DNA甲基化
生物
甲基化
表观遗传学
RNA导向的DNA甲基化
遗传学
表观遗传学
基因
细胞生物学
DNA
基因表达
作者
Gary Dixon,Heng Pan,Dapeng Yang,Bess P. Rosen,Therande Jashari,Nipun Verma,Julián Pulecio,Inbal Caspi,Kihyun Lee,Stephanie Stransky,Abigail Glezer,Chang Liu,Marco Rivas,Ritu Kumar,Yahui Lan,Ingrid Torregroza,Chuan He,Simone Sidoli,Todd Evans,Olivier Elemento
出处
期刊:Science
[American Association for the Advancement of Science (AAAS)]
日期:2021-04-09
卷期号:372 (6538)
被引量:107
标识
DOI:10.1126/science.abd0875
摘要
Screen identifies demethylation regulator DNA methylation was one of the first epigenetic mechanisms discovered, but there is a limited understanding of its regulation and dysregulation in the context of development and disease. Dixon et al. performed a genome-wide CRISPR-Cas9 screen in human embryonic stem cells to identify DNA methylation regulators (see the Perspective by Gu and Goodell). A top screen hit, QSER1, proved to be essential for maintaining low methylation at DNA methylation valleys, which overlap with developmental genes and broad H3K27me3 and EZH2 peaks. Mechanistic examination revealed that QSER1 and the demethylating enzyme TET1 cooperate to safeguard developmental programs from de novo methylation by the enzyme DNMT3. Science , this issue p. eabd0875 ; see also p. 128
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