项目编号 PRJCA006785
项目标题 Nuclear translocation of mitochondrial TCA cycle enzymes modulates pluripotency via histone acetylation
涉及领域 Medical
数据类型 Epigenomics
Raw sequence reads
Genome sequencing
物种名称 Mus musculus
描述信息 Pluripotent stem cells hold great promise in regenerative medicine and developmental biology studies. Mitochondrial metabolites, including tricarboxylic acid (TCA) cycle intermediates, have been reported to play critical roles in pluripotency acquisition and transition. Here we show that enzymes of the TCA cycle, including Pdha1, Pcb, Aco2, Cs, Idh3a, Ogdh, Sdha and Mdh2, are translocated to the nucleus during pluripotency acquisition and transition. The translocated TCA cycle enzymes, particularly nuclear targeted Pdha1, could promote pluripotency acquisition and transition. Mechanistically, nuclear Phda1 increases the acetyl-CoA pool in the nucleus, leading to chromatin remodeling at pluripotency genes by enhancing histone H3 acetylation. Our results reveal an important role of mitochondrial TCA cycle enzymes in the epigenetic regulation of pluripotency that constitutes a novel mitochondria-to-nucleus retrograde signaling model in pluripotency acquisition and transition.
样品范围 Monoisolate
发布日期 2022-11-13
出版信息
PubMed ID 文章标题 杂志名称 Doi 发表年份
36460681 Nuclear localization of mitochondrial TCA cycle enzymes modulates pluripotency via histone acetylation Nature Communications 10.1038/s41467-022-35199-0 2022
项目资金来源
机构 项目类型 授权项目ID 授权项目名称
Ministry of Science and Technology of the People's Republic of China (MOST) National Key Technologies R&D Program 2018YFA0107100
提交者 Li Wei (huitu09@163.com)
提交单位 Guangzhou Institutes of Biomedicine and Health, Chinese Academy of Sciences
提交日期 2021-10-04

项目包含数据信息

资源名称 描述
BioSample (53)  show -
GSA (3) -
CRA005144 Nuclear translocation of mitochondrial TCA cycle enzymes modulates pluripotency
CRA005143 Nuclear translocation of mitochondrial TCA cycle enzymes modulates pluripotency via histone acetylation
CRA007453 Nuclear translocation of mitochondrial TCA cycle enzymes modulates somatic cell reprogramming