Cargando…

Nuclear and Nucleolar Localization of Bovine Adenovirus-3 Protein V

The L2 region of bovine adenovirus-3 (BAdV-3) encodes a Mastadenovirus genus-specific protein, designated as pV, which is important for the production of progeny viruses. Here, we demonstrate that BAdV-3 pV, expressed as 55 kDa protein, localizes to the nucleus and specifically targets nucleolus of...

Descripción completa

Detalles Bibliográficos
Autores principales: Zhao, Xin, Tikoo, Suresh K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7815533/
https://www.ncbi.nlm.nih.gov/pubmed/33488533
http://dx.doi.org/10.3389/fmicb.2020.579593
_version_ 1783638248896069632
author Zhao, Xin
Tikoo, Suresh K.
author_facet Zhao, Xin
Tikoo, Suresh K.
author_sort Zhao, Xin
collection PubMed
description The L2 region of bovine adenovirus-3 (BAdV-3) encodes a Mastadenovirus genus-specific protein, designated as pV, which is important for the production of progeny viruses. Here, we demonstrate that BAdV-3 pV, expressed as 55 kDa protein, localizes to the nucleus and specifically targets nucleolus of the infected cells. Analysis of deletion mutants of pV suggested that amino acids 81–120, 190–210, and 380–389 act as multiple nuclear localization signals (NLS), which also appear to serve as the binding sites for importin α-3 protein, a member of the importin α/β nuclear import receptor pathway. Moreover, pV amino acids 21–50 and 380–389 appear to act as nucleolar localization signals (NoLs). Interestingly, amino acids 380–389 appear to act both as NLS and as NoLS. The presence of NoLS is essential for the production of infectious progeny virions, as deletion of both NoLs are lethal for the production of infectious BAdV-3. Analysis of mutant BAV.pVd1d3 (isolated in pV completing CRL cells) containing deletion/mutation of both NoLS in non-complementing CRL cells not only revealed the altered intracellular localization of mutant pV but also reduced the expression of some late proteins. However, it does not appear to affect the incorporation of viral proteins, including mutant pV, in BAV.pVd1d3 virions. Further analysis of CsCl purified BAV.pVd1d3 suggested the presence of thermo-labile virions with disrupted capsids, which appear to affect the infectivity of the progeny virions. Our results suggest that pV contains overlapping and non-overlapping NoLS/NLS. Moreover, the presence of both NoLS appear essential for the production of stable and infectious progeny BAV.pVd1d3 virions.
format Online
Article
Text
id pubmed-7815533
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-78155332021-01-21 Nuclear and Nucleolar Localization of Bovine Adenovirus-3 Protein V Zhao, Xin Tikoo, Suresh K. Front Microbiol Microbiology The L2 region of bovine adenovirus-3 (BAdV-3) encodes a Mastadenovirus genus-specific protein, designated as pV, which is important for the production of progeny viruses. Here, we demonstrate that BAdV-3 pV, expressed as 55 kDa protein, localizes to the nucleus and specifically targets nucleolus of the infected cells. Analysis of deletion mutants of pV suggested that amino acids 81–120, 190–210, and 380–389 act as multiple nuclear localization signals (NLS), which also appear to serve as the binding sites for importin α-3 protein, a member of the importin α/β nuclear import receptor pathway. Moreover, pV amino acids 21–50 and 380–389 appear to act as nucleolar localization signals (NoLs). Interestingly, amino acids 380–389 appear to act both as NLS and as NoLS. The presence of NoLS is essential for the production of infectious progeny virions, as deletion of both NoLs are lethal for the production of infectious BAdV-3. Analysis of mutant BAV.pVd1d3 (isolated in pV completing CRL cells) containing deletion/mutation of both NoLS in non-complementing CRL cells not only revealed the altered intracellular localization of mutant pV but also reduced the expression of some late proteins. However, it does not appear to affect the incorporation of viral proteins, including mutant pV, in BAV.pVd1d3 virions. Further analysis of CsCl purified BAV.pVd1d3 suggested the presence of thermo-labile virions with disrupted capsids, which appear to affect the infectivity of the progeny virions. Our results suggest that pV contains overlapping and non-overlapping NoLS/NLS. Moreover, the presence of both NoLS appear essential for the production of stable and infectious progeny BAV.pVd1d3 virions. Frontiers Media S.A. 2021-01-06 /pmc/articles/PMC7815533/ /pubmed/33488533 http://dx.doi.org/10.3389/fmicb.2020.579593 Text en Copyright © 2021 Zhao and Tikoo. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Zhao, Xin
Tikoo, Suresh K.
Nuclear and Nucleolar Localization of Bovine Adenovirus-3 Protein V
title Nuclear and Nucleolar Localization of Bovine Adenovirus-3 Protein V
title_full Nuclear and Nucleolar Localization of Bovine Adenovirus-3 Protein V
title_fullStr Nuclear and Nucleolar Localization of Bovine Adenovirus-3 Protein V
title_full_unstemmed Nuclear and Nucleolar Localization of Bovine Adenovirus-3 Protein V
title_short Nuclear and Nucleolar Localization of Bovine Adenovirus-3 Protein V
title_sort nuclear and nucleolar localization of bovine adenovirus-3 protein v
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7815533/
https://www.ncbi.nlm.nih.gov/pubmed/33488533
http://dx.doi.org/10.3389/fmicb.2020.579593
work_keys_str_mv AT zhaoxin nuclearandnucleolarlocalizationofbovineadenovirus3proteinv
AT tikoosureshk nuclearandnucleolarlocalizationofbovineadenovirus3proteinv