O'Keefe S, Schouls M, Hodgetts R
Department of Genetics, University of Alberta, Edmonton, Canada.
Dev Genet. 1995;16(1):77-84. doi: 10.1002/dvg.1020160111.
The quantitation of RNA in tissue homogenates by amplifying the product of reverse transcription (RT-PCR) is sufficiently sensitive to detect molecules in the range of 10(-1)-10(-2) amole. We describe here the steps we believe necessary to validate a protocol that used a DNA competitor and visualization of the amplification products by ethidium bromide staining. The procedure was designed to quantitate one of the tissue specific transcripts of the Dopa decarboxylase gene (Ddc) in Drosophila. We demonstrate that the amount of epidermal Ddc transcript is much lower at pupariation in several mutants of the Broad-Complex, one of the primary response loci of the moulting hormone, ecdysone. The mutant effects were allele specific and the molecular basis of one of these alleles is known. This implicates a particular family of the zinc finger proteins encoded by the locus in the hormone dependent induction of Ddc expression.
通过扩增逆转录产物(RT-PCR)对组织匀浆中的RNA进行定量,其灵敏度足以检测10^(-1)-10^(-2) 阿托摩尔范围内的分子。我们在此描述了我们认为验证一个使用DNA竞争物并通过溴化乙锭染色观察扩增产物的方案所必需的步骤。该程序旨在定量果蝇中多巴脱羧酶基因(Ddc)的一种组织特异性转录本。我们证明,在蜕皮激素蜕皮甾酮的主要反应位点之一——宽复合基因的几个突变体中,化蛹时表皮Ddc转录本的量要低得多。突变效应是等位基因特异性的,并且其中一个等位基因的分子基础是已知的。这暗示了该位点编码的特定锌指蛋白家族参与了激素依赖性Ddc表达的诱导。