Literature DB >> 8533771

Expansion of the CGG repeat in fragile X in the FMR1 gene depends on the sex of the offspring.

D Z Loesch1, R Huggins, V Petrovic, H Slater.   

Abstract

Analysis of 139 mother-to-offspring transmissions of fragile X CGG triplet repeats revealed that the repeat expansion is enhanced in mother-to-son transmissions compared with mother-to-daughter transmissions. Evidence has been based on analysis of mother-offspring differences in the size of repeat (in kb), as well as on comparisons between proportions of male and female offspring with premutations, and full mutations, inherited from mothers carrying a premutation. Mean difference in the repeat size from mother-son transmissions was 1.45 kb, compared with mother-daughter transmissions of 0.76 kb. The difference is due primarily to a greater proportion of male than female offspring with full mutation from the premutation mothers and also to a higher frequency of reduction in repeat size from mothers to daughters than from mothers to sons. Our findings suggest the possibility of an interaction of the normal X homologue in a female zygote with the FMR1 sequence on the fragile X during replication to account for the lower level of expansion in mother-to-daughter transmissions relative to mother-to-son transmissions.

Entities:  

Mesh:

Substances:

Year:  1995        PMID: 8533771      PMCID: PMC1801407     

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN: 0002-9297            Impact factor:   11.025


  24 in total

1.  Data on the CGG repeat at the fragile X site in the non-retarded Japanese population and family suggest the presence of a subgroup of normal alleles predisposing to mutate.

Authors:  T Arinami; M Asano; K Kobayashi; H Yanagi; H Hamaguchi
Journal:  Hum Genet       Date:  1993-11       Impact factor: 4.132

2.  Between-generation differences in ascertainment and penetrance: relevance to genetic hypotheses in fragile X.

Authors:  D Z Loesch; L J Sheffield; D A Hay
Journal:  Hum Genet       Date:  1993-06       Impact factor: 4.132

3.  Insert size and flanking haplotype in fragile X and normal populations: possible multiple origins for the fragile X mutation.

Authors:  J N Macpherson; H Bullman; S A Youings; P A Jacobs
Journal:  Hum Mol Genet       Date:  1994-03       Impact factor: 6.150

4.  Distribution of FMR-1 and associated microsatellite alleles in a normal Chinese population.

Authors:  N Zhong; X Liu; S Gou; G E Houck; S Li; C Dobkin; W T Brown
Journal:  Am J Med Genet       Date:  1994-07-15

5.  Genotype-phenotype relationships in fragile X syndrome: a family study.

Authors:  D Z Loesch; R Huggins; D A Hay; A K Gedeon; J C Mulley; G R Sutherland
Journal:  Am J Hum Genet       Date:  1993-11       Impact factor: 11.025

6.  The full mutation in the FMR-1 gene of male fragile X patients is absent in their sperm.

Authors:  E Reyniers; L Vits; K De Boulle; B Van Roy; D Van Velzen; E de Graaff; A J Verkerk; H Z Jorens; J K Darby; B Oostra
Journal:  Nat Genet       Date:  1993-06       Impact factor: 38.330

7.  Rapid fragile X carrier screening and prenatal diagnosis using a nonradioactive PCR test.

Authors:  W T Brown; G E Houck; A Jeziorowska; F N Levinson; X Ding; C Dobkin; N Zhong; J Henderson; S S Brooks; E C Jenkins
Journal:  JAMA       Date:  1993-10-06       Impact factor: 56.272

8.  Diagnosis of fragile X syndrome by direct mutation analysis.

Authors:  M L Väisänen; M Kähkönen; J Leisti
Journal:  Hum Genet       Date:  1994-02       Impact factor: 4.132

9.  Analysis of a CGG sequence at the FMR-1 locus in fragile X families and in the general population.

Authors:  K Snow; L K Doud; R Hagerman; R G Pergolizzi; S H Erster; S N Thibodeau
Journal:  Am J Hum Genet       Date:  1993-12       Impact factor: 11.025

