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Mutational bias provides a model for the evolution of Huntington's disease and predicts a general increase in disease prevalence.
Rubinsztein, D C; Amos, W; Leggo, J; Goodburn, S; Ramesar, R S; Old, J; Bontrop, R; McMahon, R; Barton, D E; Ferguson-Smith, M A.
  • Rubinsztein DC; East Anglian Regional Genetics Service Molecular Genetics Laboratory, Addenbrooke's NHS Trust, Cambridge, UK.
Nat Genet ; 7(4): 525-30, 1994 Aug.
Article en En | MEDLINE | ID: mdl-7951324
ABSTRACT
Huntington's disease (HD) correlates with abnormal expansion in a block of CAG repeats in the Huntington's disease gene. We have investigated HD evolution by typing CAG alleles in several human populations and in a variety of primates. We find that human alleles have expanded from a shorter ancestral state and exhibit unusual asymmetric length distributions. Computer simulations are used to show that the human state can be derived readily from a primate ancestor, without the need to invoke natural selection. The key element is a simple length-dependent mutational bias towards longer alleles. Our model can explain a number of empirical observations, and predicts an ever-increasing incidence of HD.
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Banco de datos: MEDLINE Asunto principal: Enfermedad de Huntington / Evolución Biológica / Modelos Genéticos / Mutación Tipo de estudio: Etiology_studies / Prevalence_studies / Prognostic_studies / Risk_factors_studies Límite: Animals / Humans Idioma: En Año: 1994 Tipo del documento: Article
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Banco de datos: MEDLINE Asunto principal: Enfermedad de Huntington / Evolución Biológica / Modelos Genéticos / Mutación Tipo de estudio: Etiology_studies / Prevalence_studies / Prognostic_studies / Risk_factors_studies Límite: Animals / Humans Idioma: En Año: 1994 Tipo del documento: Article