Abstract

Alternative 3′ and 5′ splice site (ss) events constitute a significant part of all alternative splicing events. These events were also found to be related to several aberrant splicing diseases. However, only few of the characteristics that distinguish these events from alternative cassette exons are known currently. In this study, we compared the characteristics of constitutive exons, alternative cassette exons, and alternative 3′ss and 5′ss exons. The results revealed that alternative 3′ss and 5′ss exons are an intermediate state between constitutive and alternative cassette exons, where the constitutive side resembles constitutive exons, and the alternative side resembles alternative cassette exons. The results also show that alternative 3′ss and 5′ss exons exhibit low levels of symmetry (frame-preserving), similar to constitutive exons, whereas the sequence between the two alternative splice sites shows high symmetry levels, similar to alternative cassette exons. In addition, flanking intronic conservation analysis revealed that exons whose alternative splice sites are at least nine nucleotides apart show a high conservation level, indicating intronic participation in the regulation of their splicing, whereas exons whose alternative splice sites are fewer than nine nucleotides apart show a low conservation level. Further examination of these exons, spanning seven vertebrate species, suggests an evolutionary model in which the alternative state is a derivative of an ancestral constitutive exon, where a mutation inside the exon or along the flanking intron resulted in the creation of a new splice site that competes with the original one, leading to alternative splice site selection. This model was validated experimentally on four exons, showing that they indeed originated from constitutive exons that acquired a new competing splice site during evolution.

Highlights

  • The human genome sequencing project has led to the understanding that total gene number is not indicative of a higher level of phenotypic complexity, as the number of human genes is ;25,000, only slightly higher than the nematode (;19,000 genes) and lower than rice (;40,000 genes) [1,2]

  • Alternative 39 and 59 splicing events in which part of the exon is alternatively included or excluded in the mRNA constitute a significant part of all alternative splicing events, and yet little is known regarding their regulation mechanism and the evolutionary background that led to their creation

  • We show that alternative 39 and 59 splice site exons resemble constitutive exons

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Summary

Introduction

The human genome sequencing project has led to the understanding that total gene number is not indicative of a higher level of phenotypic complexity, as the number of human genes is ;25,000, only slightly higher than the nematode (;19,000 genes) and lower than rice (;40,000 genes) [1,2]. Cis-acting regulatory elements called exonic splicing enhancers (ESEs) and exonic splicing silencers (ESSs; ESEs þ ESSs are termed ESRs) were found to be involved in the regulation of the alternative splicing process [8]. These elements have the major effect when located in proximity to the alternative splice site [9,10,11,12]

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