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Science ; 372(6538)2021 04 09.
Article in English | MEDLINE | ID: mdl-33833093

ABSTRACT

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.


Subject(s)
DNA Methylation , DNA/metabolism , Human Embryonic Stem Cells/metabolism , CRISPR-Cas Systems , DNA (Cytosine-5-)-Methyltransferases/metabolism , DNA Methyltransferase 3A , Enhancer Elements, Genetic , Gene Expression Regulation, Developmental , Gene Knock-In Techniques , Gene Knockout Techniques , Genome, Human , Humans , Mixed Function Oxygenases/genetics , Mixed Function Oxygenases/metabolism , Promoter Regions, Genetic , Protein Binding , Proto-Oncogene Proteins/genetics , Proto-Oncogene Proteins/metabolism , Transcription, Genetic , DNA Methyltransferase 3B
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