Computational identification of tissue-specific alternative splicing elements in mouse genes from RNA-Seq

Research output: Contribution to journalArticle

12 Citations (Scopus)

Abstract

Tissue-specific alternative splicing is a key mechanism for generating tissue-specific proteomic diversity in eukaryotes. Splicing regulatory elements (SREs) in pre-mature messenger RNA play a very important role in regulating alternative splicing. In this article, we use mouse RNA-Seq data to determine a positive data set where SREs are over-represented and a reliable negative data set where the same SREs are most likely under-represented for a specific tissue and then employ a powerful discriminative approach to identify SREs. We identified 456 putative splicing enhancers or silencers, of which 221 were predicted to be tissue-specific. Most of our tissue-specific SREs are likely different from constitutive SREs, since only 18 of our exonic splicing enhancers (ESEs) are contained in constitutive RESCUE-ESEs. A relatively small portion (20) of our SREs is included in tissue-specific SREs in human identified in two recent studies. In the analysis of position distribution of SREs, we found that a dozen of SREs were biased to a specific region. We also identified two very interesting SREs that can function as an enhancer in one tissue but a silencer in another tissue from the same intronic region. These findings provide insight into the mechanism of tissue-specific alternative splicing and give a set of valuable putative SREs for further experimental investigations.

Original languageEnglish
Pages (from-to)7895-7907
Number of pages13
JournalNucleic Acids Research
Volume38
Issue number22
DOIs
StatePublished - Dec 1 2010

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Alternative Splicing
RNA
Genes
Eukaryota
Proteomics
Messenger RNA

ASJC Scopus subject areas

  • Genetics

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Computational identification of tissue-specific alternative splicing elements in mouse genes from RNA-Seq. / Wen, Ji; Chiba, Akira; Cai, Xiaodong.

In: Nucleic Acids Research, Vol. 38, No. 22, 01.12.2010, p. 7895-7907.

Research output: Contribution to journalArticle

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