Poyau Alain, Vincent Laurent, Berthommé Hervé, Paul Catherine, Nicolas Brigitte, Pujol Jean-François, Madjar Jean-Jacques
Institut Fédératif de Recherche 41, Ecologie, Génétique, Evolution, Développement de Techniques et Analyse Moléculaire de la Biodiversité, Université Claude Bernard-Lyon 1, Villeurbanne, France.
Electrophoresis. 2007 Aug;28(16):2843-52. doi: 10.1002/elps.200600698.
A new method has been developed allowing the identification and relative quantification of different forms of mRNA after RNA editing. This method was applied to the serotonin 2c receptor mRNA that potentially exhibits 32 different forms after adenosine to inosine editing at five different sites located in a row of 13 nucleotides. CE was used to characterize fluorescently labeled ssDNA molecules on the basis of their conformational polymorphism. The relative amount of these 32 mRNA forms has been estimated by measuring the fluorescence intensity of each individual DNA strand. Accuracy of quantification was established by diluting one form into another or into a mixture of cDNA, showing linear and precise proportion of each form (0.06 <SD <0.39%). In mouse brain tissue samples, up to 23 different mRNA forms were characterized and quantified, even for forms representing less than 1% of the mixture.
一种新方法已被开发出来,可用于识别和相对定量RNA编辑后不同形式的mRNA。该方法应用于血清素2c受体mRNA,在位于13个核苷酸序列中的五个不同位点进行腺苷到肌苷编辑后,它可能呈现32种不同形式。毛细管电泳(CE)用于根据荧光标记的单链DNA分子的构象多态性对其进行表征。通过测量每条单链DNA的荧光强度来估计这32种mRNA形式的相对含量。通过将一种形式稀释到另一种形式或cDNA混合物中来确定定量的准确性,结果显示每种形式呈线性且精确的比例(0.06 <标准差<0.39%)。在小鼠脑组织样本中,即使对于占混合物不到1%的形式,也对多达23种不同的mRNA形式进行了表征和定量。