Validation of Zebrafish (Danio rerio) Reference Genes for Quantitative Real-time RT-PCR Normalization

被引:0
|
作者
Andrew DODD [1 ]
Daniel LA [1 ]
Warren C. MCNABB [2 ]
Donald R. LOVE [1 ]
机构
[1] School of Biological Sciences, University of Auckland, Private Bag 92019, Auckland 1142, New Zealand
[2] Food and Health Group, AgResearch Grasslands, Private Bag 11008, Tennant Drive, Palmerston North, New Zealand
关键词
zebrafish; quantitative real-time RT-PCR; housekeeping genes; GAPDH gene; GeNorm;
D O I
暂无
中图分类号
Q953 [动物遗传学];
学科分类号
071007 ; 090501 ;
摘要
The normalization of quantitative real time RT-PCR (qRT-PCR) is important to obtain accurate gene expression data. The most common method for qRT-PCR normalization is to use reference, or house- keeping genes. However, there is emerging evidence that even reference genes can be regulated under different conditions, qRT-PCR has only recently been used in terms of zebrafish gene expression studies and there is no validated set of reference genes. This study characterizes the expression of nine possible reference genes during zebrafish embryonic development and in a zebrafish tissue panel. All nine reference genes exhibited variable expression. The β-actin, EF1α and Rp113α genes comprise a validated reference gene panel for zebrafish developmental time course studies, and the EF1α, Rp113α and 18S rRNA genes are more suitable as a reference gene panel for zebrafish tissue analysis. Importantly, the zebrafish GAPDH gene appears unsuitable as reference gene for both types of studies.
引用
收藏
页码:384 / 390
页数:7
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