González-Verdejo C I, Die J V, Nadal S, Jiménez-Marín A, Moreno M T, Román B
IFAPA, Centro Alameda del Obispo, Area de Mejora y Biotecnologi a, 14080 Córdoba, Spain.
Anal Biochem. 2008 Aug 15;379(2):176-81. doi: 10.1016/j.ab.2008.05.003. Epub 2008 May 7.
Real-time PCR has become the method of choice for accurate and in-depth expression studies of candidate genes. To avoid bias, real-time PCR is referred to one or several internal control genes that should not fluctuate among treatments. A need for reference genes in the parasitic plant Orobanche ramosa has emerged, and the studies in this area have not yet been evaluated. In this study, the genes 18S rRNA, Or-act1, Or-tub1, and Or-ubq1 were compared in terms of expression stability using the BestKeeper software program. Among the four common endogenous control genes, Or-act1 and Or-ubq1 were the most stable in O. ramosa samples. In parallel, a study was carried out studying the expression of the transcription factor Or-MYB1 that seemed to be implicated during preinfection stages. The normalization strategy presented here is a prerequisite to accurate real-time PCR expression profiling that, among other things, opens up the possibility of studying messenger RNA levels of low-copy-number-like transcription factors.
实时荧光定量PCR已成为对候选基因进行准确深入表达研究的首选方法。为避免偏差,实时荧光定量PCR需参照一个或几个在不同处理间不应波动的内参基因。寄生植物列当对内参基因有需求,而该领域的研究尚未得到评估。在本研究中,使用BestKeeper软件程序比较了18S rRNA、Or-act1、Or-tub1和Or-ubq1基因在表达稳定性方面的差异。在这四个常见的内参基因中,Or-act1和Or-ubq1在列当样本中最稳定。同时,开展了一项研究,研究转录因子Or-MYB1在感染前阶段可能涉及的表达情况。本文提出的标准化策略是准确的实时荧光定量PCR表达谱分析的前提条件,这尤其为研究低拷贝数样转录因子的信使RNA水平开辟了可能性。