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dc.contributor.authorTan, Yee-Joo
dc.contributor.authorFielding, Burtram C.
dc.contributor.authorGoh, Phuay-Yee
dc.contributor.authorShen, Shuo
dc.contributor.authorTan, Timothy H.P.
dc.contributor.authorLim, Seng Gee
dc.contributor.authorHong, Wanjin
dc.date.accessioned2014-01-07T19:36:25Z
dc.date.available2014-01-07T19:36:25Z
dc.date.issued2004
dc.identifier.citationTan, Y., et al. (2004). Overexpression of 7a, a Protein Specifically Encoded by the Severe Acute Respiratory Syndrome Coronavirus, Induces Apoptosis via a Caspase-Dependent Pathway. Journal of Virology, 78(24): 14043–14047en_US
dc.identifier.issn0022-538X
dc.identifier.urihttp://hdl.handle.net/10566/917
dc.description.abstractBesides 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.en_US
dc.language.isoenen_US
dc.publisherAmerican Society for Microbiologyen_US
dc.rightsCopyright American Society for Microbiology. This file may be freely used for educational purposes, as long as it is not altered in any way. Acknowledgement of the authors and the source is required.
dc.source.urihttp://dx.doi.org/10.1128/JVI.78.24.14043-14047.2004
dc.titleOverexpression of 7a, a Protein Specifically Encoded by the Severe Acute Respiratory Syndrome Coronavirus, Induces Apoptosis via a Caspase-Dependent Pathwayen_US
dc.typeArticleen_US
dc.privacy.showsubmitterfalse
dc.status.ispeerreviewedtrue
dc.description.accreditationWeb of Scienceen_US


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