Please use this identifier to cite or link to this item: http://hdl.handle.net/2381/23999
Title: Temperature-sensitive mutants in the vaccinia virus A18R gene increase double-stranded RNA synthesis as a result of aberrant viral transcription.
Authors: Bayliss, CD
Condit, RC
First Published: May-1993
Citation: VIROLOGY, 1993, 194 (1), pp. 254-262
Abstract: Mutations in the vaccinia gene A18R cause activation of the cellular ribonucleolytic 2-5A pathway. To determine the mechanism of 2-5A pathway activation, mutant infections were analyzed for synthesis of double-stranded RNA and for transcription of individual virus genes. At late times postinfection, A18R mutant-infected cells contained an increased amount of complementary RNA and a higher steady state level of RNA from regions of the genome transcribed normally only early in the infection. The phenotype of A18R ts mutants is indistinguishable from that of wild-type infections done in the presence of isatin-beta-thiosemicarbazone (IBT). Actinomycin D is a potent inhibitor of activation of the 2-5A pathway in IBT-treated wt infections. Based on these observations, we conclude that the phenotype induced by A18R mutants or by IBT treatment of wt infections is caused by a loss of control of late viral transcription.
DOI Link: 10.1006/viro.1993.1256
ISSN: 0042-6822
Links: http://hdl.handle.net/2381/23999
Type: Journal Article
Appears in Collections:Published Articles, Dept. of Genetics

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