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突变体后代的不育可能是由遗传的H3K4甲基化和生殖系转录改变引起的。

Sterility in the offspring of mutants may be caused by inherited H3K4 methylation and altered germline transcription.

作者信息

Dozier Jazmin, Villhauer Mattie, Carpenter Brandon

机构信息

Molecular and Cellular Biology, Kennesaw State University, Kennesaw, Georgia, United States.

出版信息

MicroPubl Biol. 2024 Oct 5;2024. doi: 10.17912/micropub.biology.001365. eCollection 2024.

Abstract

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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d3e/11489868/488d571beca2/25789430-2024-micropub.biology.001365.jpg

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