Symmetrically dimethylated histone H3R2 promotes global transcription during minor zygotic genome activation in mouse pronuclei

• Published in: Scientific reports Vol. 11; no. 1; p. 10146
• Main Authors: Morita, Kohtaro, Hatanaka, Yuki, Ihashi, Shunya, Asano, Masahide, Miyamoto, Kei, Matsumoto, Kazuya
• Format: Journal Article
• Language: English
• Published: London Nature Publishing Group UK 12-05-2021; Nature Publishing Group; Nature Portfolio
• Subjects: 631/136; 631/136/2435; Demethylation; Developmental stages; DNA methylation; DNA-directed RNA polymerase; Embryogenesis; Embryonic growth stage; Epigenetics; Fertilization; Genomes; Histone H3; Histones; Humanities and Social Sciences; Methylation; multidisciplinary; Protamine sulfate; RNA polymerase; Science; Science (multidisciplinary); siRNA; Transcription; Zygotes
• ISSN: 2045-2322; 2045-2322
• DOI: 10.1038/s41598-021-89334-w

Paternal genome reprogramming, such as protamine–histone exchange and global DNA demethylation, is crucial for the development of fertilised embryos. Previously, our study showed that one of histone arginine methylation, asymmetrically dimethylated histone H3R17 (H3R17me2a), is necessary for epigenetic reprogramming in the mouse paternal genome. However, roles of histone arginine methylation in reprogramming after fertilisation are still poorly understood. Here, we report that H3R2me2s promotes global transcription at the 1-cell stage, referred to as minor zygotic genome activation (ZGA). The inhibition of H3R2me2s by expressing a histone H3.3 mutant H3.3R2A prevented embryonic development from the 2-cell to 4-cell stages and significantly reduced global RNA synthesis and RNA polymerase II (Pol II) activity. Consistent with this result, the expression levels of
MuERV-L
as minor ZGA transcripts were decreased by forced expression of H3.3R2A. Furthermore, treatment with an inhibitor and co-injection of siRNA to
PRMT5
and
PRMT7
also resulted in the attenuation of transcriptional activities with reduction of H3R2me2s in the pronuclei of zygotes. Interestingly, impairment of H3K4 methylation by expression of H3.3K4M resulted in a decrease of H3R2me2s in male pronuclei. Our findings suggest that H3R2me2s together with H3K4 methylation is involved in global transcription during minor ZGA in mice.