Active genes are tri-methylated at K4 of histone H3


Santos-Rosa H., Schneider R., Bannister A. J., Sherriff J., Bernstein B. E., EMRE N. C. T., ...Daha Fazla

Nature, cilt.419, sa.6905, ss.407-411, 2002 (SCI-Expanded, Scopus)

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 419 Sayı: 6905
  • Basım Tarihi: 2002
  • Doi Numarası: 10.1038/nature01080
  • Dergi Adı: Nature
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Sayfa Sayıları: ss.407-411
  • Boğaziçi Üniversitesi Adresli: Hayır

Özet

Lysine methylation of histones in vivo occurs in three states: mono-, di- and tri-methyl. Histone H3 has been found to be dimethylated at lysine 4 (K4) in active euchromatic regions but not in silent heterochromatic sites. Here we show that the Saccharomyces cerevisiae Set1 protein can catalyse di- and tri-methylation of K4 and stimulate the activity of many genes. Using antibodies that discriminate between the di- and tri-methylated state of K4 we show that di-methylation occurs at both inactive and active euchromatic genes, whereas tri-methylation is present exclusively at active genes. It is therefore the presence of a trimethylated K4 that defines an active state of gene expression. These findings establish the concept of methyl status as a determinant for gene activity and thus extend considerably the complexity of histone modifications.