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CircPTEN-MT from PTEN regulates mitochondrial energy metabolism

摘要Phosphatase and tensin homolog(PTEN)is a multifunctional gene involved in a variety of physiological and pathological processes.Circular RNAs(circRNAs)are generated from back-splicing events during mRNA processing and participate in cell biological processes through binding to RNAs or proteins.However,PTEN-related circRNAs are largely unknown.Here,we report that circPTEN-mitochondria(MT)(hsa_circ_0002934)is a circular RNA encoded by exons 3,4,and 5 of PTEN and is a critical regulator of mitochondrial energy metabolism.CircPTEN-MT is localized to mitochondria and physically associated with leucine-rich pentatricopeptide repeat-containing protein(LRPPRC),which regulates post-transcriptional gene expression in mitochondria.Knocking down circPTEN-MT reduces the interaction of LRPPRC and steroid receptor RNA activator(SRA)stem-loop interacting RNA binding protein(SLIRP)and inhibits the polyadenylation of mitochondrial mRNA,which decreases the mRNA level of the mitochondrial complex Ⅰ subunit and reduces mitochondrial membrane potential and adenosine triphosphate production.Our data demonstrate that circPTEN-MT is an important regulator of cellular energy metabolism.This study expands our understanding of the role of PTEN,which produces both linear and circular RNAs with different and independent functions.

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作者 Danhui Ruan [1] Jiancheng Xu [2] Yang Liu [1] Juan Luo [3] Xuyang Zhao [1] Yuhua Li [1] Guangxi Wang [1] Jiawen Feng [1] Hui Liang [1] Yue Yin [4] Jianyuan Luo [5] Yuxin Yin [6] 学术成果认领
作者单位 Institute of Systems Biomedicine,Department of Pathology,School of Basic Medical Sciences,Beijing Key Laboratory of Tumor Systems Biology,Peking University International Cancer Institute,Peking-Tsinghua Center of Life Sciences,Peking University Health Science Center,Beijing 100191,China [1] Institute of Systems Biomedicine,Department of Pathology,School of Basic Medical Sciences,Beijing Key Laboratory of Tumor Systems Biology,Peking University International Cancer Institute,Peking-Tsinghua Center of Life Sciences,Peking University Health Science Center,Beijing 100191,China;Soochow University Cancer Institute,Suzhou,Jiangsu 215127,China [2] Institute of Precision Medicine,Peking University Shenzhen Hospital,Shenzhen,Guangdong 518036,China [3] Department of Pharmacology,School of Basic Medical Sciences,Peking University Health Science Center,Beijing 100191,China [4] Department of Medical Genetics,Center for Medical Genetics,School of Basic Medical Sciences,Peking University Health Science Center,Beijing 100191,China [5] Institute of Systems Biomedicine,Department of Pathology,School of Basic Medical Sciences,Beijing Key Laboratory of Tumor Systems Biology,Peking University International Cancer Institute,Peking-Tsinghua Center of Life Sciences,Peking University Health Science Center,Beijing 100191,China;Institute of Precision Medicine,Peking University Shenzhen Hospital,Shenzhen,Guangdong 518036,China [6]
栏目名称 Original Research
DOI 10.1016/j.jgg.2023.12.011
发布时间 2024-07-08
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