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Human proteins that interact with RNA/DNA hybrids

RNA/DNA hybrids form when RNA hybridizes with its template DNA generating a three-stranded structure known as the R-loop. Knowledge of how they form and resolve, as well as their functional roles, is limited. Here, by pull-down assays followed by mass spectrometry, we identified 803 proteins that bi...

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Autores principales: Wang, Isabel X., Grunseich, Christopher, Fox, Jennifer, Burdick, Joshua, Zhu, Zhengwei, Ravazian, Niema, Hafner, Markus, Cheung, Vivian G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6120628/
https://www.ncbi.nlm.nih.gov/pubmed/30108179
http://dx.doi.org/10.1101/gr.237362.118
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author Wang, Isabel X.
Grunseich, Christopher
Fox, Jennifer
Burdick, Joshua
Zhu, Zhengwei
Ravazian, Niema
Hafner, Markus
Cheung, Vivian G.
author_facet Wang, Isabel X.
Grunseich, Christopher
Fox, Jennifer
Burdick, Joshua
Zhu, Zhengwei
Ravazian, Niema
Hafner, Markus
Cheung, Vivian G.
author_sort Wang, Isabel X.
collection PubMed
description RNA/DNA hybrids form when RNA hybridizes with its template DNA generating a three-stranded structure known as the R-loop. Knowledge of how they form and resolve, as well as their functional roles, is limited. Here, by pull-down assays followed by mass spectrometry, we identified 803 proteins that bind to RNA/DNA hybrids. Because these proteins were identified using in vitro assays, we confirmed that they bind to R-loops in vivo. They include proteins that are involved in a variety of functions, including most steps of RNA processing. The proteins are enriched for K homology (KH) and helicase domains. Among them, more than 300 proteins preferred binding to hybrids than double-stranded DNA. These proteins serve as starting points for mechanistic studies to elucidate what RNA/DNA hybrids regulate and how they are regulated.
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spelling pubmed-61206282018-09-05 Human proteins that interact with RNA/DNA hybrids Wang, Isabel X. Grunseich, Christopher Fox, Jennifer Burdick, Joshua Zhu, Zhengwei Ravazian, Niema Hafner, Markus Cheung, Vivian G. Genome Res Resource RNA/DNA hybrids form when RNA hybridizes with its template DNA generating a three-stranded structure known as the R-loop. Knowledge of how they form and resolve, as well as their functional roles, is limited. Here, by pull-down assays followed by mass spectrometry, we identified 803 proteins that bind to RNA/DNA hybrids. Because these proteins were identified using in vitro assays, we confirmed that they bind to R-loops in vivo. They include proteins that are involved in a variety of functions, including most steps of RNA processing. The proteins are enriched for K homology (KH) and helicase domains. Among them, more than 300 proteins preferred binding to hybrids than double-stranded DNA. These proteins serve as starting points for mechanistic studies to elucidate what RNA/DNA hybrids regulate and how they are regulated. Cold Spring Harbor Laboratory Press 2018-09 /pmc/articles/PMC6120628/ /pubmed/30108179 http://dx.doi.org/10.1101/gr.237362.118 Text en © 2018 Wang et al.; Published by Cold Spring Harbor Laboratory Press http://creativecommons.org/licenses/by/4.0/ This article, published in Genome Research, is available under a Creative Commons License (Attribution 4.0 International), as described at http://creativecommons.org/licenses/by/4.0/.
spellingShingle Resource
Wang, Isabel X.
Grunseich, Christopher
Fox, Jennifer
Burdick, Joshua
Zhu, Zhengwei
Ravazian, Niema
Hafner, Markus
Cheung, Vivian G.
Human proteins that interact with RNA/DNA hybrids
title Human proteins that interact with RNA/DNA hybrids
title_full Human proteins that interact with RNA/DNA hybrids
title_fullStr Human proteins that interact with RNA/DNA hybrids
title_full_unstemmed Human proteins that interact with RNA/DNA hybrids
title_short Human proteins that interact with RNA/DNA hybrids
title_sort human proteins that interact with rna/dna hybrids
topic Resource
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6120628/
https://www.ncbi.nlm.nih.gov/pubmed/30108179
http://dx.doi.org/10.1101/gr.237362.118
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