The contribution of alternative splicing probability to the coding expansion of the genome

Abstract

Alternative splicing results in the inclusion or exclusion of exons in an RNA, thereby allowing a single gene to code for multiple RNA isoforms. Genes are often composed of many exons, allowing combinatorial choice to significantly expand the coding potential of the genome. How much coding potential is gained by alternative splicing and what is the main contributor: alternative-splicing-depth or exon-count? Here we develop a splice-site-centric quantification method, allowing us to characterize transcriptome-wide alternative splicing with a simple probabilistic model, enabling species-wide comparison. We use information theory to quantify the coding potential gain and show that an increase in alternative splicing probability contributes more to transcriptome expansion than exon-count. Our results suggest that dominant isoforms are co-expressed alongside many minor isoforms. We propose that this solves two problems simultaneously, that is, expression of functional isoforms and expansion of the transcriptome landscape potentially without a direct function, but available for evolution.