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Characterization of a unique group-specific protein (U122) of the severe acute respiratory syndrome coronavirus

Identifieur interne : 005B69 ( Main/Exploration ); précédent : 005B68; suivant : 005B70

Characterization of a unique group-specific protein (U122) of the severe acute respiratory syndrome coronavirus

Auteurs : Burtram C. Fielding [Singapour] ; Yee-Joo Tan [Singapour] ; SHEN SHUO [Singapour] ; Timothy H. P. Tan [Singapour] ; Eng-Eong Ooi [Singapour] ; SENG GEE LIM [Singapour] ; WANJIN HONG [Singapour] ; Phuay-Yee Goh [Singapour]

Source :

RBID : Pascal:04-0392921

Descripteurs français

English descriptors

Abstract

A novel coronavirus (CoV) has been identified as the etiological agent of severe acute respiratory syndrome (SARS). The SARS-CoV genome encodes the characteristic essential CoV replication and structural proteins. Additionally, the genome contains six group-specific open reading frames (ORFs) larger than 50 amino acids, with no known homologues. As with the group-specific genes of the other CoVs, little is known about the SARS-CoV group-specific genes. SARS-CoV ORF7a encodes a putative unique 122-amino-acid protein, designated U122 in this study. The deduced sequence contains a probable cleaved signal sequence and a C-terminal transmembrane helix, indicating that U122 is likely to be a type I membrane protein. The C-terminal tail also contains a typical endoplasmic reticulum (ER) retrieval motif, KRKTE. U122 was expressed in SARS-CoV-infected Vero E6 cells, as it could be detected by Western blot and immunofluorescence analyses. U122 is localized to the perinuclear region of both SARS-CoV-infected and transfected cells and colocalized with ER and intermediate compartment markers. Mutational analyses showed that both the signal peptide sequence and ER retrieval motif were functional.


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Le document en format XML

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<term>Characterization</term>
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<term>Coronavirus</term>
<term>Endoplasmic Reticulum (metabolism)</term>
<term>Humans</term>
<term>Membrane Proteins (chemistry)</term>
<term>Membrane Proteins (genetics)</term>
<term>Membrane Proteins (metabolism)</term>
<term>Microbiology</term>
<term>Molecular Sequence Data</term>
<term>Open Reading Frames (genetics)</term>
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<term>SARS Virus (genetics)</term>
<term>SARS Virus (metabolism)</term>
<term>SARS Virus (pathogenicity)</term>
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<term>Transfection</term>
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<term>Viral Proteins (chemistry)</term>
<term>Viral Proteins (genetics)</term>
<term>Viral Proteins (metabolism)</term>
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<term>Animaux</term>
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<term>Protéines membranaires (génétique)</term>
<term>Protéines membranaires (métabolisme)</term>
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<term>Virus du SRAS (métabolisme)</term>
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<term>Endoplasmic Reticulum</term>
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<term>Viral Proteins</term>
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<term>Protéines membranaires</term>
<term>Protéines virales</term>
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<term>SARS Virus</term>
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<term>Virus du SRAS</term>
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<term>Amino Acid Sequence</term>
<term>Animals</term>
<term>Chlorocebus aethiops</term>
<term>Humans</term>
<term>Molecular Sequence Data</term>
<term>Protein Sorting Signals</term>
<term>Species Specificity</term>
<term>Transfection</term>
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<term>Viral Matrix Proteins</term>
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<term>Animaux</term>
<term>Cellules Vero</term>
<term>Coronavirus</term>
<term>Caractérisation</term>
<term>Données de séquences moléculaires</term>
<term>Humains</term>
<term>Protéine A</term>
<term>Microbiologie</term>
<term>Protéines de la matrice virale</term>
<term>Protéines membranaires</term>
<term>Protéines virales</term>
<term>Signaux de triage des protéines</term>
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<term>Séquence d'acides aminés</term>
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<front>
<div type="abstract" xml:lang="en">A novel coronavirus (CoV) has been identified as the etiological agent of severe acute respiratory syndrome (SARS). The SARS-CoV genome encodes the characteristic essential CoV replication and structural proteins. Additionally, the genome contains six group-specific open reading frames (ORFs) larger than 50 amino acids, with no known homologues. As with the group-specific genes of the other CoVs, little is known about the SARS-CoV group-specific genes. SARS-CoV ORF7a encodes a putative unique 122-amino-acid protein, designated U122 in this study. The deduced sequence contains a probable cleaved signal sequence and a C-terminal transmembrane helix, indicating that U122 is likely to be a type I membrane protein. The C-terminal tail also contains a typical endoplasmic reticulum (ER) retrieval motif, KRKTE. U122 was expressed in SARS-CoV-infected Vero E6 cells, as it could be detected by Western blot and immunofluorescence analyses. U122 is localized to the perinuclear region of both SARS-CoV-infected and transfected cells and colocalized with ER and intermediate compartment markers. Mutational analyses showed that both the signal peptide sequence and ER retrieval motif were functional.</div>
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<name sortKey="Seng Gee Lim" sort="Seng Gee Lim" uniqKey="Seng Gee Lim" last="Seng Gee Lim">SENG GEE LIM</name>
<name sortKey="Seng Gee Lim" sort="Seng Gee Lim" uniqKey="Seng Gee Lim" last="Seng Gee Lim">SENG GEE LIM</name>
<name sortKey="Shen Shuo" sort="Shen Shuo" uniqKey="Shen Shuo" last="Shen Shuo">SHEN SHUO</name>
<name sortKey="Tan, Timothy H P" sort="Tan, Timothy H P" uniqKey="Tan T" first="Timothy H. P." last="Tan">Timothy H. P. Tan</name>
<name sortKey="Tan, Yee Joo" sort="Tan, Yee Joo" uniqKey="Tan Y" first="Yee-Joo" last="Tan">Yee-Joo Tan</name>
<name sortKey="Wanjin Hong" sort="Wanjin Hong" uniqKey="Wanjin Hong" last="Wanjin Hong">WANJIN HONG</name>
</country>
</tree>
</affiliations>
</record>

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