Set7 Is a H3K37 Methyltransferase in Schizosaccharomyces pombe and Is Required for Proper Gametogenesis

Yunpeng Shen, Damiaan E.H.F. Mevius, Rocco Caliandro, Benedetta Carrozzini, Yeonjeong Roh, Jihyeon Kim, Sunghwan Kim, Sung Chul Ha, Masayo Morishita, Eric di Luccio

Research output: Contribution to journalArticlepeer-review

8 Scopus citations

Abstract

Histone methylation by histone methyltransferases (HMTases) has a key role in transcriptional regulation. Discrepancies between the known HMTases and the histone lysine methylome suggest that HMTases remain to be identified. Here we report the discovery, characterization, and crystal structure of Schizosaccharomyces pombe Set7, an HMTase methylating the uncharted histone H3 lysine 37 (H3K37) mark. Set7 forms a dimer with its substrate-binding site structurally specific to K37, not the neighboring well-studied K36 mark. We also discovered that H3K37 methylation levels dramatically increase during gametogenesis. Set7 deletion mutant cells show defects in gametogenesis and produce the abnormal number of spores with aberrant morphology. S. pombe gametogenesis shares similarities with mammalian spermatogenesis. These findings extend our understanding of epigenetic regulation during gametogenesis and support a link between Set7, the epigenetic H3K37 methyl mark, and proper gametogenesis.

Original languageEnglish
Pages (from-to)631-638.e8
JournalStructure
Volume27
Issue number4
DOIs
StatePublished - 2 Apr 2019

Keywords

  • H3K37
  • Schizosaccharomyces pombe
  • Set7
  • crystal structure
  • gametogenesis
  • histone methyltransferase
  • homo dimer

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