Cargando…

Oligomerization of Uukuniemi virus nucleocapsid protein

BACKGROUND: Uukuniemi virus (UUKV) belongs to the Phlebovirus genus in the family Bunyaviridae. As a non-pathogenic virus for humans UUKV has served as a safe model bunyavirus in a number of studies addressing fundamental questions such as organization and regulation of viral genes, genome replicati...

Descripción completa

Detalles Bibliográficos
Autores principales: Katz, Anna, Freiberg, Alexander N, Backström, Vera, Schulz, Axel R, Mateos, Angelo, Holm, Liisa, Pettersson, Ralf F, Vaheri, Antti, Flick, Ramon, Plyusnin, Alexander
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2925374/
https://www.ncbi.nlm.nih.gov/pubmed/20698970
http://dx.doi.org/10.1186/1743-422X-7-187
_version_ 1782185673879453696
author Katz, Anna
Freiberg, Alexander N
Backström, Vera
Schulz, Axel R
Mateos, Angelo
Holm, Liisa
Pettersson, Ralf F
Vaheri, Antti
Flick, Ramon
Plyusnin, Alexander
author_facet Katz, Anna
Freiberg, Alexander N
Backström, Vera
Schulz, Axel R
Mateos, Angelo
Holm, Liisa
Pettersson, Ralf F
Vaheri, Antti
Flick, Ramon
Plyusnin, Alexander
author_sort Katz, Anna
collection PubMed
description BACKGROUND: Uukuniemi virus (UUKV) belongs to the Phlebovirus genus in the family Bunyaviridae. As a non-pathogenic virus for humans UUKV has served as a safe model bunyavirus in a number of studies addressing fundamental questions such as organization and regulation of viral genes, genome replication, structure and assembly. The present study is focused on the oligomerization of the UUKV nucleocapsid (N) protein, which plays an important role in several steps of virus replication. The aim was to locate the domains involved in the N protein oligomerization and study the process in detail. RESULTS: A set of experiments concentrating on the N- and C-termini of the protein was performed, first by completely or partially deleting putative N-N-interaction domains and then by introducing point mutations of amino acid residues. Mutagenesis strategy was based on the computer modeling of secondary and tertiary structure of the N protein. The N protein mutants were studied in chemical cross-linking, immunofluorescence, mammalian two-hybrid, minigenome, and virus-like particle-forming assays. The data showed that the oligomerization ability of UUKV-N protein depends on the presence of intact α-helices on both termini of the N protein molecule and that a specific structure in the N-terminal region plays a crucial role in the N-N interaction(s). This structure is formed by two α-helices, rich in amino acid residues with aromatic (W7, F10, W19, F27, F31) or long aliphatic (I14, I24) side chains. Furthermore, some of the N-terminal mutations (e.g. I14A, I24A, F31A) affected the N protein functionality both in mammalian two-hybrid and minigenome assays. CONCLUSIONS: UUKV-N protein has ability to form oligomers in chemical cross-linking and mammalian two-hybrid assays. In mutational analysis, some of the introduced single-point mutations abolished the N protein functionality both in mammalian two-hybrid and minigenome assays, suggesting that especially the N-terminal region of the UUKV-N protein is essential for the N-N interaction.
format Text
id pubmed-2925374
institution National Center for Biotechnology Information
language English
publishDate 2010
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-29253742010-08-24 Oligomerization of Uukuniemi virus nucleocapsid protein Katz, Anna Freiberg, Alexander N Backström, Vera Schulz, Axel R Mateos, Angelo Holm, Liisa Pettersson, Ralf F Vaheri, Antti Flick, Ramon Plyusnin, Alexander Virol J Research BACKGROUND: Uukuniemi virus (UUKV) belongs to the Phlebovirus genus in the family Bunyaviridae. As a non-pathogenic virus for humans UUKV has served as a safe model bunyavirus in a number of studies addressing fundamental questions such as organization and regulation of viral genes, genome replication, structure and assembly. The present study is focused on the oligomerization of the UUKV nucleocapsid (N) protein, which plays an important role in several steps of virus replication. The aim was to locate the domains involved in the N protein oligomerization and study the process in detail. RESULTS: A set of experiments concentrating on the N- and C-termini of the protein was performed, first by completely or partially deleting putative N-N-interaction domains and then by introducing point mutations of amino acid residues. Mutagenesis strategy was based on the computer modeling of secondary and tertiary structure of the N protein. The N protein mutants were studied in chemical cross-linking, immunofluorescence, mammalian two-hybrid, minigenome, and virus-like particle-forming assays. The data showed that the oligomerization ability of UUKV-N protein depends on the presence of intact α-helices on both termini of the N protein molecule and that a specific structure in the N-terminal region plays a crucial role in the N-N interaction(s). This structure is formed by two α-helices, rich in amino acid residues with aromatic (W7, F10, W19, F27, F31) or long aliphatic (I14, I24) side chains. Furthermore, some of the N-terminal mutations (e.g. I14A, I24A, F31A) affected the N protein functionality both in mammalian two-hybrid and minigenome assays. CONCLUSIONS: UUKV-N protein has ability to form oligomers in chemical cross-linking and mammalian two-hybrid assays. In mutational analysis, some of the introduced single-point mutations abolished the N protein functionality both in mammalian two-hybrid and minigenome assays, suggesting that especially the N-terminal region of the UUKV-N protein is essential for the N-N interaction. BioMed Central 2010-08-10 /pmc/articles/PMC2925374/ /pubmed/20698970 http://dx.doi.org/10.1186/1743-422X-7-187 Text en Copyright ©2010 Katz et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Katz, Anna
Freiberg, Alexander N
Backström, Vera
Schulz, Axel R
Mateos, Angelo
Holm, Liisa
Pettersson, Ralf F
Vaheri, Antti
Flick, Ramon
Plyusnin, Alexander
Oligomerization of Uukuniemi virus nucleocapsid protein
title Oligomerization of Uukuniemi virus nucleocapsid protein
title_full Oligomerization of Uukuniemi virus nucleocapsid protein
title_fullStr Oligomerization of Uukuniemi virus nucleocapsid protein
title_full_unstemmed Oligomerization of Uukuniemi virus nucleocapsid protein
title_short Oligomerization of Uukuniemi virus nucleocapsid protein
title_sort oligomerization of uukuniemi virus nucleocapsid protein
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2925374/
https://www.ncbi.nlm.nih.gov/pubmed/20698970
http://dx.doi.org/10.1186/1743-422X-7-187
work_keys_str_mv AT katzanna oligomerizationofuukuniemivirusnucleocapsidprotein
AT freibergalexandern oligomerizationofuukuniemivirusnucleocapsidprotein
AT backstromvera oligomerizationofuukuniemivirusnucleocapsidprotein
AT schulzaxelr oligomerizationofuukuniemivirusnucleocapsidprotein
AT mateosangelo oligomerizationofuukuniemivirusnucleocapsidprotein
AT holmliisa oligomerizationofuukuniemivirusnucleocapsidprotein
AT petterssonralff oligomerizationofuukuniemivirusnucleocapsidprotein
AT vaheriantti oligomerizationofuukuniemivirusnucleocapsidprotein
AT flickramon oligomerizationofuukuniemivirusnucleocapsidprotein
AT plyusninalexander oligomerizationofuukuniemivirusnucleocapsidprotein