The nuclear encoded subunits gamma, delta and epsilon from the shrimp mitochondrial F1-ATP synthase, and their transcriptional response during hypoxia

被引:6
作者
Martinez-Cruz, Oliviert [1 ]
Arvizu-Flores, Aldo [1 ]
Sotelo-Mundo, Rogerio R. [2 ]
Muhlia-Almazan, Adriana [2 ]
机构
[1] Univ Sonora, Hermosillo 83000, Sonora, Mexico
[2] Ctr Invest Alimentac & Desarrollo CIAD AC, Hermosillo, Sonora, Mexico
基金
芬兰科学院;
关键词
Genes; F-1; ATP-synthase; Nuclear subunits; Hypoxia; Shrimp; ISCHEMIA-REPERFUSION INJURY; CYTOCHROME-C-OXIDASE; ATP-SYNTHASE; LITOPENAEUS-VANNAMEI; WHITELEG SHRIMP; ESCHERICHIA-COLI; GENE-EXPRESSION; GRASS SHRIMP; HEART; SEQUENCE;
D O I
10.1007/s10863-015-9605-0
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
The mitochondrial FOF1 ATP synthase produces ATP in a reaction coupled to an electrochemical proton gradient generated by the electron transfer chain. The enzyme also hydrolyzes ATP according to the energy requirements of the organism. Shrimp need to overcome low oxygen concentrations in water and other energetic stressors, which in turn lead to mitochondrial responses. The aim of this study was to characterize the full-length cDNA sequences of three subunits that form the central stalk of the F-1 catalytic domain of the ATP synthase of the white shrimp Litopenaeus vannamei and their deduced proteins. The effect of hypoxia on shrimp was also evaluated by measuring changes in the mRNA amounts of these subunits. The cDNA sequences of the nucleus-encoded ATP gamma, ATP delta and ATP epsilon subunits are 1382, 477 and 277 bp long, respectively. The three deduced amino acid sequences exhibited highly conserved regions when compared to homologous sequences, and specific substitutions found in shrimp subunits are discussed through an homology structural model of F-1 ATP-synthase that included the five deduced proteins, which confirm their functional structures and specific characteristics from the cognate complex of ATP synthases. Genes expression was evaluated during hypoxia-reoxygenation, and resulted in a generalized down-regulation of the F-1 subunits and no coordinated changes were detected among these five subunits. The reduced mRNA levels suggest a mitochondrial response to an oxidative stress event, similar to that observed at ischemia-reperfusion in mammals. This model analysis and responses to hypoxia-reoxygenation may help to better understand additional mitochondrial adaptive mechanisms.
引用
收藏
页码:223 / 234
页数:12
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