SrasV1, PubMed, Checkpoint, bibRecord, 002599

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

Identifieur interne : 002599 ( PubMed/Checkpoint ); précédent : 002598; suivant : 002600

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

Auteurs : Xiaoling Yuan [République populaire de Chine] ; Zhenyu Yao ; Yajun Shan ; Bo Chen ; Zhen Yang ; Jie Wu ; Zhenhu Zhao ; Jiapei Chen ; Yuwen Cong

Source :

Virus research [ 0168-1702 ] ; 2005.

RBID : pubmed:16046244

Descripteurs français

English descriptors

KwdEn :
- Amino Acid Sequence, Animals, COS Cells, Cell Line, Cell Nucleolus (metabolism), Chlorocebus aethiops, Chromosomal Proteins, Non-Histone (metabolism), Green Fluorescent Proteins (genetics), Green Fluorescent Proteins (metabolism), Humans, Nuclear Proteins (metabolism), Phosphoproteins (metabolism), Protein Sorting Signals, RNA-Binding Proteins (metabolism), SARS Virus (genetics), SARS Virus (metabolism), SARS Virus (pathogenicity), Transfection, Vero Cells, Viral Nonstructural Proteins (chemistry), Viral Nonstructural Proteins (genetics), Viral Nonstructural Proteins (metabolism).
MESH :
- chemical , chemistry : Viral Nonstructural Proteins.
- chemical , genetics : Green Fluorescent Proteins, Viral Nonstructural Proteins.
- chemical , metabolism : Chromosomal Proteins, Non-Histone, Green Fluorescent Proteins, Nuclear Proteins, Phosphoproteins, RNA-Binding Proteins, Viral Nonstructural Proteins.
- genetics : SARS Virus.
- metabolism : Cell Nucleolus, SARS Virus.
- pathogenicity : SARS Virus.
- Amino Acid Sequence, Animals, COS Cells, Cell Line, Chlorocebus aethiops, Humans, Protein Sorting Signals, Transfection, Vero Cells.

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.

DOI: 10.1016/j.virusres.2005.06.001
PubMed: 16046244

Affiliations:

Links toward previous steps (curation, corpus...)

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pubmed:16046244

Le document en format XML

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<front><div type="abstract" xml:lang="en">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.</div>
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<Abstract><AbstractText>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.</AbstractText>
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Nucleolar localization of non-structural protein 3b, a protein specifically encoded by the severe acute respiratory syndrome coronavirus.

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

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