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Small interfering RNA inhibits SARS-CoV nucleocapsid gene expression in cultured cells and mouse muscles.

Identifieur interne : 000F14 ( Ncbi/Checkpoint ); précédent : 000F13; suivant : 000F15

Small interfering RNA inhibits SARS-CoV nucleocapsid gene expression in cultured cells and mouse muscles.

Auteurs : Ping Zhao [République populaire de Chine] ; Zhao-Ling Qin ; Jin-Shan Ke ; Yang Lu ; Min Liu ; Wei Pan ; Lan-Juan Zhao ; Jie Cao ; Zhong-Tian Qi

Source :

RBID : pubmed:15848179

Descripteurs français

English descriptors

Abstract

SARS-CoV is a newly identified coronavirus that causes severe acute respiratory syndrome (SARS). Currently, there is no effective method available for prophylaxis and treatment of SARS-CoV infections. In the present study, the influence of small interfering RNA (siRNA) on SARS-CoV nucleocapsid (N) protein expression was detected in cultured cells and mouse muscles. Four siRNA expression cassettes driven by mouse U6 promoter targeting SARS-CoV N gene were prepared, and their inhibitory effects on expression of N and enhanced green fluorescence protein (EGFP) fusion protein were observed. A candidate siRNA was proved to down-regulate N and EGFP expression actively in a sequence-specific manner. The expression vector of this siRNA was constructed and confirmed to reduce N and EGFP expression efficiently in both cultured cells and adult mouse muscles. Our findings suggest that the siRNA should provide the basis for prophylaxis and therapy of SARS-CoV infection in human.

DOI: 10.1016/j.febslet.2005.02.080
PubMed: 15848179


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pubmed:15848179

Le document en format XML

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<nlm:affiliation>Department of Microbiology, Second Military Medical University, Shanghai, China.</nlm:affiliation>
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<name sortKey="Ke, Jin Shan" sort="Ke, Jin Shan" uniqKey="Ke J" first="Jin-Shan" last="Ke">Jin-Shan Ke</name>
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<name sortKey="Lu, Yang" sort="Lu, Yang" uniqKey="Lu Y" first="Yang" last="Lu">Yang Lu</name>
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<name sortKey="Liu, Min" sort="Liu, Min" uniqKey="Liu M" first="Min" last="Liu">Min Liu</name>
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<name sortKey="Pan, Wei" sort="Pan, Wei" uniqKey="Pan W" first="Wei" last="Pan">Wei Pan</name>
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<name sortKey="Zhao, Lan Juan" sort="Zhao, Lan Juan" uniqKey="Zhao L" first="Lan-Juan" last="Zhao">Lan-Juan Zhao</name>
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<name sortKey="Cao, Jie" sort="Cao, Jie" uniqKey="Cao J" first="Jie" last="Cao">Jie Cao</name>
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<name sortKey="Ke, Jin Shan" sort="Ke, Jin Shan" uniqKey="Ke J" first="Jin-Shan" last="Ke">Jin-Shan Ke</name>
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<name sortKey="Lu, Yang" sort="Lu, Yang" uniqKey="Lu Y" first="Yang" last="Lu">Yang Lu</name>
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<name sortKey="Liu, Min" sort="Liu, Min" uniqKey="Liu M" first="Min" last="Liu">Min Liu</name>
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<name sortKey="Pan, Wei" sort="Pan, Wei" uniqKey="Pan W" first="Wei" last="Pan">Wei Pan</name>
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<name sortKey="Zhao, Lan Juan" sort="Zhao, Lan Juan" uniqKey="Zhao L" first="Lan-Juan" last="Zhao">Lan-Juan Zhao</name>
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<name sortKey="Cao, Jie" sort="Cao, Jie" uniqKey="Cao J" first="Jie" last="Cao">Jie Cao</name>
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<name sortKey="Qi, Zhong Tian" sort="Qi, Zhong Tian" uniqKey="Qi Z" first="Zhong-Tian" last="Qi">Zhong-Tian Qi</name>
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<term>Gene Expression (genetics)</term>
<term>Genetic Vectors (genetics)</term>
<term>Green Fluorescent Proteins (genetics)</term>
<term>Green Fluorescent Proteins (metabolism)</term>
<term>Humans</term>
<term>Mice</term>
<term>Muscles (metabolism)</term>
<term>Nucleocapsid Proteins (genetics)</term>
<term>Nucleocapsid Proteins (metabolism)</term>
<term>Promoter Regions, Genetic (genetics)</term>
<term>RNA, Small Interfering (genetics)</term>
<term>RNA, Small Interfering (metabolism)</term>
<term>RNA, Small Nuclear (genetics)</term>
<term>Recombinant Proteins (genetics)</term>
<term>Recombinant Proteins (metabolism)</term>
<term>SARS Virus (genetics)</term>
<term>SARS Virus (metabolism)</term>
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<term>Animaux</term>
<term>Cricetinae</term>
<term>Expression des gènes (génétique)</term>
<term>Humains</term>
<term>Lignée cellulaire</term>
<term>Muscles (métabolisme)</term>
<term>Petit ARN interférent (génétique)</term>
<term>Petit ARN interférent (métabolisme)</term>
<term>Petit ARN nucléaire (génétique)</term>
<term>Protéines nucléocapside (génétique)</term>
<term>Protéines nucléocapside (métabolisme)</term>
<term>Protéines recombinantes (génétique)</term>
<term>Protéines recombinantes (métabolisme)</term>
<term>Protéines à fluorescence verte (génétique)</term>
<term>Protéines à fluorescence verte (métabolisme)</term>
<term>Régions promotrices (génétique) (génétique)</term>
<term>Souris</term>
<term>Vecteurs génétiques (génétique)</term>
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<term>Gene Expression</term>
<term>Genetic Vectors</term>
<term>Promoter Regions, Genetic</term>
<term>SARS Virus</term>
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<term>Expression des gènes</term>
<term>Petit ARN interférent</term>
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<term>Protéines nucléocapside</term>
<term>Protéines recombinantes</term>
<term>Protéines à fluorescence verte</term>
<term>Régions promotrices (génétique)</term>
<term>Vecteurs génétiques</term>
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<term>RNA, Small Interfering</term>
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<term>Petit ARN interférent</term>
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<front>
<div type="abstract" xml:lang="en">SARS-CoV is a newly identified coronavirus that causes severe acute respiratory syndrome (SARS). Currently, there is no effective method available for prophylaxis and treatment of SARS-CoV infections. In the present study, the influence of small interfering RNA (siRNA) on SARS-CoV nucleocapsid (N) protein expression was detected in cultured cells and mouse muscles. Four siRNA expression cassettes driven by mouse U6 promoter targeting SARS-CoV N gene were prepared, and their inhibitory effects on expression of N and enhanced green fluorescence protein (EGFP) fusion protein were observed. A candidate siRNA was proved to down-regulate N and EGFP expression actively in a sequence-specific manner. The expression vector of this siRNA was constructed and confirmed to reduce N and EGFP expression efficiently in both cultured cells and adult mouse muscles. Our findings suggest that the siRNA should provide the basis for prophylaxis and therapy of SARS-CoV infection in human.</div>
</front>
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