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MxB impedes the NUP358-mediated HIV-1 pre-integration complex nuclear import and viral replication cooperatively with CPSF6

BACKGROUND: The human myxovirus resistance 2 (Mx2/MxB) protein was originally found to regulate cytoplasmic-nuclear transport but was recently reported to restrict HIV-1 replication by binding to HIV-1 capsid (CA), preventing uncoating, the nuclear import of pre-integration complex (PIC) and viral D...

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Autores principales: Xie, Linlin, Chen, Lang, Zhong, Chaojie, Yu, Ting, Ju, Zhao, Wang, Meirong, Xiong, Hairong, Zeng, Yan, Wang, Jianhua, Hu, Haitao, Hou, Wei, Feng, Yong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7322711/
https://www.ncbi.nlm.nih.gov/pubmed/32600399
http://dx.doi.org/10.1186/s12977-020-00524-2
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author Xie, Linlin
Chen, Lang
Zhong, Chaojie
Yu, Ting
Ju, Zhao
Wang, Meirong
Xiong, Hairong
Zeng, Yan
Wang, Jianhua
Hu, Haitao
Hou, Wei
Feng, Yong
author_facet Xie, Linlin
Chen, Lang
Zhong, Chaojie
Yu, Ting
Ju, Zhao
Wang, Meirong
Xiong, Hairong
Zeng, Yan
Wang, Jianhua
Hu, Haitao
Hou, Wei
Feng, Yong
author_sort Xie, Linlin
collection PubMed
description BACKGROUND: The human myxovirus resistance 2 (Mx2/MxB) protein was originally found to regulate cytoplasmic-nuclear transport but was recently reported to restrict HIV-1 replication by binding to HIV-1 capsid (CA), preventing uncoating, the nuclear import of pre-integration complex (PIC) and viral DNA integration. This work explores the mechanisms of MxB-mediated HIV-1 inhibition. RESULTS: We demonstrated that MxB represses NUP358-mediated PIC nuclear import and HIV-1 replication. Moreover, MxB’s effects on PIC nuclear import and HIV-1 replication depend critically on cofactor cleavage and polyadenylation specificity factor subunit 6 (CPSF6). MxB binds nucleoporin NUP358, blocks NUP358-CA interaction, thereby impeding the nuclear import of HIV-1 PIC with CPSF6 binding to PIC. More intriguingly, CPSF6’s role in nuclear import depends on MxB, being a facilitator of HIV-1 nuclear import on its own, but becoming an inhibitor when MxB is present. CONCLUSIONS: Our work establishes that MxB impedes the NUP358-mediated HIV-1 nuclear import and viral replication cooperatively with CPSF6.
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spelling pubmed-73227112020-06-29 MxB impedes the NUP358-mediated HIV-1 pre-integration complex nuclear import and viral replication cooperatively with CPSF6 Xie, Linlin Chen, Lang Zhong, Chaojie Yu, Ting Ju, Zhao Wang, Meirong Xiong, Hairong Zeng, Yan Wang, Jianhua Hu, Haitao Hou, Wei Feng, Yong Retrovirology Research BACKGROUND: The human myxovirus resistance 2 (Mx2/MxB) protein was originally found to regulate cytoplasmic-nuclear transport but was recently reported to restrict HIV-1 replication by binding to HIV-1 capsid (CA), preventing uncoating, the nuclear import of pre-integration complex (PIC) and viral DNA integration. This work explores the mechanisms of MxB-mediated HIV-1 inhibition. RESULTS: We demonstrated that MxB represses NUP358-mediated PIC nuclear import and HIV-1 replication. Moreover, MxB’s effects on PIC nuclear import and HIV-1 replication depend critically on cofactor cleavage and polyadenylation specificity factor subunit 6 (CPSF6). MxB binds nucleoporin NUP358, blocks NUP358-CA interaction, thereby impeding the nuclear import of HIV-1 PIC with CPSF6 binding to PIC. More intriguingly, CPSF6’s role in nuclear import depends on MxB, being a facilitator of HIV-1 nuclear import on its own, but becoming an inhibitor when MxB is present. CONCLUSIONS: Our work establishes that MxB impedes the NUP358-mediated HIV-1 nuclear import and viral replication cooperatively with CPSF6. BioMed Central 2020-06-29 /pmc/articles/PMC7322711/ /pubmed/32600399 http://dx.doi.org/10.1186/s12977-020-00524-2 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Xie, Linlin
Chen, Lang
Zhong, Chaojie
Yu, Ting
Ju, Zhao
Wang, Meirong
Xiong, Hairong
Zeng, Yan
Wang, Jianhua
Hu, Haitao
Hou, Wei
Feng, Yong
MxB impedes the NUP358-mediated HIV-1 pre-integration complex nuclear import and viral replication cooperatively with CPSF6
title MxB impedes the NUP358-mediated HIV-1 pre-integration complex nuclear import and viral replication cooperatively with CPSF6
title_full MxB impedes the NUP358-mediated HIV-1 pre-integration complex nuclear import and viral replication cooperatively with CPSF6
title_fullStr MxB impedes the NUP358-mediated HIV-1 pre-integration complex nuclear import and viral replication cooperatively with CPSF6
title_full_unstemmed MxB impedes the NUP358-mediated HIV-1 pre-integration complex nuclear import and viral replication cooperatively with CPSF6
title_short MxB impedes the NUP358-mediated HIV-1 pre-integration complex nuclear import and viral replication cooperatively with CPSF6
title_sort mxb impedes the nup358-mediated hiv-1 pre-integration complex nuclear import and viral replication cooperatively with cpsf6
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7322711/
https://www.ncbi.nlm.nih.gov/pubmed/32600399
http://dx.doi.org/10.1186/s12977-020-00524-2
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