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首页> 外文期刊>Comparative biochemistry and physiology, Part B. Biochemistry & molecular biology >Molecular characterization and expression of AMP-activated protein kinase in response to low-salinity stress in the Pacific white shrimp Litopenaeus vannamei
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Molecular characterization and expression of AMP-activated protein kinase in response to low-salinity stress in the Pacific white shrimp Litopenaeus vannamei

机译:太平洋白虾南美白对虾低盐胁迫下AMP活化蛋白激酶的分子表征和表达

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AMP-activated protein kinase (AMPK) serves as a major regulator of cellular energy metabolism by activating ATP production pathways and blocicing ATP consumption. However, information on AMPK genes in aquatic animals is limited. In this study, three subunits of AMPK were cloned from the Pacific white shrimp Litopenaeus vannamei. The full-length cDNAs of the alpha, beta and gamma subunits were 1617, 1243 and 3467 by long, respectively, with open reading frames of 1566, 873 and 2988 by encoding for 521, 290 and 996 amino acids, respectively. Amino acid sequence alignments of the three subunits showed that the functional domains in the L. vannamei proteins retained the highest similarity with those of other animals, at 89%, 58%, and 75%, respectively. The expression levels of the three subunits were higher in the muscle and gills than in the eyestalk and hepatopancreas. The mRNA levels of AMPK-alpha and AMPK-beta were up-regulated in the hepatopancreas and muscle after acute low-salinity stress at 3 psu for 6 h compared with control salinity at 20 psu. After 8-week salinity stress at 3 psu, AMPK-alpha and AMPIC-beta mRNA levels in the hepatopancreas were significantly higher than those of the control at 30 psu. However, in the muscle only AMPK-gamma mRNA was significantly up-regulated at low salinity relative to controls. Muscle and hepatopancreas showed increases in AMPK protein after 6 h exposure to low salinity, but there were no differences seen after long term acclimation. The change patterns of protein were slightly differing from the mRNA patterns due to the distinguishing function of individual subunits of AMPK. These findings confirm that three AMPK subunits are present in L. vannamei and that all encode proteins with conserved functional domains. The three AMPK subunits are all regulated at the transcriptional and protein levels to manage excess energy expenditure during salinity stress. (C) 2016 Elsevier Inc. All rights reserved.
机译:AMP激活的蛋白激酶(AMPK)通过激活ATP产生途径和使ATP消耗增加而成为细胞能量代谢的主要调节剂。但是,有关水生动物AMPK基因的信息有限。在这项研究中,从太平洋白虾凡纳滨对虾中克隆了AMPK的三个亚基。 α,β和γ亚基的全长cDNA长分别为1617、1243和3467,开放阅读框分别为521、290和996个氨基酸,分别为1566、873和2988。这三个亚基的氨基酸序列比对表明,南美白对虾蛋白中的功能域与其他动物的相似性最高,分别为89%,58%和75%。这三个亚基在肌肉和腮中的表达水平高于眼球和肝胰腺。与20 psu的对照盐度相比,急性低盐度胁迫在3 psu持续6 h后,肝胰腺和肌肉中AMPK-α和AMPK-β的mRNA水平上调。在3 psu盐度胁迫8周后,肝胰腺中AMPK-α和AMPIC-beta mRNA的水平显着高于30 psu的对照组。然而,在肌肉中,相对于对照,在低盐度下仅AMPK-γmRNA显着上调。肌肉和肝胰腺暴露于低盐度下6小时后,AMPK蛋白增加,但长期适应后无差异。由于AMPK各个亚基的区分功能,蛋白质的变化模式与mRNA模式略有不同。这些发现证实了南美白对虾中存在三个AMPK亚基,并且都编码具有保守功能域的蛋白质。三个AMPK亚基均在转录和蛋白质水平上受到调节,以控制盐分胁迫期间的过多能量消耗。 (C)2016 Elsevier Inc.保留所有权利。

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