Dozier Jazmin, Villhauer Mattie, Carpenter Brandon
Molecular and Cellular Biology, Kennesaw State University, Kennesaw, Georgia, United States.
MicroPubl Biol. 2024 Oct 5;2024. doi: 10.17912/micropub.biology.001365. eCollection 2024.
During maternal reprogramming of histone methylation in , H3K4me is removed by the histone demethylase, SPR-5 , and H3K9me is subsequently added by the histone methyltransferase, MET-2 . Maternal loss of SPR-5 and MET-2 causes inherited phenotypes, such as sterility, in the progeny. Here, we find that knocking down either the H3K4 methyltransferase SET-2 or the H3K36 methyltransferase MES-4 partially rescues the germline in the progeny of mutants, suggesting that the inherited sterility may be caused by inherited H3K4 methylation and altered germline transcription.
在秀丽隐杆线虫中,组蛋白甲基化的母体重编程过程中,组蛋白去甲基化酶SPR-5会去除H3K4me,随后组蛋白甲基转移酶MET-2会添加H3K9me。SPR-5和MET-2的母体缺失会导致后代出现不育等遗传表型。在此,我们发现敲低H3K4甲基转移酶SET-2或H3K36甲基转移酶MES-4可部分挽救秀丽隐杆线虫突变体后代的生殖系,这表明遗传性不育可能是由遗传性H3K4甲基化和生殖系转录改变引起的。