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PMID: 273902 Published · ppublish English Journal Article Research Support, U.S. Gov't, Non-P.H.S. Research Support, U.S. Gov't, P.H.S.

Preparation and template activities of polynucleotides containing O2- and O4-alkyluridine.

Singer B, Fraenkel-Conrat H, Kuśmierek JT

Abstract

O2-Ethyl-UDP and O4-methyl-UDP have been prepared and copolymerized in various proportions with UDP or CDP, using polynucleotide phosphorylase. The copolymers were used as templates for DNA-dependent RNA polymerases in the presence of Mn2+. Both of the O-alkylated uridines caused a similar misincorporations. When copolymerized with U they led to incorporation of CMP and GMP into the poly(A). No AMP or UMP incorporation seemed to be caused by the introduction of O-alkyluridines into either poly(U) or poly(C). The mispairing of O2- and O4-alkyluridine to behave like C or G represents mutagenic events. O2 alkylation of U or T is, in contrast to O4 alkylation, a relatively frequent result of treatment of double-stranded nucleic acids with N-nitroso alkylating agents. In single-stranded nucleic acids both O2 and O4 alkylations of U and T occur to similar extents. Thus, the observed mutagenic effects of O2 and O4 alkylation of U may be involved in the high carcinogenicity of these alkylating agents.

MeSH Terms
Alkylation DNA-Directed RNA Polymerases/metabolism Mutation Polyribonucleotides/chemical synthesis,metabolism Structure-Activity Relationship Templates, Genetic Uridine/analogs & derivatives
Chemicals
Polyribonucleotides DNA-Directed RNA Polymerases Uridine
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Singer B
Fraenkel-Conrat H
Kuśmierek J T
References (24)
24 references, click to expand
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Article Info
Journal
Proceedings of the National Academy of Sciences of the United States of America
Abbr.
Proc Natl Acad Sci U S A
ISSN
0027-8424
Published
1978-04-00
Pages
1722-6
Language
English
Region
United States
NLM ID
7505876
PMCID
PMC392411
Subset
IM
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