Cloning and characterization of the genes encoding the Mspl restriction modification system

P. M. Lin, Chao-Hung Lee, R. J. Robert

Research output: Contribution to journalArticle

47 Citations (Scopus)

Abstract

The genes encoding the Mspl restriction modification system, which recognizes the sequence 5′CCGG, have been cloned into pUC9. Selection was based on expression of the cloned methylase gene which renders plasmid DNA insensitive to Mspl cleavage in vitro. Initially, an insert of 15kb was obtained which, upon subcloning, yielded a 3 kb EcoRI to HindIII insert, carrying the genes for both the methylase and the restriction enzyme. This insert has been sequenced. Based upon the sequence, together with appropriate subclones, it is shown that the two genes are transcribed divergently with the methylase gene encoding a polypeptide of 418 amino acids, while the restriction enzyme is composed of 262 amino acids. Comparison of the sequence of the Mspl methylase with other cytosine methylases shows a striking degree of similarity. Especially noteworthy is the high degree of similarity with the HhaI and EcoRII methylases.

Original languageEnglish (US)
Pages (from-to)3001-3011
Number of pages11
JournalNucleic Acids Research
Volume17
Issue number8
DOIs
StatePublished - Apr 25 1989
Externally publishedYes

Fingerprint

DNA Restriction-Modification Enzymes
Gene encoding
Cloning
Organism Cloning
Encoding
Genes
Restriction
Gene
Amino acids
Enzymes
Amino Acids
Cytosine
Polypeptides
Plasmids
DNA
Peptides

ASJC Scopus subject areas

  • Statistics, Probability and Uncertainty
  • Applied Mathematics
  • Health, Toxicology and Mutagenesis
  • Toxicology
  • Genetics(clinical)
  • Genetics

Cite this

Cloning and characterization of the genes encoding the Mspl restriction modification system. / Lin, P. M.; Lee, Chao-Hung; Robert, R. J.

In: Nucleic Acids Research, Vol. 17, No. 8, 25.04.1989, p. 3001-3011.

Research output: Contribution to journalArticle

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