specific RNA-associated proteins in mouse embryonic stem cells and finally, distribute our resource, rna.MAP, in an easy-to-use online interface (rna.proteincomplexes.org). Our system thus provides a methodology for explorations across human tissues, disease states, and throughout all domains of life.Entities:
Keywords: DIF-FRAC; RBP; RNA-binding protein; RNP; biochemical fractionation; interactome; mass spectrometry; protein complexes; proteomics; ribonucleoprotein complex
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Year: 2019 PMID: 31665645 PMCID: PMC6873818 DOI: 10.1016/j.celrep.2019.09.060
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423