Abstract
We have recently shown that a third of reliably-inferred alternative mRNA isoforms are candidates for nonsense-mediated mRNA decay (NMD), an mRNA surveillance system (Lewis et al., 2003; PROC: Natl Acad. Sci. USA, 100, 189-192). Rather than being translated to yield protein, these transcripts are expected to be degraded and may be subject to regulated unproductive splicing and translation (RUST). Our initial experimental studies are consistent with these predictions and suggest an unappreciated role for NMD in several human diseases.
Publication types
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Comparative Study
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Evaluation Study
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Research Support, U.S. Gov't, P.H.S.
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Validation Study
MeSH terms
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Alternative Splicing / genetics*
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Alzheimer Disease / genetics
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Codon, Nonsense / genetics*
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Gene Expression Regulation / genetics
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Genetic Predisposition to Disease / genetics*
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Genetic Testing / methods*
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Humans
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Lymphoma / genetics
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RNA Splice Sites / genetics
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RNA Stability / genetics*
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RNA, Messenger / genetics*
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Transcription Factors / genetics*
Substances
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Codon, Nonsense
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RNA Splice Sites
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RNA, Messenger
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Transcription Factors