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Uncovering viral RNA–host cell interactions on a proteome-wide scale

RNA viruses interact with a wide range of cellular RNA-binding proteins (RBPs) during their life cycle. The prevalence of these host–virus interactions has been highlighted by new methods that elucidate the composition of viral ribonucleoproteins (vRNPs). Applied to 11 viruses so far, these approach...

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Autores principales: Iselin, Louisa, Palmalux, Natasha, Kamel, Wael, Simmonds, Peter, Mohammed, Shabaz, Castello, Alfredo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Trends Journals 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9187521/
https://www.ncbi.nlm.nih.gov/pubmed/34509361
http://dx.doi.org/10.1016/j.tibs.2021.08.002
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author Iselin, Louisa
Palmalux, Natasha
Kamel, Wael
Simmonds, Peter
Mohammed, Shabaz
Castello, Alfredo
author_facet Iselin, Louisa
Palmalux, Natasha
Kamel, Wael
Simmonds, Peter
Mohammed, Shabaz
Castello, Alfredo
author_sort Iselin, Louisa
collection PubMed
description RNA viruses interact with a wide range of cellular RNA-binding proteins (RBPs) during their life cycle. The prevalence of these host–virus interactions has been highlighted by new methods that elucidate the composition of viral ribonucleoproteins (vRNPs). Applied to 11 viruses so far, these approaches have revealed hundreds of cellular RBPs that interact with viral (v)RNA in infected cells. However, consistency across methods is limited, raising questions about methodological considerations when designing and interpreting these studies. Here, we discuss these caveats and, through comparing available vRNA interactomes, describe RBPs that are consistently identified as vRNP components and outline their potential roles in infection. In summary, these novel approaches have uncovered a new universe of host–virus interactions holding great therapeutic potential.
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spelling pubmed-91875212022-06-14 Uncovering viral RNA–host cell interactions on a proteome-wide scale Iselin, Louisa Palmalux, Natasha Kamel, Wael Simmonds, Peter Mohammed, Shabaz Castello, Alfredo Trends Biochem Sci Review RNA viruses interact with a wide range of cellular RNA-binding proteins (RBPs) during their life cycle. The prevalence of these host–virus interactions has been highlighted by new methods that elucidate the composition of viral ribonucleoproteins (vRNPs). Applied to 11 viruses so far, these approaches have revealed hundreds of cellular RBPs that interact with viral (v)RNA in infected cells. However, consistency across methods is limited, raising questions about methodological considerations when designing and interpreting these studies. Here, we discuss these caveats and, through comparing available vRNA interactomes, describe RBPs that are consistently identified as vRNP components and outline their potential roles in infection. In summary, these novel approaches have uncovered a new universe of host–virus interactions holding great therapeutic potential. Elsevier Trends Journals 2022-01 /pmc/articles/PMC9187521/ /pubmed/34509361 http://dx.doi.org/10.1016/j.tibs.2021.08.002 Text en © 2021 The Authors https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Iselin, Louisa
Palmalux, Natasha
Kamel, Wael
Simmonds, Peter
Mohammed, Shabaz
Castello, Alfredo
Uncovering viral RNA–host cell interactions on a proteome-wide scale
title Uncovering viral RNA–host cell interactions on a proteome-wide scale
title_full Uncovering viral RNA–host cell interactions on a proteome-wide scale
title_fullStr Uncovering viral RNA–host cell interactions on a proteome-wide scale
title_full_unstemmed Uncovering viral RNA–host cell interactions on a proteome-wide scale
title_short Uncovering viral RNA–host cell interactions on a proteome-wide scale
title_sort uncovering viral rna–host cell interactions on a proteome-wide scale
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9187521/
https://www.ncbi.nlm.nih.gov/pubmed/34509361
http://dx.doi.org/10.1016/j.tibs.2021.08.002
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