首页> 美国卫生研究院文献>Proceedings of the National Academy of Sciences of the United States of America >Quantitative analysis of RNA produced by slow and fast alleles of Adh in Drosophila melanogaster.
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Quantitative analysis of RNA produced by slow and fast alleles of Adh in Drosophila melanogaster.

机译:定量分析果蝇中Adh的慢等位基因和快速等位基因产生的RNA。

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摘要

The alcohol dehydrogenase (ADH) locus (Adh) of Drosophila melanogaster in polymorphic on a world-wide basis for two allozymes, Fast and Slow. This study was undertaken to determine whether the well-established difference in ADH protein concentration between the allozymes is due to a difference in mRNA levels. RNA gel blot hybridization and an RNase protection assay were used to quantify ADH mRNA levels. Each method used an Adh null mutant as an internal standard. Several Slow and Fast allele pairs of different geographic origins were analyzed. The results provide strong evidence that the ADH protein concentration difference is not accounted for by RNA level.
机译:果蝇果蝇的乙醇脱氢酶(ADH)基因座(Adh)在全球范围内具有两种和两种快速,慢速变质酶的多态性。进行这项研究来确定同工酶之间公认的ADH蛋白浓度差异是否是由于mRNA水平的差异引起的。 RNA凝胶印迹杂交和RNase保护测定用于定量ADH mRNA水平。每种方法均使用Adh空突变体作为内标。分析了几个不同地理来源的慢速和快速等位基因对。结果提供了有力的证据,证明RNA水平不能解释ADH蛋白的浓度差异。

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