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An Interaction between KSHV ORF57 and UIF Provides mRNA-Adaptor Redundancy in Herpesvirus Intronless mRNA Export

The hTREX complex mediates cellular bulk mRNA nuclear export by recruiting the nuclear export factor, TAP, via a direct interaction with the export adaptor, Aly. Intriguingly however, depletion of Aly only leads to a modest reduction in cellular mRNA nuclear export, suggesting the existence of addit...

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Autores principales: Jackson, Brian R., Boyne, James R., Noerenberg, Marko, Taylor, Adam, Hautbergue, Guillaume M., Walsh, Matthew J., Wheat, Rachel, Blackbourn, David J., Wilson, Stuart A., Whitehouse, Adrian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3141038/
https://www.ncbi.nlm.nih.gov/pubmed/21814512
http://dx.doi.org/10.1371/journal.ppat.1002138
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author Jackson, Brian R.
Boyne, James R.
Noerenberg, Marko
Taylor, Adam
Hautbergue, Guillaume M.
Walsh, Matthew J.
Wheat, Rachel
Blackbourn, David J.
Wilson, Stuart A.
Whitehouse, Adrian
author_facet Jackson, Brian R.
Boyne, James R.
Noerenberg, Marko
Taylor, Adam
Hautbergue, Guillaume M.
Walsh, Matthew J.
Wheat, Rachel
Blackbourn, David J.
Wilson, Stuart A.
Whitehouse, Adrian
author_sort Jackson, Brian R.
collection PubMed
description The hTREX complex mediates cellular bulk mRNA nuclear export by recruiting the nuclear export factor, TAP, via a direct interaction with the export adaptor, Aly. Intriguingly however, depletion of Aly only leads to a modest reduction in cellular mRNA nuclear export, suggesting the existence of additional mRNA nuclear export adaptor proteins. In order to efficiently export Kaposi's sarcoma-associated herpesvirus (KSHV) intronless mRNAs from the nucleus, the KSHV ORF57 protein recruits hTREX onto viral intronless mRNAs allowing access to the TAP-mediated export pathway. Similarly however, depletion of Aly only leads to a modest reduction in the nuclear export of KSHV intronless mRNAs. Herein, we identify a novel interaction between ORF57 and the cellular protein, UIF. We provide the first evidence that the ORF57-UIF interaction enables the recruitment of hTREX and TAP to KSHV intronless mRNAs in Aly-depleted cells. Strikingly, depletion of both Aly and UIF inhibits the formation of an ORF57-mediated nuclear export competent ribonucleoprotein particle and consequently prevents ORF57-mediated mRNA nuclear export and KSHV protein production. Importantly, these findings highlight that redundancy exists in the eukaryotic system for certain hTREX components involved in the mRNA nuclear export of intronless KSHV mRNAs.
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spelling pubmed-31410382011-08-03 An Interaction between KSHV ORF57 and UIF Provides mRNA-Adaptor Redundancy in Herpesvirus Intronless mRNA Export Jackson, Brian R. Boyne, James R. Noerenberg, Marko Taylor, Adam Hautbergue, Guillaume M. Walsh, Matthew J. Wheat, Rachel Blackbourn, David J. Wilson, Stuart A. Whitehouse, Adrian PLoS Pathog Research Article The hTREX complex mediates cellular bulk mRNA nuclear export by recruiting the nuclear export factor, TAP, via a direct interaction with the export adaptor, Aly. Intriguingly however, depletion of Aly only leads to a modest reduction in cellular mRNA nuclear export, suggesting the existence of additional mRNA nuclear export adaptor proteins. In order to efficiently export Kaposi's sarcoma-associated herpesvirus (KSHV) intronless mRNAs from the nucleus, the KSHV ORF57 protein recruits hTREX onto viral intronless mRNAs allowing access to the TAP-mediated export pathway. Similarly however, depletion of Aly only leads to a modest reduction in the nuclear export of KSHV intronless mRNAs. Herein, we identify a novel interaction between ORF57 and the cellular protein, UIF. We provide the first evidence that the ORF57-UIF interaction enables the recruitment of hTREX and TAP to KSHV intronless mRNAs in Aly-depleted cells. Strikingly, depletion of both Aly and UIF inhibits the formation of an ORF57-mediated nuclear export competent ribonucleoprotein particle and consequently prevents ORF57-mediated mRNA nuclear export and KSHV protein production. Importantly, these findings highlight that redundancy exists in the eukaryotic system for certain hTREX components involved in the mRNA nuclear export of intronless KSHV mRNAs. Public Library of Science 2011-07-21 /pmc/articles/PMC3141038/ /pubmed/21814512 http://dx.doi.org/10.1371/journal.ppat.1002138 Text en Jackson et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Jackson, Brian R.
Boyne, James R.
Noerenberg, Marko
Taylor, Adam
Hautbergue, Guillaume M.
Walsh, Matthew J.
Wheat, Rachel
Blackbourn, David J.
Wilson, Stuart A.
Whitehouse, Adrian
An Interaction between KSHV ORF57 and UIF Provides mRNA-Adaptor Redundancy in Herpesvirus Intronless mRNA Export
title An Interaction between KSHV ORF57 and UIF Provides mRNA-Adaptor Redundancy in Herpesvirus Intronless mRNA Export
title_full An Interaction between KSHV ORF57 and UIF Provides mRNA-Adaptor Redundancy in Herpesvirus Intronless mRNA Export
title_fullStr An Interaction between KSHV ORF57 and UIF Provides mRNA-Adaptor Redundancy in Herpesvirus Intronless mRNA Export
title_full_unstemmed An Interaction between KSHV ORF57 and UIF Provides mRNA-Adaptor Redundancy in Herpesvirus Intronless mRNA Export
title_short An Interaction between KSHV ORF57 and UIF Provides mRNA-Adaptor Redundancy in Herpesvirus Intronless mRNA Export
title_sort interaction between kshv orf57 and uif provides mrna-adaptor redundancy in herpesvirus intronless mrna export
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3141038/
https://www.ncbi.nlm.nih.gov/pubmed/21814512
http://dx.doi.org/10.1371/journal.ppat.1002138
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