Abstract
Expansion of trinucleotide repeats can give rise to genetic disease. We have developed a technique, repeat expansion detection (RED), that can identify potentially pathological repeat expansion without prior knowledge of chromosomal location. Human genomic DNA is used as a template for a two–step cycling process that generates oligonucleotide multimers when expanded trinucleotide sequences are present at the level found in myotonic dystrophy and fragile–X patients. We have identified at least one new locus exhibiting trinucleotide expansion. Analysis of three families transmitting a long CTG repeat shows that the allele in these families corresponds to a locus on chromosome 18. RED constitutes a powerful tool to identify other diseases caused by this mechanism, particularly diseases associated with anticipation.
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References
Webb, T.P., Bundey, S.E., Thake, A.I. & Todd, J. The Frequency of the Fragile X Chromosome Among Schoolchildren in Coventry. Am. J. med. Genet. 23, 573–580 (1986).
Gustavson, K.H., Blomquist, H. & Holmgren, G. Prevalence of Fragile–X Syndrome in Mentally Retarded Children in a Swedish County. Am. J. med. Genet. 23, 581–588 (1986).
Harper, P.S. Myotonic Dystrophy, 2nd edn (W. B. Saunders, London, 1989).
Barany, F. Genetic Disease Detection and DNA Amplification Using Cloned Thermostable Ligase. Proc. natn. Acad. Sci. U.S.A. 88, 189–193 (1991).
Schalling, M. In Gene Expression in Neural Tissues. (ed. Conn, P. M.) 231–255 (Academic Press, New York, 1992).
Brook, J.D. et al. Molecular Basis of Myotonic Dystrophy: Expansion of a Trinucleotide (CTG) Repeat at the 3′ End of a Transcript Encoding a Protein Kinase Family Member. Cell 68, 799–808 (1992).
Verkerk, A.J.M.H. et al. Identification of a Gene (FMR-1) Containing a CGG Repeat Coincident with a Breakpoint Cluster Region Exhibiting Length Variation in Fragile X Syndrome. Cell 65, 905–914 (1991).
Hinds, H. et al. Tissue Specific Expression of FMR-1 Provides Evidence for a Functional Role in Fragile X Syndrome. Nature Genet. 3, 36–43 (1993).
Fu, Y.-H. et al. An Unstable Triplet Repeat in a Gene Related to Myotonic Muscular Dystrophy. Science 255, 1256–1258 (1992).
Mahadevan, M. et al. Myotonic Dystrophy Mutation: an Unstable CTG Repeat in the 3′ Untranslated Region of the Gene. Science 255, 1253–1255 (1992).
Richards, R.I. & Sutherland, G.R. Heritable Unstable DNA Sequences. Nature Genet. 1, 7–9 (1992).
La Spada, A.R., Wilson, E.M., Lubahn, D.B., Harding, A.E. & Fischbeck, K.H. Androgen Receptor Gene Mutations in X-linked Spinal and Bulbar Muscular Atrophy. Nature 352, 77–79 (1991).
Biancalana, F., Serville, F., Pommier, J., Julien, J. & Mandel, J.L. Moderate Instability of the Trinucleotide Repeat in Spino Bulbar Muscular Atrophy. Human molec. Genet. 1, 255–258 (1992).
The Huntington's disease Collaboration group. A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosome. Cell 72, 1–20 (1993).
Aslanidis, C. et al. Cloning of the Essential Myotonic Dystrophy Region: Mapping of the Putative Defect. Nature 355, 548–551 (1992).
Buxton, J. et al. Detection of an Unstable Fragment of DNA Specific to Individuals with Myotonic Dystrophy. Nature 355, 547–548 (1992).
Harley, H.G. et al. Expansion of an Unstable DNA Region and Phenotypic Variation in Myotonic Dystrophy. Nature 355, 545–546 (1992).
Riggins, G.J. et al. Human Genes Containing Polymorphic Trinucleotide Repeats. Nature Genet. 2, 186–191 (1992).
Beckmann, J.S. & Weber, J.L. Survey of Human and Rat Microsatellites. Genomics 12, 627–631 (1992).
Sambrook, J., Fritsch, E. & Maniatis, T. Molecular Cloning: A Laboratory Manual 3rd edn (Cold Spring Harbor Press, New York, 1989).
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Schalling, M., Hudson, T., Buetow, K. et al. Direct detection of novel expanded trinucleotide repeats in the human genome. Nat Genet 4, 135–139 (1993). https://doi.org/10.1038/ng0693-135
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DOI: https://doi.org/10.1038/ng0693-135
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