Wheat endonuclease WEN1 dependent on S-adenosyl-L-methionine and sensitive to DNA methylation status

Epigenetics. 2007 Jan-Mar;2(1):50-3. doi: 10.4161/epi.2.1.3933. Epub 2007 Feb 1.

Abstract

Ca(2+)-, Mg(2+)-dependent wheat endonuclease WEN1 with molecular mass of about 27 kDa was isolated from coleoptyles. Methylated DNA of lambda phage grown on E. coli dam(+), dcm(+) cells was hydrolyzed by WEN1 more effectively than DNA of phage grown on dam(-), dcm(-) cells. Two pH activity maxima (pH 6.5-7.5 and 9.0-10.5) were observed when double-stranded DNA was hydrolyzed. WEN1 is stable at elevated temperatures (65 degrees C ) and in wide range of pH values. WEN1 is activated by S-adenosyl-L-methionine, S-adenosyl-L-homocysteine and S-isobutyladenosine. It is a first case to show that higher eukaryote endonuclease discriminates between DNA of various methylation status and is modulated by S-AdoMet and its analogs.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cations, Divalent / pharmacology
  • DNA Methylation*
  • DNA, Plant / genetics*
  • Endodeoxyribonucleases / isolation & purification
  • Endodeoxyribonucleases / metabolism*
  • Plant Proteins / isolation & purification
  • Plant Proteins / metabolism*
  • S-Adenosylmethionine / metabolism*
  • Seedlings / enzymology
  • Triticum / enzymology*
  • Triticum / genetics*

Substances

  • Cations, Divalent
  • DNA, Plant
  • Plant Proteins
  • S-Adenosylmethionine
  • Endodeoxyribonucleases
  • calcium magnesium dependent endodeoxyribonuclease