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
增强子
基因
细胞生物学
DNA
转录因子
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 A. Rivas,Ritu Kumar,Yahui Lan,Ingrid Torregroza,Chuan He,Simone Sidoli,Todd Evans,Olivier Elemento,Danwei Huangfu
出处
期刊:Science
[American Association for the Advancement of Science]
日期:2021-04-09
卷期号:372 (6538)
被引量:83
标识
DOI:10.1126/science.abd0875
摘要
DNA methylation is essential to mammalian development, and dysregulation can cause serious pathological conditions. Key enzymes responsible for deposition and removal of DNA methylation are known, but how they cooperate to regulate the methylation landscape remains a central question. Using a knockin DNA methylation reporter, we performed a genome-wide CRISPR-Cas9 screen in human embryonic stem cells to discover DNA methylation regulators. The top screen hit was an uncharacterized gene, QSER1, which proved to be a key guardian of bivalent promoters and poised enhancers of developmental genes, especially those residing in DNA methylation valleys (or canyons). We further demonstrate genetic and biochemical interactions of QSER1 and TET1, supporting their cooperation to safeguard transcriptional and developmental programs from DNMT3-mediated de novo methylation.
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