Alternative splicing in parallel.
Nat Biotechnol. 2002 Apr;20(4):346-7.
Please login to recommend the paper.
Make a Comment
These two articles rightly emphasize that RNA splicing measures are extremely important and poorly served by array methods so far. However, there are some problems with using exon junctions for array assays as they propose. (1) Many alternatively spliced RNAs involve multiple exons (e.g. Dscam has 130 exons). (2) If you measure expression levels at two different junctions in the same gene, it is hard to tell if they actually occur together on any RNA molecule in the complex mixture; i.e the assay is only local and therefore the encoded proteins are unknown. (3) The choice of probe (critical for getting specificity) is extremely limited for junction probes relative to exon probes (often 100 times more limited).
To address these three problems, we have developed a method to amplify single molecules and ask what exons are found in each molecule in a mixture. A gene with N exons means up to N2 possible splice junctions and 2N possible RNAs. Even if only subsets are used in a given cell, one has to determine which. Our method uses only N exon probes instead of N2 junction probes to measure the whole set. We are very interested in having this new technologies available broadly. Our first paper heading
this direction has been published (pdf of Mitra & Church, 1999), and a couple more are in preparation.
To make a comment you must login or register.