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PMID: 3036116 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Size of the directing moiety at carbon 5 of cytosine and the activity of human DNA(cytosine-5) methyltransferase.

Biochemical and biophysical research communications ·Vol. 145 ·No. 1 ·1987-05-29 ·Pages 146-52

Hardy TA, Baker DJ, Newman EM, Sowers LC, Goodman MF, Smith SS

Abstract

M13 DNAs in which carbon 5 of each deoxycytidine residue in one strand is replaced with a bulky group are very good substrates for human DNA (cytosine-5) methyltransferase. Rate enhancements of up to 35 fold are obtained depending on the size of the moiety at C-5. The enzyme appears optimally suited to sense a methyl group in one strand at this position. Alkaline density gradient analyses of the distribution of methyl groups applied to 5-BrdCyd or 5-IdCyd substituted DNA reveal that these groups serve to direct the enzyme to methylate the unsubstituted strand.

MeSH Terms
Cytosine/analogs & derivatives DNA (Cytosine-5-)-Methyltransferases/metabolism DNA Restriction Enzymes Humans Kinetics Substrate Specificity
Chemicals
Cytosine DNA (Cytosine-5-)-Methyltransferases DNA Restriction Enzymes
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Hardy T A
Baker D J
Newman E M
Sowers L C
Goodman M F
Smith S S
Article Info
Journal
Biochemical and biophysical research communications
Abbr.
Biochem Biophys Res Commun
ISSN
0006-291X
Published
1987-05-29
Pages
146-52
Language
English
Region
United States
NLM ID
0372516
Subset
IM
Grants
NCI NIH HHS · CA-335172 · United States
NIGMS NIH HHS · GM-21422 · United States
NIGMS NIH HHS · GM-32863 · United States
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