Polycomb protein SCML2 mediates paternal epigenetic inheritance through sperm chromatin

Author:

Sakashita Akihiko12,Ooga Masatoshi345,Otsuka Kai4,Maezawa So156,Takeuchi Chikara2,Wakayama Sayaka7,Wakayama Teruhiko37,Namekawa Satoshi H14ORCID

Affiliation:

1. Division of Reproductive Sciences, Division of Developmental Biology, Perinatal Institute, Cincinnati Children's Hospital Medical Center , Cincinnati , OH 45229 , USA

2. Department of Molecular Biology, Keio University School of Medicine , Tokyo 160-8582,  Japan

3. Faculty of Life and Environmental Science, University of Yamanashi , Kofu 400-8510 , Japan

4. Department of Microbiology and Molecular Genetics, University of California Davis , Davis , CA 95616 , USA

5. Department of Animal Science and Biotechnology, School of Veterinary Medicine, Azabu University , Sagamihara , Kanagawa 252-5201 , Japan

6. Faculty of Science and Technology, Department of Applied Biological Science, Tokyo University of Science , Chiba 278-8510 , Japan

7. Advanced Biotechnology Center, University of Yamanashi , Kofu 400-8510 , Japan

Abstract

Abstract Sperm chromatin retains small amounts of histones, and chromatin states of sperm mirror gene expression programs of the next generation. However, it remains largely unknown how paternal epigenetic information is transmitted through sperm chromatin. Here, we present a novel mouse model of paternal epigenetic inheritance, in which deposition of Polycomb repressive complex 2 (PRC2) mediated-repressive H3K27me3 is attenuated in the paternal germline. By applying modified methods of assisted reproductive technology using testicular sperm, we rescued infertility of mice missing Polycomb protein SCML2, which regulates germline gene expression by establishing H3K27me3 on bivalent promoters with other active marks H3K4me2/3. We profiled epigenomic states (H3K27me3 and H3K4me3) of testicular sperm and epididymal sperm, demonstrating that the epididymal pattern of the sperm epigenome is already established in testicular sperm and that SCML2 is required for this process. In F1 males of X-linked Scml2-knockout mice, which have a wild-type genotype, gene expression is dysregulated in the male germline during spermiogenesis. These dysregulated genes are targets of SCML2-mediated H3K27me3 in F0 sperm. Further, dysregulation of gene expression was observed in the mutant-derived wild-type F1 preimplantation embryos. Together, we present functional evidence that the classic epigenetic regulator Polycomb mediates paternal epigenetic inheritance through sperm chromatin.

Funder

Early-Career Scientists

Kato Memorial Bioscience Foundation Research

JST Fusion Oriented Research

Naito Foundation and Takahashi-Sangyo Foundation

Asada Science Foundation

Watanabe Foundation

Canon Foundation

NIH

NIGMS

Publisher

Oxford University Press (OUP)

Subject

Genetics

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