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黄颡鱼中过氧化物酶体增殖物激活受体β:分子特征、组织表达及膳食铜和锌对其转录调控

PPARβ in yellow catfish Pelteobagrus fulvidraco: molecular characterization, tissue expression and transcriptional regulation by dietary Cu and Zn.

作者信息

You Wen-Jing, Tan Xiao-Ying, Chen Guang-Hui, Wei Chuan-Chuan, Li Dan-Dan

机构信息

Key Laboratory of Freshwater Animal Breeding, Ministry of Agriculture of P.R.C., Fishery College, Huazhong Agricultural University, Wuhan, 430070, China.

出版信息

Fish Physiol Biochem. 2018 Apr;44(2):693-702. doi: 10.1007/s10695-018-0465-5. Epub 2018 Feb 1.

Abstract

Peroxisome proliferator-activated receptor beta (PPARβ) is a ligand-activated transcription factor that plays critical roles in the regulation of many important physiological processes. In this study, PPARβ was cloned and characterized in yellow catfish Pelteobagrus fulvidraco. PPARβ cDNA was 2350 bp in length with an open reading frame (ORF) of 1530 bp, encoding 509 amino acids, a 5'-untranslated region (UTR) of 474 bp, and a 3'-UTR of 346 bp. Similar to mammals, PPARβ protein was predicted to consist of four domains, the A/B domain, DNA-binding domain (DBD), D domain, and ligand-binding domain (LBD). The DBD contained two zinc fingers with eight conserved cysteine residues. The predicted secondary structure of LBD consisted of 12 highly conserved α-helices and a small β-sheet of 4 strands. In addition, PPARβ was widely expressed across the tested tissues (liver, heart, muscle, intestine, brain, spleen, kidney, fat, ovary, and gill), but at the variable levels. Furthermore, the transcriptional responses of PPARβ by dietary Cu and Zn levels were also investigated. Dietary Cu levels showed no significant effects on PPARβ mRNA levels in the liver and intestine; in contrast, dietary Zn levels upregulated the hepatic PPARβ mRNA levels, but not in the intestine. The present study serves to increase our understanding into the function of the PPARβ gene in fish.

摘要

过氧化物酶体增殖物激活受体β(PPARβ)是一种配体激活的转录因子,在许多重要生理过程的调节中发挥关键作用。在本研究中,对黄颡鱼(Pelteobagrus fulvidraco)中的PPARβ进行了克隆和表征。PPARβ cDNA长度为2350 bp,开放阅读框(ORF)为1530 bp,编码509个氨基酸,5'非翻译区(UTR)为474 bp,3'UTR为346 bp。与哺乳动物相似,PPARβ蛋白预计由四个结构域组成,即A/B结构域、DNA结合结构域(DBD)、D结构域和配体结合结构域(LBD)。DBD包含两个带有八个保守半胱氨酸残基的锌指。LBD的预测二级结构由12个高度保守的α螺旋和一个由4条链组成的小β折叠组成。此外,PPARβ在所有测试组织(肝脏、心脏、肌肉、肠道、大脑、脾脏、肾脏、脂肪、卵巢和鳃)中广泛表达,但表达水平各不相同。此外,还研究了日粮铜和锌水平对PPARβ的转录反应。日粮铜水平对肝脏和肠道中PPARβ mRNA水平没有显著影响;相反,日粮锌水平上调了肝脏中PPARβ mRNA水平,但在肠道中没有。本研究有助于增进我们对鱼类中PPARβ基因功能的了解。

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