The severe acute respiratory syndrome coronavirus 3a is a novel structural protein
Identifieur interne : 000E51 ( Ncbi/Curation ); précédent : 000E50; suivant : 000E52The severe acute respiratory syndrome coronavirus 3a is a novel structural protein
Auteurs : Shuo Shen [Singapour] ; Pi-Shiu Lin [République populaire de Chine] ; Yu-Chan Chao [République populaire de Chine] ; Aihua Zhang [République populaire de Chine] ; Xiaoming Yang [République populaire de Chine] ; Seng Gee Lim [Singapour] ; Wanjin Hong [Singapour] ; Yee-Joo Tan [Singapour]Source :
- Biochemical and Biophysical Research Communications [ 0006-291X ] ; 2005.
Descripteurs français
- KwdFr :
- MESH :
English descriptors
- KwdEn :
- MESH :
- chemical , chemistry : Viral Proteins, Viral Structural Proteins.
- chemical , metabolism : Viral Proteins, Viral Structural Proteins.
- chemical : DNA, Complementary.
- genetics : Baculoviridae.
- Animals, Chlorocebus aethiops, Open Reading Frames, Plasmids, Recombination, Genetic, Vero Cells.
Abstract
The severe acute respiratory syndrome coronavirus (SARS-CoV) 3a protein is one of the opening reading frames in the viral genome with no homologue in other known coronaviruses. Expression of the 3a protein has been demonstrated during both in vitro and in vivo infection. Here we present biochemical data to show that 3a is a novel coronavirus structural protein. 3a was detected in virions purified from SARS-CoV infected Vero E6 cells although two truncated products were present predominantly instead of the full-length protein. In Vero E6 cells transiently transfected with a cDNA construct for expressing 3a, a similar cleavage was observed. Furthermore, co-expression of 3a, membrane and envelope proteins using the baculovirus system showed that both full-length and truncated 3a can be assembled into virus-like particles. This is the first report that demonstrated the incorporation of 3a into virion and showed that the SARS-CoV encodes a novel coronavirus structural protein.
Url:
DOI: 10.1016/j.bbrc.2005.02.153
PubMed: 15781262
PubMed Central: 7092867
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PMC:7092867Le document en format XML
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<front><div type="abstract" xml:lang="en"><p>The severe acute respiratory syndrome coronavirus (SARS-CoV) 3a protein is one of the opening reading frames in the viral genome with no homologue in other known coronaviruses. Expression of the 3a protein has been demonstrated during both in vitro and in vivo infection. Here we present biochemical data to show that 3a is a novel coronavirus structural protein. 3a was detected in virions purified from SARS-CoV infected Vero E6 cells although two truncated products were present predominantly instead of the full-length protein. In Vero E6 cells transiently transfected with a cDNA construct for expressing 3a, a similar cleavage was observed. Furthermore, co-expression of 3a, membrane and envelope proteins using the baculovirus system showed that both full-length and truncated 3a can be assembled into virus-like particles. This is the first report that demonstrated the incorporation of 3a into virion and showed that the SARS-CoV encodes a novel coronavirus structural protein.</p>
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