PR Domain-containing Protein 7 (PRDM7) Is a Histone 3 Lysine 4 Trimethyltransferase

被引:23
作者
Blazer, Levi L. [1 ]
Lima-Fernandes, Evelyne [1 ]
Gibson, Elisa [1 ]
Eram, Mohammad S. [1 ]
Loppnau, Peter [1 ]
Arrowsmith, Cheryl H. [1 ,2 ,3 ]
Schapira, Matthieu [1 ,4 ]
Vedadi, Masoud [1 ,4 ]
机构
[1] Univ Toronto, Struct Genom Consortium, Toronto, ON M5G 1L7, Canada
[2] Univ Toronto, Princess Margaret Canc Ctr, Toronto, ON M5G 2M9, Canada
[3] Univ Toronto, Dept Med Biophys, Toronto, ON M5G 2M9, Canada
[4] Univ Toronto, Dept Pharmacol & Toxicol, Toronto, ON M5S 1A8, Canada
基金
加拿大创新基金会; 巴西圣保罗研究基金会; 英国惠康基金;
关键词
epigenetics; histone methylation; histone modification; substrate specificity; zinc finger; SINGLE-NUCLEOTIDE POLYMORPHISMS; MEIOTIC RECOMBINATION HOTSPOTS; ZINC-FINGER PROTEIN; MEISETZ GENE; METHYLTRANSFERASE; VARIANTS; LOCI; RIZ1; SET; DNA;
D O I
10.1074/jbc.M116.721472
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页码:13509 / 13519
页数:11
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