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PMID: 3036132 Published · ppublish English Journal Article

The effects of DNA methylation by Hha I methylase on the cleavage reactions by Hae II, Aha II and Ban I endonucleases.

Biochemical and biophysical research communications ·Vol. 145 ·No. 1 ·1987-05-29 ·Pages 482-7

Kang SC, Choi WS, Yoo OJ

Abstract

The DNA methylated by Hha I methylase was resistant against cleavage of Hae II or Aha II endonuclease indicating that the methyl group of the C5 position of the inmost cytosine nucleotide interferes with the interaction between the enzyme and the hexameric recognition sequence. Considering that Hae II or Aha II methylase has not been isolated yet, the result explained above is a useful information for protecting a double stranded DNA from being cleaved by Hae II or Aha II endonuclease. In contrast to Hae II or Aha II endonuclease, Ban I endonuclease which also has Hha I sequence as its tetrameric core was able to cleave the same DNA normally. This result suggests that the C5 position of the inmost pyrimidine nucleotide is not an important contact point between Ban I endonuclease and its hexameric recognition sequence.

MeSH Terms
DNA (Cytosine-5-)-Methyltransferases/metabolism DNA Restriction Enzymes/metabolism DNA-Cytosine Methylases Deoxyribonucleases, Type II Site-Specific Kinetics Plasmids Substrate Specificity
Chemicals
DNA modification methylase HhaI DNA-Cytosine Methylases DNA (Cytosine-5-)-Methyltransferases DNA Restriction Enzymes endodeoxyribonuclease BanI endodeoxyribonuclease HaeII Deoxyribonucleases, Type II Site-Specific GRCGYC-specific type II deoxyribonucleases
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Kang S C
Choi W S
Yoo O J
Article Info
Journal
Biochemical and biophysical research communications
Abbr.
Biochem Biophys Res Commun
ISSN
0006-291X
Published
1987-05-29
Pages
482-7
Language
English
Region
United States
NLM ID
0372516
Subset
IM
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