Selection of reference genes for quantitative RT-PCR studies on the gonad of the bivalve mollusc Pecten maximus L.
详细信息    查看全文
文摘
For relative quantification of gene expression the mRNA levels of target genes must be normalized. The most common normalization strategy is the utilization of internal reference genes. However, the stability of reference genes must be validated for the conditions of the study. The aim of the present work is to select the best reference genes in the bivalve mollusc Pecten maximus during the reproductive cycle from a set of seven candidates: actin (act), 18S ribosomal RNA (18S), cytochrome c oxidase subunit 1 (cox1), eukaryotic translation elongation factor 1 alpha (ef1a), glyceraldehyde-3-phosphate dehydrogenase (gapdh), NADH dehydrogenase (ubiquinone) 1 alpha subcomplex subunit 7 (ndufa7), and 40S ribosomal protein SA (rpsa). In order to have samples at different stages of the reproductive cycle three specimens were sampled at approximately monthly intervals during a period of 7 months. Three different statistical models (geNorm, NormFinder and BestKeeper) have been used to analyze the results obtained by reverse transcription quantitative real time PCR (RT-qPCR). The most suitable reference genes were specific to each tissue. In P. maximus ovary ndufa7, rpsa and ef1a were the most stable genes. In P. maximus testis 18S, ndufa7 and gapdh were the best ranked reference genes.

© 2004-2018 中国地质图书馆版权所有 京ICP备05064691号 京公网安备11010802017129号

地址:北京市海淀区学院路29号 邮编:100083

电话:办公室:(+86 10)66554848;文献借阅、咨询服务、科技查新:66554700