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PMID: 3178838 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

RNA mediated formation of a phosphorothioate diester bond.

Biochemical and biophysical research communications ·Vol. 156 ·No. 1 ·1988-10-14 ·Pages 340-7

Buzayan JM, Feldstein PA, Bruening G, Eckstein F

Abstract

Previous results showed that multimeric, tandemly sequence-repeated forms of satellite tobacco ringspot virus RNA of the encapsidated polarity (STobRV (+)RNA) autolytically process at a specific phosphodiester bond, the junction. Substituting a phosphorothioate diester bond for the STobRV (+)RNA junction drastically slowed autolytic processing. Here we show that for the complementary STobRV (-)RNA, in contrast, replacing sets of phosphodiester bonds with phosphorothioate diester bonds, even at the junction, did not greatly slow autolytic processing or spontaneous ligation, the usual reactions of the unmodified RNA. In the ligation reaction STobRV (-)RNA directed the formation of an ApG phosphorothioate diester bond.

MeSH Terms
Base Sequence DNA-Directed RNA Polymerases/metabolism Kinetics Plant Viruses/genetics,metabolism Plasmids RNA, Viral/genetics,metabolism Thionucleotides/metabolism Transcription, Genetic
Chemicals
RNA, Viral Thionucleotides DNA-Directed RNA Polymerases
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Buzayan J M
Department of Plant Pathology, College of Agricultural and Environmental Sciences, University of California, Davis 95616.
Feldstein P A
Bruening G
Eckstein F
Article Info
Journal
Biochemical and biophysical research communications
Abbr.
Biochem Biophys Res Commun
ISSN
0006-291X
Published
1988-10-14
Pages
340-7
Language
English
Region
United States
NLM ID
0372516
Subset
IM
Grants
NIGMS NIH HHS · GM37627 · United States
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