10.  FRAXE and mental retardation.

Authors:  J C Mulley; S Yu; D Z Loesch; D A Hay; A Donnelly; A K Gedeon; P Carbonell; I López; G Glover; I Gabarrón
Journal:  J Med Genet       Date:  1995-03       Impact factor: 6.318

View more
  11 in total

1.  Familial transmission of the FMR1 CGG repeat.

Authors:  S L Nolin; F A Lewis; L L Ye; G E Houck; A E Glicksman; P Limprasert; S Y Li; N Zhong; A E Ashley; E Feingold; S L Sherman; W T Brown
Journal:  Am J Hum Genet       Date:  1996-12       Impact factor: 11.025

Review 2.  Fragile X syndrome. Molecular and clinical insights and treatment issues.

Authors:  R J Hagerman
Journal:  West J Med       Date:  1997-02

3.  Genetic linkage of IgA deficiency to the major histocompatibility complex: evidence for allele segregation distortion, parent-of-origin penetrance differences, and the role of anti-IgA antibodies in disease predisposition.

Authors:  I Vorechovský; A D Webster; A Plebani; L Hammarström
Journal:  Am J Hum Genet       Date:  1999-04       Impact factor: 11.025

4.  FMR1 CGG expansions: prevalence and sex ratios.

Authors:  Matthew J Maenner; Mei W Baker; Karl W Broman; Jianan Tian; Janel K Barnes; Anne Atkins; Elizabeth McPherson; Jinkuk Hong; Murray H Brilliant; Marsha R Mailick
Journal:  Am J Med Genet B Neuropsychiatr Genet       Date:  2013-06-05       Impact factor: 3.568

5.  Phenotype correlation and intergenerational dynamics of the Friedreich ataxia GAA trinucleotide repeat.

Authors:  E Monrós; M D Moltó; F Martínez; J Cañizares; J Blanca; J J Vílchez; F Prieto; R de Frutos; F Palau
Journal:  Am J Hum Genet       Date:  1997-07       Impact factor: 11.025

Review 6.  The pathophysiology of fragile X (and what it teaches us about synapses).

Authors:  Asha L Bhakar; Gül Dölen; Mark F Bear
Journal:  Annu Rev Neurosci       Date:  2012-04-05       Impact factor: 12.449

7.  A genetic study of the FMR1 gene in a Sardinian multiple sclerosis population.

Authors:  L Lorefice; S Tranquilli; G Fenu; M R Murru; J Frau; M Rolesu; G C Coghe; F Marrosu; M G Marrosu; E Cocco
Journal:  Neurol Sci       Date:  2015-07-21       Impact factor: 3.307

Review 8.  Unstable mutations in the FMR1 gene and the phenotypes.

Authors:  Danuta Loesch; Randi Hagerman
Journal:  Adv Exp Med Biol       Date:  2012       Impact factor: 2.622

9.  Expansion of the fragile X CGG repeat in females with premutation or intermediate alleles.

Authors:  Sarah L Nolin; W Ted Brown; Anne Glicksman; George E Houck; Alice D Gargano; Amy Sullivan; Valérie Biancalana; Karen Bröndum-Nielsen; Helle Hjalgrim; Elke Holinski-Feder; Frank Kooy; John Longshore; James Macpherson; Jean-Louis Mandel; Gert Matthijs; Francois Rousseau; Peter Steinbach; Marja-Leena Väisänen; Harriet von Koskull; Stephanie L Sherman
Journal:  Am J Hum Genet       Date:  2003-01-14       Impact factor: 11.025

10.  Relationships between motor scores and cognitive functioning in FMR1 female premutation X carriers indicate early involvement of cerebello-cerebral pathways.

Authors:  Elsdon Storey; Minh Q Bui; Paige Stimpson; Flora Tassone; Anna Atkinson; Danuta Z Loesch
Journal:  Cerebellum Ataxias       Date:  2021-06-11
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.