Transcriptional and post-translational activation of AMPKα by oxidative, heat, and cold stresses in the red flour beetle, Tribolium castaneum

IF 3.2 3区 生物学 Q3 CELL BIOLOGY Cell Stress & Chaperones Pub Date : 2019-11-01 Epub Date: 2019-08-10 DOI:10.1007/s12192-019-01030-x
Heng Jiang , Nan Zhang , Minxuan Chen , Xiangkun Meng , Caihong Ji , Huichen Ge , Fan Dong , Lijun Miao , Xuemei Yang , Xin Xu , Kun Qian , Jianjun Wang
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Abstract

The AMP-activated protein kinase (AMPK) has important roles in the regulation of energy metabolism, and AMPK activity and its regulation have been the focus of relevant investigations. However, functional characterization of AMPK is still limited in insects. In this study, the full-length cDNA coding AMPKα (TcAMPKα) was isolated from the red flour beetle, Tribolium castaneum. The TcAMPKα gene contains an ORF of 1581 bp encoding a protein of 526 amino acid residues, which shared conserved domain structure with Drosophila melanogaster and mammalian orthologs. Exposure of female adults to oxidative, heat, and cold stresses caused an increase in TcAMPKα mRNA expression levels and phosphorylation of Thr-173 in the activation loop. The RNAi-mediated knockdown of TcAMPKα resulted in the increased sensitivity of T. castaneum to oxidative, heat, and cold stresses. These results suggest that stress signals regulate TcAMPKα activity, and TcAMPKα plays an important role in enabling protective mechanisms and processes that confer resistance to environmental stress.
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红面粉甲虫(Tribolium castaneum)在氧化、热和冷胁迫下 AMPKα 的转录和翻译后激活
AMP激活蛋白激酶(AMPK)在能量代谢调控中具有重要作用,AMPK活性及其调控一直是相关研究的重点。然而,AMPK 在昆虫中的功能表征仍然有限。本研究从红粉甲虫(Tribolium castaneum)中分离出了编码AMPKα(TcAMPKα)的全长cDNA。TcAMPKα基因包含一个1581 bp的ORF,编码一个526个氨基酸残基的蛋白质,其结构域与黑腹果蝇和哺乳动物的同源物相同。雌性成虫暴露于氧化、热和冷胁迫时,TcAMPKα mRNA的表达水平和活化环中Thr-173的磷酸化水平会增加。RNAi- 介导的 TcAMPKα 敲除导致蓖麻对氧化、热和冷胁迫的敏感性增加。这些结果表明,应激信号可调控 TcAMPKα 的活性,而 TcAMPKα 在实现保护机制和赋予抗环境应激能力的过程中发挥着重要作用。
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来源期刊
Cell Stress & Chaperones
Cell Stress & Chaperones 生物-细胞生物学
CiteScore
7.60
自引率
2.60%
发文量
59
审稿时长
6-12 weeks
期刊介绍: Cell Stress and Chaperones is an integrative journal that bridges the gap between laboratory model systems and natural populations. The journal captures the eclectic spirit of the cellular stress response field in a single, concentrated source of current information. Major emphasis is placed on the effects of climate change on individual species in the natural environment and their capacity to adapt. This emphasis expands our focus on stress biology and medicine by linking climate change effects to research on cellular stress responses of animals, micro-organisms and plants.
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