Reference gene selection for qPCR in mussel, Mytilus edulis, during gametogenesis and exogenous estrogen exposure

• DOI: 10.1007/s11356-012-0772-9
• Publication Date: 2012-01-31T08:29:56Z
• Authors: Elena Cubero-Leon; Corina M. Ciocan; Christophe Minier; Jeanette M. Rotchell
• Keywords: 0301 basic medicine; Mytilus edulis; polymerase chain reaction; Endocrine disruption; estrogenic compound; 610; mitochondrial DNA; Toxicology; Real-Time Polymerase Chain Reaction; bivalve; Gametogenesis; gametogenesis; 03 medical and health sciences; C000 Biological and Biomedical Sciences; Animals; endocrine disruptor; real time; Estradiol; software; Gene Expression Profiling; Reproducibility of Results; Estrogens; Normalization; Gene Expression Regulation; C100 - Biology; gene expression; Reference genes; Water Pollutants, Chemical; toxicology; Real-time PCR; Environmental Monitoring

The aim of this study is to develop a normalization method for real-time PCR data by analyzing the most stably expressed control genes in mussel (Mytilus edulis) reproductive tissue.To facilitate this, six candidate genes, including several commonly used in the literature, were investigated in mussels at different stages of gametogenesis and following experimental exposure to a model estrogen (17b-estradiol). GeNorm and NormFinder softwares were employed to assess the stability of the reference genes.Our results demonstrate that the most stable reference genes are not the same in mussels at different stages of gametogenesis and in experimentally E2-exposed mussels. Interestingly, HEL (helicase) and ACT (actin) mRNA expression levels were most affected by the stage of gametogenesis and yet, in molluscan studies, ACT is possibly the most frequently used reference gene.We demonstrate that the experimental results are highly dependent on the reference gene chosen and that statistically significant contrasting differences between sample groups are present or absent depending on the reference gene employed.