[24] Enzymatic Methods for Sequence Analysis Applied to DNA Restriction and Methylation Sites

H. O. Smith, Thomas Kelly, P. H. Roy

Research output: Contribution to journalArticle

Abstract

Restriction enzymes are site-specific endonucleases produced by various bacteria, bacterial plasmids, and viruses. In those cases where they produce double-stranded cleavage of DNA within their recognition sites, sequence analysis of the site is equivalent to determination of the 5'- and 3'-terminal bases of the restricted DNA. This chapter describes a method for limited sequencing of the 5' terminus of DNA molecules based on enzymatic cleavage of successively larger oligonucleotides. This procedure was developed especially for analysis of the end sequence of small restriction endonuclease fragments but should be more generally applicable to any small DNA molecule. Every host that produces a restriction endonuclease also produces a companion DNA modification enzyme, usually a methylase, with identical or similar site recognition. This enzyme serves to modify and protect the restriction sites of the host chromosome. The chapter concludes by describing a procedure for partial analysis of methylation sites.

Original languageEnglish (US)
Pages (from-to)282-294
Number of pages13
JournalMethods in Enzymology
Volume29
Issue numberC
DOIs
StatePublished - Jan 1 1974
Externally publishedYes

Fingerprint

Methylation
DNA Methylation
Sequence Analysis
DNA
DNA Restriction Enzymes
Enzymes
Molecules
Endonucleases
Chromosomes
Viruses
Oligonucleotides
Bacteria
Plasmids

ASJC Scopus subject areas

  • Biochemistry
  • Molecular Biology

Cite this

[24] Enzymatic Methods for Sequence Analysis Applied to DNA Restriction and Methylation Sites. / Smith, H. O.; Kelly, Thomas; Roy, P. H.

In: Methods in Enzymology, Vol. 29, No. C, 01.01.1974, p. 282-294.

Research output: Contribution to journalArticle

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