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PMID: 2476230 Published · ppublish English Journal Article Review

Avoidance of DNA methylation. A virus-encoded methylase inhibitor and evidence for counterselection of methylase recognition sites in viral genomes.

Cell biophysics ·Vol. 15 ·No. 1-2 ·1989-00-00 ·Pages 87-95

Krüger DH, Schroeder C, Santibanez-Koref M, Reuter M

Abstract

The ocr+ gene of bacterial virus T7 codes for the first protein recognized to inhibit a specific group of DNA methylases. The recognition sequences of several other DNA methylases, not susceptible to Ocr inhibition, are significantly suppressed in the virus genome. The bacterial virus T3 encodes an Ado-Met hydrolase, destroying the methyl donor and causing T3 DNA to be totally unmethylated. These observations could stimulate analogous investigations into the regulation of DNA methylation patterns of eukaryotic viruses and cells. For instance, an underrepresentation of methylation sites (5'-CG) is also true for animal DNA viruses. Moreover, we were able to disclose some novel properties of DNA restriction-modification enzymes concerning the protection of DNA recognition sequences in which only one strand can be methylated (e.g., type III enzyme EcoP15) and the primary resistance of (unmethylated) DNA recognition sites towards type II restriction endonuclease EcoRII.

MeSH Terms
Base Sequence DNA Modification Methylases/antagonists & inhibitors,metabolism DNA, Viral/metabolism Genes, Viral Hydrolases/genetics,metabolism Methylation T-Phages/enzymology,genetics,metabolism
Chemicals
DNA, Viral DNA Modification Methylases Hydrolases adenosylmethionine hydrolase
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Krüger D H
Institute of Medical Virology, Humboldt University School of Medicine, Charité, Berlin, German Democratic Republic.
Schroeder C
Santibanez-Koref M
Reuter M
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Article Info
Journal
Cell biophysics
Abbr.
Cell Biophys
ISSN
0163-4992
Published
1989-00-00
Pages
87-95
Language
English
Region
United States
NLM ID
8002185
Subset
IM
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