Cargando…
Multiple nuclear-replicating viruses require the stress-induced protein ZC3H11A for efficient growth
The zinc finger CCCH-type containing 11A (ZC3H11A) gene encodes a well-conserved zinc finger protein that may function in mRNA export as it has been shown to associate with the transcription export (TREX) complex in proteomic screens. Here, we report that ZC3H11A is a stress-induced nuclear protein...
Autores principales: | , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
National Academy of Sciences
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5910864/ https://www.ncbi.nlm.nih.gov/pubmed/29610341 http://dx.doi.org/10.1073/pnas.1722333115 |
_version_ | 1783316128705019904 |
---|---|
author | Younis, Shady Kamel, Wael Falkeborn, Tina Wang, Hao Yu, Di Daniels, Robert Essand, Magnus Hinkula, Jorma Akusjärvi, Göran Andersson, Leif |
author_facet | Younis, Shady Kamel, Wael Falkeborn, Tina Wang, Hao Yu, Di Daniels, Robert Essand, Magnus Hinkula, Jorma Akusjärvi, Göran Andersson, Leif |
author_sort | Younis, Shady |
collection | PubMed |
description | The zinc finger CCCH-type containing 11A (ZC3H11A) gene encodes a well-conserved zinc finger protein that may function in mRNA export as it has been shown to associate with the transcription export (TREX) complex in proteomic screens. Here, we report that ZC3H11A is a stress-induced nuclear protein with RNA-binding capacity that localizes to nuclear splicing speckles. During an adenovirus infection, the ZC3H11A protein and splicing factor SRSF2 relocalize to nuclear regions where viral DNA replication and transcription take place. Knockout (KO) of ZC3H11A in HeLa cells demonstrated that several nuclear-replicating viruses are dependent on ZC3H11A for efficient growth (HIV, influenza virus, herpes simplex virus, and adenovirus), whereas cytoplasmic replicating viruses are not (vaccinia virus and Semliki Forest virus). High-throughput sequencing of ZC3H11A–cross-linked RNA showed that ZC3H11A binds to short purine-rich ribonucleotide stretches in cellular and adenoviral transcripts. We show that the RNA-binding property of ZC3H11A is crucial for its function and localization. In ZC3H11A KO cells, the adenovirus fiber mRNA accumulates in the cell nucleus. Our results suggest that ZC3H11A is important for maintaining nuclear export of mRNAs during stress and that several nuclear-replicating viruses take advantage of this mechanism to facilitate their replication. |
format | Online Article Text |
id | pubmed-5910864 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | National Academy of Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-59108642018-04-25 Multiple nuclear-replicating viruses require the stress-induced protein ZC3H11A for efficient growth Younis, Shady Kamel, Wael Falkeborn, Tina Wang, Hao Yu, Di Daniels, Robert Essand, Magnus Hinkula, Jorma Akusjärvi, Göran Andersson, Leif Proc Natl Acad Sci U S A PNAS Plus The zinc finger CCCH-type containing 11A (ZC3H11A) gene encodes a well-conserved zinc finger protein that may function in mRNA export as it has been shown to associate with the transcription export (TREX) complex in proteomic screens. Here, we report that ZC3H11A is a stress-induced nuclear protein with RNA-binding capacity that localizes to nuclear splicing speckles. During an adenovirus infection, the ZC3H11A protein and splicing factor SRSF2 relocalize to nuclear regions where viral DNA replication and transcription take place. Knockout (KO) of ZC3H11A in HeLa cells demonstrated that several nuclear-replicating viruses are dependent on ZC3H11A for efficient growth (HIV, influenza virus, herpes simplex virus, and adenovirus), whereas cytoplasmic replicating viruses are not (vaccinia virus and Semliki Forest virus). High-throughput sequencing of ZC3H11A–cross-linked RNA showed that ZC3H11A binds to short purine-rich ribonucleotide stretches in cellular and adenoviral transcripts. We show that the RNA-binding property of ZC3H11A is crucial for its function and localization. In ZC3H11A KO cells, the adenovirus fiber mRNA accumulates in the cell nucleus. Our results suggest that ZC3H11A is important for maintaining nuclear export of mRNAs during stress and that several nuclear-replicating viruses take advantage of this mechanism to facilitate their replication. National Academy of Sciences 2018-04-17 2018-04-02 /pmc/articles/PMC5910864/ /pubmed/29610341 http://dx.doi.org/10.1073/pnas.1722333115 Text en Copyright © 2018 the Author(s). Published by PNAS. https://creativecommons.org/licenses/by-nc-nd/4.0/ This open access article is distributed under Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) . |
spellingShingle | PNAS Plus Younis, Shady Kamel, Wael Falkeborn, Tina Wang, Hao Yu, Di Daniels, Robert Essand, Magnus Hinkula, Jorma Akusjärvi, Göran Andersson, Leif Multiple nuclear-replicating viruses require the stress-induced protein ZC3H11A for efficient growth |
title | Multiple nuclear-replicating viruses require the stress-induced protein ZC3H11A for efficient growth |
title_full | Multiple nuclear-replicating viruses require the stress-induced protein ZC3H11A for efficient growth |
title_fullStr | Multiple nuclear-replicating viruses require the stress-induced protein ZC3H11A for efficient growth |
title_full_unstemmed | Multiple nuclear-replicating viruses require the stress-induced protein ZC3H11A for efficient growth |
title_short | Multiple nuclear-replicating viruses require the stress-induced protein ZC3H11A for efficient growth |
title_sort | multiple nuclear-replicating viruses require the stress-induced protein zc3h11a for efficient growth |
topic | PNAS Plus |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5910864/ https://www.ncbi.nlm.nih.gov/pubmed/29610341 http://dx.doi.org/10.1073/pnas.1722333115 |
work_keys_str_mv | AT younisshady multiplenuclearreplicatingvirusesrequirethestressinducedproteinzc3h11aforefficientgrowth AT kamelwael multiplenuclearreplicatingvirusesrequirethestressinducedproteinzc3h11aforefficientgrowth AT falkeborntina multiplenuclearreplicatingvirusesrequirethestressinducedproteinzc3h11aforefficientgrowth AT wanghao multiplenuclearreplicatingvirusesrequirethestressinducedproteinzc3h11aforefficientgrowth AT yudi multiplenuclearreplicatingvirusesrequirethestressinducedproteinzc3h11aforefficientgrowth AT danielsrobert multiplenuclearreplicatingvirusesrequirethestressinducedproteinzc3h11aforefficientgrowth AT essandmagnus multiplenuclearreplicatingvirusesrequirethestressinducedproteinzc3h11aforefficientgrowth AT hinkulajorma multiplenuclearreplicatingvirusesrequirethestressinducedproteinzc3h11aforefficientgrowth AT akusjarvigoran multiplenuclearreplicatingvirusesrequirethestressinducedproteinzc3h11aforefficientgrowth AT anderssonleif multiplenuclearreplicatingvirusesrequirethestressinducedproteinzc3h11aforefficientgrowth |