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PR Domain-containing Protein 7 (PRDM7) Is a Histone 3 Lysine 4 Trimethyltransferase.
Blazer, Levi L; Lima-Fernandes, Evelyne; Gibson, Elisa; Eram, Mohammad S; Loppnau, Peter; Arrowsmith, Cheryl H; Schapira, Matthieu; Vedadi, Masoud.
Afiliação
  • Blazer LL; From the Structural Genomics Consortium, University of Toronto, Toronto, Ontario M5G 1L7.
  • Lima-Fernandes E; From the Structural Genomics Consortium, University of Toronto, Toronto, Ontario M5G 1L7.
  • Gibson E; From the Structural Genomics Consortium, University of Toronto, Toronto, Ontario M5G 1L7.
  • Eram MS; From the Structural Genomics Consortium, University of Toronto, Toronto, Ontario M5G 1L7.
  • Loppnau P; From the Structural Genomics Consortium, University of Toronto, Toronto, Ontario M5G 1L7.
  • Arrowsmith CH; From the Structural Genomics Consortium, University of Toronto, Toronto, Ontario M5G 1L7, the Princess Margaret Cancer Centre and Department of Medical Biophysics, University of Toronto, Toronto, Ontario M5G 2M9, and.
  • Schapira M; From the Structural Genomics Consortium, University of Toronto, Toronto, Ontario M5G 1L7, the Department of Pharmacology and Toxicology, University of Toronto, Toronto, Ontario M5S 1A8, Canada.
  • Vedadi M; From the Structural Genomics Consortium, University of Toronto, Toronto, Ontario M5G 1L7, the Department of Pharmacology and Toxicology, University of Toronto, Toronto, Ontario M5S 1A8, Canada m.vedadi@utoronto.ca.
J Biol Chem ; 291(26): 13509-19, 2016 Jun 24.
Article em En | MEDLINE | ID: mdl-27129774
PR domain-containing protein 7 (PRDM7) is a primate-specific histone methyltransferase that is the result of a recent gene duplication of PRDM9. The two proteins are highly homologous, especially in the catalytic PR/SET domain, where they differ by only three amino acid residues. Here we report that PRDM7 is an efficient methyltransferase that selectively catalyzes the trimethylation of H3 lysine 4 (H3K4) both in vitro and in cells. Through selective mutagenesis we have dissected the functional roles of each of the three divergent residues between the PR domains of PRDM7 and PRDM9. These studies indicate that after a single serine to tyrosine mutation at residue 357 (S357Y), PRDM7 regains the substrate specificities and catalytic activities similar to its evolutionary predecessor, including the ability to efficiently methylate H3K36.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Histona-Lisina N-Metiltransferase Limite: Humans Idioma: En Revista: J Biol Chem Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Histona-Lisina N-Metiltransferase Limite: Humans Idioma: En Revista: J Biol Chem Ano de publicação: 2016 Tipo de documento: Article