Nucleolar localization of non-structural protein 3b, a protein specifically encoded by the severe acute respiratory syndrome coronavirus

The open reading frame 3 (ORF3) of the severe acute respiratory syndrome coronavirus (SARS-CoV) genome encodes a predicted 154-amino acid protein, which lacks similarities to any known protein, and is named 3b. In this study, it was shown that 3b protein was predominately localized to nucleus with E...

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Published in:Virus research Vol. 114; no. 1; pp. 70 - 79
Main Authors: Yuan, Xiaoling, Yao, Zhenyu, Shan, Yajun, Chen, Bo, Yang, Zhen, Wu, Jie, Zhao, Zhenhu, Chen, Jiapei, Cong, Yuwen
Format: Journal Article
Language:English
Published: Netherlands Elsevier B.V 01-12-2005
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Abstract The open reading frame 3 (ORF3) of the severe acute respiratory syndrome coronavirus (SARS-CoV) genome encodes a predicted 154-amino acid protein, which lacks similarities to any known protein, and is named 3b. In this study, it was shown that 3b protein was predominately localized to nucleus with EGFP tag at its N- or C-terminus. The localization patterns were similar in different transfected cells. Immuno-fluorescence assay revealed that 3b protein was co-localized well with C23 in nucleolus. C23, B23 and fibrillarin all are important nucleolar proteins, which localize in the region of the nucleolus. Co-transfection of p3b-EGFP with pC23-DsRed, pB23-DsRed and pfibrillarin-DsRed further confirmed 3b's nucleolus localization. With construction of serial truncated mutants of 3b, a region (residues 134–154 aa) responsible for nucleolar localization was determinated in 3b protein. These results provide a new insight for further functional studies of SARS-CoV 3b protein.
AbstractList The open reading frame 3 (ORF3) of the severe acute respiratory syndrome coronavirus (SARS-CoV) genome encodes a predicted 154-amino acid protein, which lacks similarities to any known protein, and is named 3b. In this study, it was shown that 3b protein was predominately localized to nucleus with EGFP tag at its N- or C-terminus. The localization patterns were similar in different transfected cells. Immuno-fluorescence assay revealed that 3b protein was co-localized well with C23 in nucleolus. C23, B23 and fibrillarin all are important nucleolar proteins, which localize in the region of the nucleolus. Co-transfection of p3b-EGFP with pC23-DsRed, pB23-DsRed and pfibrillarin-DsRed further confirmed 3b's nucleolus localization. With construction of serial truncated mutants of 3b, a region (residues 134–154 aa) responsible for nucleolar localization was determinated in 3b protein. These results provide a new insight for further functional studies of SARS-CoV 3b protein.
Author Yang, Zhen
Zhao, Zhenhu
Yao, Zhenyu
Wu, Jie
Cong, Yuwen
Shan, Yajun
Yuan, Xiaoling
Chen, Jiapei
Chen, Bo
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  email: congyw@nic.bmi.ac.cn
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Keywords PBS
DMEM
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NLS
SARS-CoV
SARS
EGFP
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ECL
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SSID ssj0006376
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Snippet The open reading frame 3 (ORF3) of the severe acute respiratory syndrome coronavirus (SARS-CoV) genome encodes a predicted 154-amino acid protein, which lacks...
SourceID pubmedcentral
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crossref
pubmed
elsevier
SourceType Open Access Repository
Aggregation Database
Index Database
Publisher
StartPage 70
SubjectTerms Amino Acid Sequence
Animals
Cell Line
Cell Nucleolus - metabolism
Chlorocebus aethiops
Chromosomal Proteins, Non-Histone - metabolism
COS Cells
Green Fluorescent Proteins - genetics
Green Fluorescent Proteins - metabolism
Humans
Nuclear Proteins - metabolism
Nucleolin
Nucleophosmin
Phosphoproteins - metabolism
Protein Sorting Signals
RNA-Binding Proteins - metabolism
SARS coronavirus
Severe acute respiratory syndrome-related coronavirus - genetics
Severe acute respiratory syndrome-related coronavirus - metabolism
Severe acute respiratory syndrome-related coronavirus - pathogenicity
Transfection
Vero Cells
Viral Nonstructural Proteins - chemistry
Viral Nonstructural Proteins - genetics
Viral Nonstructural Proteins - metabolism
Title Nucleolar localization of non-structural protein 3b, a protein specifically encoded by the severe acute respiratory syndrome coronavirus
URI https://dx.doi.org/10.1016/j.virusres.2005.06.001
https://www.ncbi.nlm.nih.gov/pubmed/16046244
https://search.proquest.com/docview/17443862
https://search.proquest.com/docview/68778617
https://pubmed.ncbi.nlm.nih.gov/PMC7114190
Volume 114
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