The disordered N-terminal domain of DNMT3A recognizes H2AK119ub and is required for postnatal development

• DOI: 10.1038/s41588-022-01063-6
• Publication Date: 2022-05-09T16:02:46Z
• Authors: Tianpeng Gu; Dapeng Hao; Junsung Woo; Teng-Wei Huang; Lei Guo; Xueqiu Lin; Anna G. Guzman; Ayala Tovy; Carina Rosas; Mira Jeong; Yubin Zhou; Benjamin Deneen; Yun Huang; Wei Li; Margaret A. Goodell
• Keywords: 570; Medical Sciences; Cell Phenomena; Life Sciences; 500; DNA Methylation; Medical Cell Biology; Histones; Mice; Medical Microbiology; Medical Molecular Biology; Medical Specialties; Medicine and Health Sciences; and Immunity; Animals; Protein Isoforms; DNA Modification Methylases; Biological Phenomena

DNA methyltransferase 3a (DNMT3A) plays a crucial role during mammalian development. Two isoforms of DNMT3A are differentially expressed from stem cells to somatic tissues, but their individual functions remain largely uncharacterized. Here we report that the long isoform DNMT3A1, but not the short DNMT3A2, is essential for mouse postnatal development. DNMT3A1 binds to and regulates bivalent neurodevelopmental genes in the brain. Strikingly, Dnmt3a1 knockout perinatal lethality could be partially rescued by DNMT3A1 restoration in the nervous system. We further show that the intrinsically disordered N terminus of DNMT3A1 is required for normal development and DNA methylation at DNMT3A1-enriched regions. Mechanistically, a ubiquitin-interacting motif embedded in a putative α-helix within the N terminus binds to mono-ubiquitinated histone H2AK119, probably mediating recruitment of DNMT3A1 to Polycomb-regulated regions. These data demonstrate an isoform-specific role for DNMT3A1 in mouse postnatal development and reveal the N terminus as a necessary regulatory domain for DNMT3A1 chromatin occupancy and functions in the nervous system.