The mitochondrial housekeeping gene 16S is inappropriate as an internal standard in comparative studies of rare mitochondrial transcripts using S1-nuclease protection assays

S. Ebert, Line Breumlund, R. Nau, U. Michel
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Abstract

The analysis of rare mitochondrial transcripts derived from the L-strand of the mitochondrial genome requires a sensitive method such as the S1-nuclease protection assay. We examined whether the ribosomal mitochon­drial transcript 16S is suitable as an internal standard in a multiplex S1-nuclease protection assay for the measurement of different mitochondrial transcripts. For reliable quantification of rare mitochondrial transcripts with the RNase protection assay, a minimum of 2 μg of total RNA is necessary. Standard curves of 16S RNA produced with total RNA from human kidney, liver, brain, and a human neuroblastoma cell line (SH-SY5Y) revealed dose-response relationships that were saturated already at less than 0.5 μg of total RNA. Therefore, 16S is inappropriate as an internal standard for analyzing mitochondrial transcripts with RNase protection assays when more than 0.5 μg of total RNA have to be analyzed.
线粒体内务基因16S不适合作为使用s1 -核酸酶保护测定的罕见线粒体转录本比较研究的内标准
分析来自线粒体基因组l链的罕见线粒体转录本需要一种敏感的方法,如s1核酸酶保护试验。我们研究了核糖体线粒体转录物16S是否适合作为多重s1 -核酸酶保护试验中测量不同线粒体转录物的内部标准。为了用RNase保护试验可靠地定量稀有线粒体转录物,至少需要2 μg的总RNA。用人肾、肝、脑和人神经母细胞瘤细胞系(SH-SY5Y)的总RNA制备的16S RNA的标准曲线显示,在总RNA低于0.5 μg时已经饱和。因此,当需要分析的总RNA超过0.5 μg时,16S不适合作为RNase保护实验分析线粒体转录本的内标。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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