| Literature DB >> 31748268 |
Hyo Rim Ko1,2, Inwoo Hwang1,2, Eun-Ju Jin1,2, Taegwan Yun1,2, Dongryeol Ryu1, Jong-Sun Kang1,2,3, Kye Won Park4, Joo-Ho Shin1,2,3, Sung-Woo Cho5, Kyung-Hoon Lee2,6, Keqiang Ye7, Jee-Yin Ahn8,2,3.
Abstract
ErbB3-binding protein 1 (EBP1) is implicated in diverse cellular functions, including apoptosis, cell proliferation, and differentiation. Here, by generating genetic inactivation of Ebp1 mice, we identified the physiological roles of EBP1 in vivo. Loss of Ebp1 in mice caused aberrant organogenesis, including brain malformation, and death between E13.5 and 15.5 owing to severe hemorrhages, with massive apoptosis and cessation of cell proliferation. Specific ablation of Ebp1 in neurons caused structural abnormalities of brain with neuron loss in [Nestin-Cre; Ebp1 flox/flox ] mice. Notably, global methylation increased with high levels of the gene-silencing unit Suv39H1/DNMT1 in Ebp1-deficient mice. EBP1 repressed the transcription of Dnmt1 by binding to its promoter region and interrupted DNMT1-mediated methylation at its target gene, Survivin promoter region. Reinstatement of EBP1 into embryo brain relived gene repression and rescued neuron death. Our findings uncover an essential role for EBP1 in embryonic development and implicate its function in transcriptional regulation.Entities:
Keywords: DNA methylation; Ebp1; cell death; epigenetic control; transcriptional repression
Year: 2019 PMID: 31748268 PMCID: PMC6900500 DOI: 10.1073/pnas.1916306116
Source DB: PubMed Journal: Proc Natl Acad Sci U S A ISSN: 0027-8424 Impact factor: 11.205