Department of Genetics and Pathology, The Rudbeck Laboratory, Uppsala University, SE-75185, Sweden.
Nucleic Acids Res. 2010 Sep;38(16):e163. doi: 10.1093/nar/gkq581. Epub 2010 Jun 29.
Alternative splicing creates diverse mRNA isoforms from single genes and thereby enhances complexity of transcript structure and of gene function. We describe a method called spliceotyping, which translates combinatorial mRNA splicing patterns along transcripts into a library of binary strings of nucleic acid tags that encode the exon composition of individual mRNA molecules. The exon inclusion pattern of each analyzed transcript is thus represented as binary data, and the abundance of different splice variants is registered by counts of individual molecules. The technique is illustrated in a model experiment by analyzing the splicing patterns of the adenovirus early 1A gene and the beta actin reference transcript. The method permits many genes to be analyzed in parallel and it will be valuable for elucidating the complex effects of combinatorial splicing.
选择性剪接从单个基因中创建多种 mRNA 异构体,从而增强了转录本结构和基因功能的复杂性。我们描述了一种称为剪接分型的方法,该方法将组合的 mRNA 剪接模式沿转录本转化为核酸标签的二进制字符串库,这些标签编码单个 mRNA 分子的外显子组成。因此,每个分析的转录本的外显子包含模式都表示为二进制数据,并且通过单个分子的计数来记录不同剪接变体的丰度。该技术通过分析腺病毒早期 1A 基因和β肌动蛋白参考转录本的剪接模式进行了模型实验的说明。该方法允许并行分析许多基因,并且对于阐明组合剪接的复杂影响将非常有价值。