Abstract

BackgroundAlternative splicing is an important mechanism mediating the diversified functions of genes in multicellular organisms, and such event occurs in around 40-60% of human genes. Recently, a new splice-junction wobbling mechanism was proposed that subtle modifications exist in mRNA maturation by alternatively choosing at 5'- GTNGT and 3'- NAGNAG, which created single amino acid insertion and deletion isoforms.ResultsBy browsing the Alternative Splicing Database information, we observed that most 3' alternative splice site choices occur within six nucleotides of the dominant splice site and the incidence significantly decreases further away from the dominant acceptor site. Although a lower frequency of alternative splicing occurs within the intronic region (alternative splicing at the proximal AG) than in the exonic region (alternative splicing at the distal AG), alternative AG sites located within the intronic region show stronger potential as the acceptor. These observations revealed that the choice of 3' splice sites during 3' splicing junction wobbling could depend on the distance between the duplicated AG and the branch point site (BPS). Further mutagenesis experiments demonstrated that the distance of AG-to-AG and BPS-to-AG can greatly influence 3' splice site selection. Knocking down a known alternative splicing regulator, hSlu7, failed to affect wobble splicing choices.ConclusionOur results implied that nucleotide distance between proximal and distal AG sites has an important regulatory function. In this study, we showed that occurrence of 3' wobble splicing occurs in a distance-dependent manner and that most of this wobble splicing is probably caused by steric hindrance from a factor bound at the neighboring tandem motif sequence.

Highlights

  • Alternative splicing is an important mechanism mediating the diversified functions of genes in multicellular organisms, and such event occurs in around 40-60% of human genes

  • We found that selection of acceptor sites in 3' wobble splicing could be affected by (i) a tandem splice site (NAGNAG) and (ii) component sequences occurring between the branch point sequences (BPS) and BioMed Central tribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited

  • Occurrence of wobble splicing at tandem splice sites separated by a short distance GTNGT- and NAGNAG-based wobble splicing events are widespread in the human genome, especially the 3' wobble splicing event that, according to an expressed sequence tag (EST) database survey, occurs in 30% of human genes and is active in at least 5% of genes [7]

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Summary

Introduction

Alternative splicing is an important mechanism mediating the diversified functions of genes in multicellular organisms, and such event occurs in around 40-60% of human genes. Recent studies indicated that certain alternative 5'/3' tandem splice site selections are only a few nucleotides apart, and that such short nucleotide length variations can still lead to subtle changes in protein structure through the modification of coding amino acids [3,4,5]. This phenomenon occurs throughout the genome, which could result in many protein isoforms with one amino acid insertion or deletion [6,7,8,9,10,11,12,13,14,15]. We found that selection of acceptor sites in 3' wobble splicing could be affected by (i) a tandem splice site (NAGNAG) and (ii) component sequences occurring between the BPS and BioMed Central tribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited

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