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PMID: 6262303 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

DNA is linked to the rat liver DNA nicking-closing enzyme by a phosphodiester bond to tyrosine.

The Journal of biological chemistry ·Vol. 256 ·No. 10 ·1981-05-25 ·Pages 4805-9

Champoux JJ

Abstract

Conditions which result in DNA strand breakage by the rat liver DNA nicking-closing enzyme lead to the covalent attachment of the 3'-end of the broken strand to the enzyme. Treatment of this complex with pancreatic DNase leaves a residue of 17 +/- 8 nucleotide phosphates still attached to the enzyme. Subsequent nuclease P1 treatment removes all but 2 +/- 1 phosphate residues. Using nuclease P1-treated complexes which had been labeled in the DNA with 32P, the stability of the protein-DNA linkage was studied. The linkage is stable to acid, base, neutral and acidic hydroxylamine, and neutral I2. This pattern of stability rules out essentially all of the possible DNA-protein linkages except for a linkage involving a phosphodiester bond to the amino acid tyrosine. After acid hydrolysis of the 32P-labeled complexes, label was found to be associated with O4-phosphotyrosine, providing a direct demonstration that tyrosine is the amino acid to which the end of the DNA chain is attached.

MeSH Terms
Animals Bacteriophage phi X 174 DNA Topoisomerases, Type I/metabolism DNA, Viral/metabolism Kinetics Liver/enzymology Organophosphates Protein Binding Rats Simian virus 40 Tyrosine
Chemicals
DNA, Viral Organophosphates Tyrosine DNA Topoisomerases, Type I
Authors & Affiliations
1 authors, click to expand affiliations / ORCID
Champoux J J
Article Info
Journal
The Journal of biological chemistry
Abbr.
J Biol Chem
ISSN
0021-9258
Published
1981-05-25
Pages
4805-9
Language
English
Region
United States
NLM ID
2985121R
Subset
IM
Grants
NIGMS NIH HHS · GM23224 · United States
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