SHORT-COMMUNICATION Validation of reference genes for real-time quantitative PCR in tambaqui (Colossoma macropomum).

A. Nascimento, Gilvan Ferreira da Silva, G. F. Gualberto, Fernanda Loureiro de Almeida
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引用次数: 3

Abstract

Tambaqui, Colossoma macropomum, is the main native freshwater fish in Brazilian aquaculture. Therefore, intensive research pressure has been applied to the species to support new technologies for tambaqui farming. Molecular biology represents a tool that can be used to investigate every field of applied biology, from fish physiology to the effects of climate change. Based on the importance of reference genes for the relative or absolute quantification of gene transcripts, we cloned and sequenced three candidate reference genes in tambaqui (18S ribossomal RNA - 18s, glyceraldehyde-3-phosphate dehydrogenase - gapdh, and actin beta - β-actin), and validated a set of primers for each gene for use in real-time quantitative PCR. The results were evaluated by RefFinder, which indicated that β-actin is the most suitable reference gene for tambaqui among those studied, followed by 18s.
坦巴蚊实时定量PCR内参基因的短通信验证。
Tambaqui, Colossoma macropomum,是巴西水产养殖的主要本地淡水鱼。因此,对该物种进行了密集的研究压力,以支持新的坦巴基养殖技术。分子生物学代表了一种工具,可以用来研究应用生物学的各个领域,从鱼类生理学到气候变化的影响。基于内参基因对基因转录本的相对或绝对定量的重要性,我们克隆并测序了tambaqui的三个候选内参基因(18S核糖体RNA - 18S,甘油醛-3-磷酸脱氢酶- gapdh和肌动蛋白β- β- β-肌动蛋白),并验证了每个基因的一组引物用于实时定量PCR。结果表明,β-肌动蛋白是最适合的内参基因,其次是18s。
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