Abstract

Alternative cassette exons are known to originate from two processes—exonization of intronic sequences and exon shuffling. Herein, we suggest an additional mechanism by which constitutively spliced exons become alternative cassette exons during evolution. We compiled a dataset of orthologous exons from human and mouse that are constitutively spliced in one species but alternatively spliced in the other. Examination of these exons suggests that the common ancestors were constitutively spliced. We show that relaxation of the 5′ splice site during evolution is one of the molecular mechanisms by which exons shift from constitutive to alternative splicing. This shift is associated with the fixation of exonic splicing regulatory sequences (ESRs) that are essential for exon definition and control the inclusion level only after the transition to alternative splicing. The effect of each ESR on splicing and the combinatorial effects between two ESRs are conserved from fish to human. Our results uncover an evolutionary pathway that increases transcriptome diversity by shifting exons from constitutive to alternative splicing.

Highlights

  • Splicing is a mechanism by which mature mRNA is formed through the removal of introns from the pre-mRNA and the ligation of exons

  • Alternative splicing can bridge the low number of protein coding genes (;24,500) and the total number of proteins generated in the human proteome (;90,000)

  • The correlation between the higher order of phenotypic diversity and alternative splicing was recently demonstrated and the origin of alternative splicing is of great interest

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Summary

Introduction

Splicing is a mechanism by which mature mRNA is formed through the removal of introns from the pre-mRNA and the ligation of exons. Four short sequences define an intron: the 59 and 39 splice sites (59ss and 39ss), the branch site (BS), and the polypyrimidine tract (PPT) [1]. Alternative splicing is a process by which more than one mRNA is produced from the same pre-mRNA [2,3]. Alternative splicing is believed to be a major source of the phenotypic complexity in higher eukaryotes [2,7]. The recent availability of genomes and transcriptomes provides data for the study of the evolution of alternative splicing

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