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Moderate intergenerational and somatic instability of a 55-CTG repeat in transgenic mice

Nature Genetics volume 15, pages 190–192 (1997)Cite this article

Abstract

Myotonic dystrophy (DM) is associated with the expansion of a (CTG)n trinucleotide repeat in the 3′ untranslated region (UTR) of the DM protein kinase gene (DMPK)1. The (CTG)n repeat is polymorphic and varies in size between 5 and 37 repeats in unaffected individuals1 whereas in affected patients there are between 50 and 4,000 CTGs2,3. The size of the (CTG)n.repeat, which increases through generations, generally correlates with clinical severity and age of onset4. The instability of the CTG repeat appears to depend on its size as well as on the sex of the transmitting parent5–9. Moreover, mitotic instability analysis of different human DM tissues shows length mosaicism between different cell lineages3,6,10–14. The molecular mechanisms of triplet instability remain elusive. To investigate the role of genomic sequences in instability, we produced transgenic mice containing a 45-kb genomic segment with a 55-CTG repeat cloned from a mildly affected patient. In contrast to other mouse models containing CAG repeats within cDNAs, these mice showed both intergenerational and somatic repeat instability15–17

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Authors and Affiliations

  1. INSERM UR383, Hôpital Necker-Enfants Malades, Pavilion Maurice LAMY, 149-161 rue de Sèvres, 75743, PARIS, Cedex 15, France

    Geneviève Gourdon, Anne-Sophie Lia, Chantal Duros, Claudine Junien & Hlène Hofmann-Radvanyi

  2. UMR144, CNRS, Institut Curie, Paris, France

    François Radvanyi & Martine Blanche

  3. Centre deRecherches Thérapeutiques en Ophtalmologie, Faculté Necker, Université René Descartes Paris V, France

    Marc Abitbol

  4. Laboratoire de Biochimie, Hôpital Ambroise Paré, Boulogne, France

    Claudine Junien & Hlène Hofmann-Radvanyi

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  1. Geneviève Gourdon
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Correspondence to Claudine Junien.

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Gourdon, G., Radvanyi, F., Lia, AS. et al. Moderate intergenerational and somatic instability of a 55-CTG repeat in transgenic mice. Nat Genet 15, 190–192 (1997). https://doi.org/10.1038/ng0297-190

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