Population genetics of fragile X: A multiple allele model with variable risk of CGG repeat expansion
- 15 July 1994
- journal article
- Published by Wiley in American Journal of Medical Genetics
- Vol. 51 (4) , 428-435
- https://doi.org/10.1002/ajmg.1320510425
Abstract
A model of the population genetics of fragile X that incorporates an arbitrarily large number of alleles based on CGG repeat number is presented. The probability of transition from a premutation to a full mutation upon maternal transmission depends on maternal allele size, as suggested by molecular data. Transitions among various sizes of premutation alleles upon both maternal and paternal transmission are also included using empirically determined transition probabilities. Multiple paths to the final full mutation allele are allowed. Algebraic results for equilibrium allele frequencies are presented for an arbitrary number of alleles, and numerical results are presented for the case of 9 alleles. The model predicts large frequencies for alleles near the normal premutation borderline and high mutation probabilities for the first few mutational steps. The model also predicts that the approach to equilibrium allele frequencies is quite slow, and that a premutation allele typically persists for many generations in a given family before the final transition to a full mutation allele. These nonequilibrium effects are sensitive to the transition probability from large normal alleles to small premutation alleles.Keywords
This publication has 13 references indexed in Scilit:
- Heritable unstable DNA sequences and hypermethylation associated with fragile X syndrome in Japanese familiesClinical Genetics, 1993
- Inheritance of the fragile X syndrome: size of the fragile X premutation is a major determinant of the transition to full mutation.Journal of Medical Genetics, 1992
- Evidence of founder chromosomes in fragile X syndromeNature Genetics, 1992
- Population genetics of the fragile-X syndrome: multiallelic model for the FMR1 locus.Proceedings of the National Academy of Sciences, 1992
- Study of individuals possibly affected with the fragile X syndrome in a large swedish family in the 18th to 20th centuriesAmerican Journal of Medical Genetics, 1992
- Direct Diagnosis by DNA Analysis of the Fragile X Syndrome of Mental RetardationNew England Journal of Medicine, 1991
- Variation of the CGG repeat at the fragile X site results in genetic instability: Resolution of the Sherman paradoxCell, 1991
- Possible Erasure of the Imprint on a Fragile X Chromosome When Transmitted by a MaleAmerican Journal of Medical Genetics, 1991
- Fragile X families in a Northern Swedish county ‐ a genealogical study demonstrating apparent paternal transmission from the 18th centuryAmerican Journal of Medical Genetics, 1988
- Further segregation analysis of the fragile X syndrome with special reference to transmitting malesHuman Genetics, 1985