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Parvovirus nonstructural protein 2 interacts with chromatin-regulating cellular proteins

Autonomous parvoviruses encode at least two nonstructural proteins, NS1 and NS2. While NS1 is linked to important nuclear processes required for viral replication, much less is known about the role of NS2. Specifically, the function of canine parvovirus (CPV) NS2 has remained undefined. Here we have...

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Autores principales: Mattola, Salla, Salokas, Kari, Aho, Vesa, Mäntylä, Elina, Salminen, Sami, Hakanen, Satu, Niskanen, Einari A., Svirskaite, Julija, Ihalainen, Teemu O., Airenne, Kari J., Kaikkonen-Määttä, Minna, Parrish, Colin R., Varjosalo, Markku, Vihinen-Ranta, Maija
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9020740/
https://www.ncbi.nlm.nih.gov/pubmed/35395063
http://dx.doi.org/10.1371/journal.ppat.1010353
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author Mattola, Salla
Salokas, Kari
Aho, Vesa
Mäntylä, Elina
Salminen, Sami
Hakanen, Satu
Niskanen, Einari A.
Svirskaite, Julija
Ihalainen, Teemu O.
Airenne, Kari J.
Kaikkonen-Määttä, Minna
Parrish, Colin R.
Varjosalo, Markku
Vihinen-Ranta, Maija
author_facet Mattola, Salla
Salokas, Kari
Aho, Vesa
Mäntylä, Elina
Salminen, Sami
Hakanen, Satu
Niskanen, Einari A.
Svirskaite, Julija
Ihalainen, Teemu O.
Airenne, Kari J.
Kaikkonen-Määttä, Minna
Parrish, Colin R.
Varjosalo, Markku
Vihinen-Ranta, Maija
author_sort Mattola, Salla
collection PubMed
description Autonomous parvoviruses encode at least two nonstructural proteins, NS1 and NS2. While NS1 is linked to important nuclear processes required for viral replication, much less is known about the role of NS2. Specifically, the function of canine parvovirus (CPV) NS2 has remained undefined. Here we have used proximity-dependent biotin identification (BioID) to screen for nuclear proteins that associate with CPV NS2. Many of these associations were seen both in noninfected and infected cells, however, the major type of interacting proteins shifted from nuclear envelope proteins to chromatin-associated proteins in infected cells. BioID interactions revealed a potential role for NS2 in DNA remodeling and damage response. Studies of mutant viral genomes with truncated forms of the NS2 protein suggested a change in host chromatin accessibility. Moreover, further studies with NS2 mutants indicated that NS2 performs functions that affect the quantity and distribution of proteins linked to DNA damage response. Notably, mutation in the splice donor site of the NS2 led to a preferred formation of small viral replication center foci instead of the large coalescent centers seen in wild-type infection. Collectively, our results provide insights into potential roles of CPV NS2 in controlling chromatin remodeling and DNA damage response during parvoviral replication.
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spelling pubmed-90207402022-04-21 Parvovirus nonstructural protein 2 interacts with chromatin-regulating cellular proteins Mattola, Salla Salokas, Kari Aho, Vesa Mäntylä, Elina Salminen, Sami Hakanen, Satu Niskanen, Einari A. Svirskaite, Julija Ihalainen, Teemu O. Airenne, Kari J. Kaikkonen-Määttä, Minna Parrish, Colin R. Varjosalo, Markku Vihinen-Ranta, Maija PLoS Pathog Research Article Autonomous parvoviruses encode at least two nonstructural proteins, NS1 and NS2. While NS1 is linked to important nuclear processes required for viral replication, much less is known about the role of NS2. Specifically, the function of canine parvovirus (CPV) NS2 has remained undefined. Here we have used proximity-dependent biotin identification (BioID) to screen for nuclear proteins that associate with CPV NS2. Many of these associations were seen both in noninfected and infected cells, however, the major type of interacting proteins shifted from nuclear envelope proteins to chromatin-associated proteins in infected cells. BioID interactions revealed a potential role for NS2 in DNA remodeling and damage response. Studies of mutant viral genomes with truncated forms of the NS2 protein suggested a change in host chromatin accessibility. Moreover, further studies with NS2 mutants indicated that NS2 performs functions that affect the quantity and distribution of proteins linked to DNA damage response. Notably, mutation in the splice donor site of the NS2 led to a preferred formation of small viral replication center foci instead of the large coalescent centers seen in wild-type infection. Collectively, our results provide insights into potential roles of CPV NS2 in controlling chromatin remodeling and DNA damage response during parvoviral replication. Public Library of Science 2022-04-08 /pmc/articles/PMC9020740/ /pubmed/35395063 http://dx.doi.org/10.1371/journal.ppat.1010353 Text en © 2022 Mattola et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Mattola, Salla
Salokas, Kari
Aho, Vesa
Mäntylä, Elina
Salminen, Sami
Hakanen, Satu
Niskanen, Einari A.
Svirskaite, Julija
Ihalainen, Teemu O.
Airenne, Kari J.
Kaikkonen-Määttä, Minna
Parrish, Colin R.
Varjosalo, Markku
Vihinen-Ranta, Maija
Parvovirus nonstructural protein 2 interacts with chromatin-regulating cellular proteins
title Parvovirus nonstructural protein 2 interacts with chromatin-regulating cellular proteins
title_full Parvovirus nonstructural protein 2 interacts with chromatin-regulating cellular proteins
title_fullStr Parvovirus nonstructural protein 2 interacts with chromatin-regulating cellular proteins
title_full_unstemmed Parvovirus nonstructural protein 2 interacts with chromatin-regulating cellular proteins
title_short Parvovirus nonstructural protein 2 interacts with chromatin-regulating cellular proteins
title_sort parvovirus nonstructural protein 2 interacts with chromatin-regulating cellular proteins
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9020740/
https://www.ncbi.nlm.nih.gov/pubmed/35395063
http://dx.doi.org/10.1371/journal.ppat.1010353
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