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CCR4, a RNA decay factor, is hijacked by a plant cytorhabdovirus phosphoprotein to facilitate virus replication
Carbon catabolite repression 4 (CCR4) is a conserved mRNA deadenylase regulating posttranscriptional gene expression. However, regulation of CCR4 in virus infections is less understood. Here, we characterized a pro-viral role of CCR4 in replication of a plant cytorhabdovirus, Barley yellow striate m...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7105381/ https://www.ncbi.nlm.nih.gov/pubmed/32207684 http://dx.doi.org/10.7554/eLife.53753 |
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author | Zhang, Zhen-Jia Gao, Qiang Fang, Xiao-Dong Ding, Zhi-Hang Gao, Dong-Min Xu, Wen-Ya Cao, Qing Qiao, Ji-Hui Yang, Yi-Zhou Han, Chenggui Wang, Ying Yuan, Xuefeng Li, Dawei Wang, Xian-Bing |
author_facet | Zhang, Zhen-Jia Gao, Qiang Fang, Xiao-Dong Ding, Zhi-Hang Gao, Dong-Min Xu, Wen-Ya Cao, Qing Qiao, Ji-Hui Yang, Yi-Zhou Han, Chenggui Wang, Ying Yuan, Xuefeng Li, Dawei Wang, Xian-Bing |
author_sort | Zhang, Zhen-Jia |
collection | PubMed |
description | Carbon catabolite repression 4 (CCR4) is a conserved mRNA deadenylase regulating posttranscriptional gene expression. However, regulation of CCR4 in virus infections is less understood. Here, we characterized a pro-viral role of CCR4 in replication of a plant cytorhabdovirus, Barley yellow striate mosaic virus (BYSMV). The barley (Hordeum vulgare) CCR4 protein (HvCCR4) was identified to interact with the BYSMV phosphoprotein (P). The BYSMV P protein recruited HvCCR4 from processing bodies (PBs) into viroplasm-like bodies. Overexpression of HvCCR4 promoted BYSMV replication in plants. Conversely, knockdown of the small brown planthopper CCR4 inhibited viral accumulation in the insect vector. Biochemistry experiments revealed that HvCCR4 was recruited into N–RNA complexes by the BYSMV P protein and triggered turnover of N-bound cellular mRNAs, thereby releasing RNA-free N protein to bind viral genomic RNA for optimal viral replication. Our results demonstrate that the co-opted CCR4-mediated RNA decay facilitates cytorhabdovirus replication in plants and insects. |
format | Online Article Text |
id | pubmed-7105381 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-71053812020-04-01 CCR4, a RNA decay factor, is hijacked by a plant cytorhabdovirus phosphoprotein to facilitate virus replication Zhang, Zhen-Jia Gao, Qiang Fang, Xiao-Dong Ding, Zhi-Hang Gao, Dong-Min Xu, Wen-Ya Cao, Qing Qiao, Ji-Hui Yang, Yi-Zhou Han, Chenggui Wang, Ying Yuan, Xuefeng Li, Dawei Wang, Xian-Bing eLife Microbiology and Infectious Disease Carbon catabolite repression 4 (CCR4) is a conserved mRNA deadenylase regulating posttranscriptional gene expression. However, regulation of CCR4 in virus infections is less understood. Here, we characterized a pro-viral role of CCR4 in replication of a plant cytorhabdovirus, Barley yellow striate mosaic virus (BYSMV). The barley (Hordeum vulgare) CCR4 protein (HvCCR4) was identified to interact with the BYSMV phosphoprotein (P). The BYSMV P protein recruited HvCCR4 from processing bodies (PBs) into viroplasm-like bodies. Overexpression of HvCCR4 promoted BYSMV replication in plants. Conversely, knockdown of the small brown planthopper CCR4 inhibited viral accumulation in the insect vector. Biochemistry experiments revealed that HvCCR4 was recruited into N–RNA complexes by the BYSMV P protein and triggered turnover of N-bound cellular mRNAs, thereby releasing RNA-free N protein to bind viral genomic RNA for optimal viral replication. Our results demonstrate that the co-opted CCR4-mediated RNA decay facilitates cytorhabdovirus replication in plants and insects. eLife Sciences Publications, Ltd 2020-03-24 /pmc/articles/PMC7105381/ /pubmed/32207684 http://dx.doi.org/10.7554/eLife.53753 Text en © 2020, Zhang et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Microbiology and Infectious Disease Zhang, Zhen-Jia Gao, Qiang Fang, Xiao-Dong Ding, Zhi-Hang Gao, Dong-Min Xu, Wen-Ya Cao, Qing Qiao, Ji-Hui Yang, Yi-Zhou Han, Chenggui Wang, Ying Yuan, Xuefeng Li, Dawei Wang, Xian-Bing CCR4, a RNA decay factor, is hijacked by a plant cytorhabdovirus phosphoprotein to facilitate virus replication |
title | CCR4, a RNA decay factor, is hijacked by a plant cytorhabdovirus phosphoprotein to facilitate virus replication |
title_full | CCR4, a RNA decay factor, is hijacked by a plant cytorhabdovirus phosphoprotein to facilitate virus replication |
title_fullStr | CCR4, a RNA decay factor, is hijacked by a plant cytorhabdovirus phosphoprotein to facilitate virus replication |
title_full_unstemmed | CCR4, a RNA decay factor, is hijacked by a plant cytorhabdovirus phosphoprotein to facilitate virus replication |
title_short | CCR4, a RNA decay factor, is hijacked by a plant cytorhabdovirus phosphoprotein to facilitate virus replication |
title_sort | ccr4, a rna decay factor, is hijacked by a plant cytorhabdovirus phosphoprotein to facilitate virus replication |
topic | Microbiology and Infectious Disease |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7105381/ https://www.ncbi.nlm.nih.gov/pubmed/32207684 http://dx.doi.org/10.7554/eLife.53753 |
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