Literature DB >> 15564512

Overexpression of 7a, a protein specifically encoded by the severe acute respiratory syndrome coronavirus, induces apoptosis via a caspase-dependent pathway.

Yee-Joo Tan1, Burtram C Fielding, Phuay-Yee Goh, Shuo Shen, Timothy H P Tan, Seng Gee Lim, Wanjin Hong.   

Abstract

Besides genes that are homologous to proteins found in other coronaviruses, the severe acute respiratory syndrome coronavirus genome also contains nine other potential open reading frames. Previously, we have characterized the expression and cellular localization of two of these "accessory" viral proteins, 3a (previously termed U274) and 7a (previously termed U122). In this study, we further examined whether they can induce apoptosis, which has been observed clinically. We showed that the overexpression of 7a, but not of 3a or the viral structural proteins, nucleocapsid, membrane, and envelope, induces apoptosis. 7a induces apoptosis via a caspase-dependent pathway and in cell lines derived from different organs, including lung, kidney, and liver.

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Year:  2004        PMID: 15564512      PMCID: PMC533950          DOI: 10.1128/JVI.78.24.14043-14047.2004

Source DB:  PubMed          Journal:  J Virol        ISSN: 0022-538X            Impact factor:   5.103


  32 in total

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Journal:  N Engl J Med       Date:  2003-04-10       Impact factor: 91.245

4.  In vitro detection of apoptosis in monocytes/macrophages infected with human coronavirus.

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Journal:  Clin Diagn Lab Immunol       Date:  2002-11

Review 5.  Host defense, viruses and apoptosis.

Authors:  G N Barber
Journal:  Cell Death Differ       Date:  2001-02       Impact factor: 15.828

6.  Induction of caspase-dependent apoptosis in cultured cells by the avian coronavirus infectious bronchitis virus.

Authors:  C Liu; H Y Xu; D X Liu
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Review 7.  New EMBO members' review: viral and bacterial proteins regulating apoptosis at the mitochondrial level.

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  100 in total

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5.  Nuclear magnetic resonance structure of the N-terminal domain of nonstructural protein 3 from the severe acute respiratory syndrome coronavirus.

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6.  A Kinome-Wide Small Interfering RNA Screen Identifies Proviral and Antiviral Host Factors in Severe Acute Respiratory Syndrome Coronavirus Replication, Including Double-Stranded RNA-Activated Protein Kinase and Early Secretory Pathway Proteins.

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7.  Severe acute respiratory syndrome coronavirus infection of human ciliated airway epithelia: role of ciliated cells in viral spread in the conducting airways of the lungs.

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9.  The hepatitis C virus core protein contains a BH3 domain that regulates apoptosis through specific interaction with human Mcl-1.

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10.  Reverse genetic characterization of the natural genomic deletion in SARS-Coronavirus strain Frankfurt-1 open reading frame 7b reveals an attenuating function of the 7b protein in-vitro and in-vivo.

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