| Literature DB >> 24685137 |
Eric L Greer1, Sara E Beese-Sims2, Emily Brookes1, Ruggero Spadafora3, Yun Zhu4, Scott B Rothbart5, David Aristizábal-Corrales1, Shuzhen Chen1, Aimee I Badeaux1, Qiuye Jin1, Wei Wang4, Brian D Strahl5, Monica P Colaiácovo2, Yang Shi6.
Abstract
How epigenetic information is transmitted from generation to generation remains largely unknown. Deletion of the C. elegans histone H3 lysine 4 dimethyl (H3K4me2) demethylase spr-5 leads to inherited accumulation of the euchromatic H3K4me2 mark and progressive decline in fertility. Here, we identified multiple chromatin-modifying factors, including H3K4me1/me2 and H3K9me3 methyltransferases, an H3K9me3 demethylase, and an H3K9me reader, which either suppress or accelerate the progressive transgenerational phenotypes of spr-5 mutant worms. Our findings uncover a network of chromatin regulators that control the transgenerational flow of epigenetic information and suggest that the balance between euchromatic H3K4 and heterochromatic H3K9 methylation regulates transgenerational effects on fertility.Entities:
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Year: 2014 PMID: 24685137 PMCID: PMC4012616 DOI: 10.1016/j.celrep.2014.02.044
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423