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

机译:PPARβ在黄色鲶鱼Pelteobagrus fulvidraco:膳食Cu和Zn的分子表征,组织表达和转录调控

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Peroxisome proliferator-activated receptor beta (PPAR beta) is a ligand-activated transcription factor that plays critical roles in the regulation of many important physiological processes. In this study, PPAR beta was cloned and characterized in yellow catfish Pelteobagrus fulvidraco. PPAR beta 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, PPAR beta 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 alpha-helices and a small beta-sheet of 4 strands. In addition, PPAR beta 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 PPAR beta by dietary Cu and Zn levels were also investigated. Dietary Cu levels showed no significant effects on PPAR beta mRNA levels in the liver and intestine; in contrast, dietary Zn levels upregulated the hepatic PPAR beta mRNA levels, but not in the intestine. The present study serves to increase our understanding into the function of the PPAR beta gene in fish.
机译:过氧化物体增殖物激活的受体β(PPARβ)是一种配体活化的转录因子,其在许多重要生理过程的调节中起着关键作用。在这项研究中,PPARβ被克隆并表征在黄色鲶鱼蛋白质富勒科。 PPARβcDNA的长度为2350bp,具有1530bp的开放阅读框(ORF),编码509个氨基酸,5'-未转换的区域(UTR)为474bp,以及346bp的3'-UTR。类似于哺乳动物,预计PPARβ蛋白组由四个域,A / B结构域,DNA结合结构域(DBD),D域和配体结合结构域(LBD)组成。 DBD含有两个锌手指,其中八个保守的半胱氨酸残基。 LBD的预测二级结构由12个高度保守的α-螺旋和4股的小β-薄片组成。此外,PPARβ在测试组织(肝脏,心脏,肌肉,肠道,脑,脾,肾,脂肪,卵巢和鳃)上被广泛表达,但在可变水平上。此外,还研究了通过膳食Cu和Zn水平进行PPARβ的转录反应。膳食Cu水平对肝脏和肠道的PPARβmRNA水平没有显着影响;相比之下,膳食Zn水平上调肝PPARβmRNA水平,但不在肠中。本研究有助于将我们的理解增加到PPARβ基因在鱼中的功能。

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