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IRP2-Hif1α/Hif2α signaling: a novel mechanism of metabolic switch from aerobic glycolysis to oxidative phosphorylation

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成果类型:
期刊论文
作者:
Li Zhu;Qionglin Zhou;Lu He;Linxi Chen
通讯作者:
Lu He<&wdkj&>Linxi Chen
作者机构:
[Li Zhu; Qionglin Zhou; Linxi Chen] Institute of Pharmacy and Pharmacology, Learning Key Laboratory for Pharmacoproteomics, Hunan Province Cooperative Innovation Center for Molecular Target New Drug Study, University of South China, Hengyang 421001, China
[Lu He] Department of Pharmacy, The First Affiliated Hospital, University of South China, Hengyang 421001, China
通讯机构:
[Lu He] D
[Linxi Chen] I
Institute of Pharmacy and Pharmacology, Learning Key Laboratory for Pharmacoproteomics, Hunan Province Cooperative Innovation Center for Molecular Target New Drug Study, University of South China , Hengyang 421001, China<&wdkj&>Department of Pharmacy, The First Affiliated Hospital, University of South China , Hengyang 421001, China
语种:
英文
关键词:
signal transduction;glycolysis;oxidative phosphorylation
期刊:
生物化学与生物物理学报
ISSN:
1672-9145
年:
2020
卷:
52
期:
10
页码:
1175-1177
基金类别:
The work was supported by the grant from the National Natural Science Foundation of China (No. 81803535).
机构署名:
本校为第一且通讯机构
院系归属:
药学与生物科学学院
摘要:
Iron regulatory protein 2 (IRP2), first separated from mouse in 1993,is a cytoplasmic iron-regulated RNA-binding protein. IRP2 is a subtype of iron regulatory proteins (IRPs). IRP2 binds to ironresponsive element (IRE) RNA sequence to maintain iron homeostasis [1]. IRP2 can easily be hydrolyzed by protease because of its unique sequence of 73 amino acids. In general, IRP2 is widely expressed in many tissues, including fat, lung, brain, stomach, liver, heart, th...

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