Literature DB >> 1736538

Yeast killer virus transcription initiation in vitro.

F P Barbone1, T L Williams, M J Leibowitz.   

Abstract

Killer virions isolated from infected Saccharomyces cerevisiae cells contain an RNA polymerase activity which catalyzes the transcription in vitro of positive polarity RNAs from the L-A and M double-stranded RNA genomic segments of the virus. The RNA polymerase can initiate transcription in vitro with gamma-thio-GTP, whose thiophosphate group is found on the 5' terminus of transcripts. Transcripts produced in vitro by the virion-associated RNA polymerase in the presence of 7mGpppG are significantly more active as translational templates than are transcripts produced in its absence. However, unlike Escherichia coli RNA polymerase transcripts from viral cDNA made in the presence of 7mGpppG, transcripts produced by viral RNA polymerase in the presence of 7mGpppG fail to bind to antibody against 7mG.

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Year:  1992        PMID: 1736538     DOI: 10.1016/0042-6822(92)90323-h

Source DB:  PubMed          Journal:  Virology        ISSN: 0042-6822            Impact factor:   3.616


  3 in total

1.  Yeast double-stranded RNA virus L-A deliberately synthesizes RNA transcripts with 5'-diphosphate.

Authors:  Tsutomu Fujimura; Rosa Esteban
Journal:  J Biol Chem       Date:  2010-05-28       Impact factor: 5.157

2.  Kinetic studies of killer toxin K1 binding to yeast cells indicate two receptor populations.

Authors:  H Kurzweilová; K Sigler
Journal:  Arch Microbiol       Date:  1994       Impact factor: 2.552

3.  His-154 is involved in the linkage of the Saccharomyces cerevisiae L-A double-stranded RNA virus Gag protein to the cap structure of mRNAs and is essential for M1 satellite virus expression.

Authors:  A Blanc; J C Ribas; R B Wickner; N Sonenberg
Journal:  Mol Cell Biol       Date:  1994-04       Impact factor: 4.272

  3 in total

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