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Nuclear export of plant pararetrovirus mRNAs involves the TREX complex, two viral proteins and the highly structured 5′ leader region

In eukaryotes, the major nuclear export pathway for mature mRNAs uses the dimeric receptor TAP/p15, which is recruited to mRNAs via the multisubunit TREX complex, comprising the THO core and different export adaptors. Viruses that replicate in the nucleus adopt different strategies to hijack cellula...

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Autores principales: Kubina, Julie, Geldreich, Angèle, Gales, Jón Pol, Baumberger, Nicolas, Bouton, Clément, Ryabova, Lyubov A, Grasser, Klaus D, Keller, Mario, Dimitrova, Maria
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8421220/
https://www.ncbi.nlm.nih.gov/pubmed/34370034
http://dx.doi.org/10.1093/nar/gkab653
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author Kubina, Julie
Geldreich, Angèle
Gales, Jón Pol
Baumberger, Nicolas
Bouton, Clément
Ryabova, Lyubov A
Grasser, Klaus D
Keller, Mario
Dimitrova, Maria
author_facet Kubina, Julie
Geldreich, Angèle
Gales, Jón Pol
Baumberger, Nicolas
Bouton, Clément
Ryabova, Lyubov A
Grasser, Klaus D
Keller, Mario
Dimitrova, Maria
author_sort Kubina, Julie
collection PubMed
description In eukaryotes, the major nuclear export pathway for mature mRNAs uses the dimeric receptor TAP/p15, which is recruited to mRNAs via the multisubunit TREX complex, comprising the THO core and different export adaptors. Viruses that replicate in the nucleus adopt different strategies to hijack cellular export factors and achieve cytoplasmic translation of their mRNAs. No export receptors are known in plants, but Arabidopsis TREX resembles the mammalian complex, with a conserved hexameric THO core associated with ALY and UIEF proteins, as well as UAP56 and MOS11. The latter protein is an orthologue of mammalian CIP29. The nuclear export mechanism for viral mRNAs has not been described in plants. To understand this process, we investigated the export of mRNAs of the pararetrovirus CaMV in Arabidopsis and demonstrated that it is inhibited in plants deficient in ALY, MOS11 and/or TEX1. Deficiency for these factors renders plants partially resistant to CaMV infection. Two CaMV proteins, the coat protein P4 and reverse transcriptase P5, are important for nuclear export. P4 and P5 interact and co-localise in the nucleus with the cellular export factor MOS11. The highly structured 5′ leader region of 35S RNAs was identified as an export enhancing element that interacts with ALY1, ALY3 and MOS11 in vitro.
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spelling pubmed-84212202021-09-09 Nuclear export of plant pararetrovirus mRNAs involves the TREX complex, two viral proteins and the highly structured 5′ leader region Kubina, Julie Geldreich, Angèle Gales, Jón Pol Baumberger, Nicolas Bouton, Clément Ryabova, Lyubov A Grasser, Klaus D Keller, Mario Dimitrova, Maria Nucleic Acids Res RNA and RNA-protein complexes In eukaryotes, the major nuclear export pathway for mature mRNAs uses the dimeric receptor TAP/p15, which is recruited to mRNAs via the multisubunit TREX complex, comprising the THO core and different export adaptors. Viruses that replicate in the nucleus adopt different strategies to hijack cellular export factors and achieve cytoplasmic translation of their mRNAs. No export receptors are known in plants, but Arabidopsis TREX resembles the mammalian complex, with a conserved hexameric THO core associated with ALY and UIEF proteins, as well as UAP56 and MOS11. The latter protein is an orthologue of mammalian CIP29. The nuclear export mechanism for viral mRNAs has not been described in plants. To understand this process, we investigated the export of mRNAs of the pararetrovirus CaMV in Arabidopsis and demonstrated that it is inhibited in plants deficient in ALY, MOS11 and/or TEX1. Deficiency for these factors renders plants partially resistant to CaMV infection. Two CaMV proteins, the coat protein P4 and reverse transcriptase P5, are important for nuclear export. P4 and P5 interact and co-localise in the nucleus with the cellular export factor MOS11. The highly structured 5′ leader region of 35S RNAs was identified as an export enhancing element that interacts with ALY1, ALY3 and MOS11 in vitro. Oxford University Press 2021-08-09 /pmc/articles/PMC8421220/ /pubmed/34370034 http://dx.doi.org/10.1093/nar/gkab653 Text en © The Author(s) 2021. Published by Oxford University Press on behalf of Nucleic Acids Research. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle RNA and RNA-protein complexes
Kubina, Julie
Geldreich, Angèle
Gales, Jón Pol
Baumberger, Nicolas
Bouton, Clément
Ryabova, Lyubov A
Grasser, Klaus D
Keller, Mario
Dimitrova, Maria
Nuclear export of plant pararetrovirus mRNAs involves the TREX complex, two viral proteins and the highly structured 5′ leader region
title Nuclear export of plant pararetrovirus mRNAs involves the TREX complex, two viral proteins and the highly structured 5′ leader region
title_full Nuclear export of plant pararetrovirus mRNAs involves the TREX complex, two viral proteins and the highly structured 5′ leader region
title_fullStr Nuclear export of plant pararetrovirus mRNAs involves the TREX complex, two viral proteins and the highly structured 5′ leader region
title_full_unstemmed Nuclear export of plant pararetrovirus mRNAs involves the TREX complex, two viral proteins and the highly structured 5′ leader region
title_short Nuclear export of plant pararetrovirus mRNAs involves the TREX complex, two viral proteins and the highly structured 5′ leader region
title_sort nuclear export of plant pararetrovirus mrnas involves the trex complex, two viral proteins and the highly structured 5′ leader region
topic RNA and RNA-protein complexes
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8421220/
https://www.ncbi.nlm.nih.gov/pubmed/34370034
http://dx.doi.org/10.1093/nar/gkab653
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