Abstract
Nail patella syndrome (NPS) has been shown to result from loss of function mutations within the transcription factor LMX1B. In a large NPS family a 17 bp intronic deletion encompassing a consensus branchpoint sequence was observed to segregate with the NPS phenotype. RNA analysis demonstrated that deletion of the branchpoint sequence resulted in skipping of the downstream exon. A mechanism to explain this phenomenon is presented.
Publication types
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Research Support, U.S. Gov't, P.H.S.
MeSH terms
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Alternative Splicing
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Amino Acid Sequence
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Base Sequence
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Cells, Cultured
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DNA / chemistry
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DNA / genetics
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DNA Mutational Analysis
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Exons / genetics*
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Family Health
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Homeodomain Proteins / genetics*
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Humans
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LIM-Homeodomain Proteins
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Molecular Sequence Data
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Nail-Patella Syndrome / genetics*
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RNA / genetics
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Reverse Transcriptase Polymerase Chain Reaction
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Sequence Deletion
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Transcription Factors
Substances
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Homeodomain Proteins
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LIM homeobox transcription factor 1 beta
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LIM-Homeodomain Proteins
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Transcription Factors
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RNA
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DNA