Abstract
Alternative pre-messenger RNA (pre-mRNA) splicing plays important roles in development, physiology, and disease, and more than half of human genes are alternatively spliced. To understand the biological roles and regulation of alternative splicing across different tissues and stages of development, systematic methods are needed. Here, we demonstrate the use of microarrays to monitor splicing at every exon-exon junction in more than 10,000 multi-exon human genes in 52 tissues and cell lines. These genome-wide data provide experimental evidence and tissue distributions for thousands of known and novel alternative splicing events. Adding to previous studies, the results indicate that at least 74% of human multi-exon genes are alternatively spliced.
MeSH terms
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Alternative Splicing*
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Amyloid beta-Protein Precursor / analysis
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Amyloid beta-Protein Precursor / genetics
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Cell Line
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DNA, Complementary
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Exons*
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Expressed Sequence Tags
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Genome, Human*
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Humans
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Hydroxymethylglutaryl CoA Reductases / analysis
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Hydroxymethylglutaryl CoA Reductases / genetics
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Molecular Sequence Data
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Oligonucleotide Array Sequence Analysis*
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Phosphoric Monoester Hydrolases*
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Protein Isoforms / analysis
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Proteins / analysis
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Proteins / genetics
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RNA Precursors / genetics*
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ROC Curve
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Reverse Transcriptase Polymerase Chain Reaction
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Tissue Distribution
Substances
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Amyloid beta-Protein Precursor
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DNA, Complementary
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Protein Isoforms
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Proteins
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RNA Precursors
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Hydroxymethylglutaryl CoA Reductases
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Phosphoric Monoester Hydrolases
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OCRL protein, human