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Systematic Discovery of Endogenous Human Ribonucleoprotein Complexes
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 investi...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6873818/ https://www.ncbi.nlm.nih.gov/pubmed/31665645 http://dx.doi.org/10.1016/j.celrep.2019.09.060 |
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author | Mallam, Anna L. Sae-Lee, Wisath Schaub, Jeffrey M. Tu, Fan Battenhouse, Anna Jang, Yu Jin Kim, Jonghwan Wallingford, John B. Finkelstein, Ilya J. Marcotte, Edward M. Drew, Kevin |
author_facet | Mallam, Anna L. Sae-Lee, Wisath Schaub, Jeffrey M. Tu, Fan Battenhouse, Anna Jang, Yu Jin Kim, Jonghwan Wallingford, John B. Finkelstein, Ilya J. Marcotte, Edward M. Drew, Kevin |
author_sort | Mallam, Anna L. |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-6873818 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
record_format | MEDLINE/PubMed |
spelling | pubmed-68738182019-11-22 Systematic Discovery of Endogenous Human Ribonucleoprotein Complexes Mallam, Anna L. Sae-Lee, Wisath Schaub, Jeffrey M. Tu, Fan Battenhouse, Anna Jang, Yu Jin Kim, Jonghwan Wallingford, John B. Finkelstein, Ilya J. Marcotte, Edward M. Drew, Kevin Cell Rep Article 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. 2019-10-29 /pmc/articles/PMC6873818/ /pubmed/31665645 http://dx.doi.org/10.1016/j.celrep.2019.09.060 Text en This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Mallam, Anna L. Sae-Lee, Wisath Schaub, Jeffrey M. Tu, Fan Battenhouse, Anna Jang, Yu Jin Kim, Jonghwan Wallingford, John B. Finkelstein, Ilya J. Marcotte, Edward M. Drew, Kevin Systematic Discovery of Endogenous Human Ribonucleoprotein Complexes |
title | Systematic Discovery of Endogenous Human Ribonucleoprotein Complexes |
title_full | Systematic Discovery of Endogenous Human Ribonucleoprotein Complexes |
title_fullStr | Systematic Discovery of Endogenous Human Ribonucleoprotein Complexes |
title_full_unstemmed | Systematic Discovery of Endogenous Human Ribonucleoprotein Complexes |
title_short | Systematic Discovery of Endogenous Human Ribonucleoprotein Complexes |
title_sort | systematic discovery of endogenous human ribonucleoprotein complexes |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6873818/ https://www.ncbi.nlm.nih.gov/pubmed/31665645 http://dx.doi.org/10.1016/j.celrep.2019.09.060 |
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