Literature DB >> 9718331

Mutations in fibroblast growth-factor receptor 3 in sporadic cases of achondroplasia occur exclusively on the paternally derived chromosome.

D J Wilkin1, J K Szabo, R Cameron, S Henderson, G A Bellus, M L Mack, I Kaitila, J Loughlin, A Munnich, B Sykes, J Bonaventure, C A Francomano.   

Abstract

More than 97% of achondroplasia cases are caused by one of two mutations (G1138A and G1138C) in the fibroblast growth factor receptor 3 (FGFR3) gene, which results in a specific amino acid substitution, G380R. Sporadic cases of achondroplasia have been associated with advanced paternal age, suggesting that these mutations occur preferentially during spermatogenesis. We have determined the parental origin of the achondroplasia mutation in 40 sporadic cases. Three distinct 1-bp polymorphisms were identified in the FGFR3 gene, within close proximity to the achondroplasia mutation site. Ninety-nine families, each with a sporadic case of achondroplasia in a child, were analyzed in this study. In this population, the achondroplasia mutation occurred on the paternal chromosome in all 40 cases in which parental origin was unambiguous. This observation is consistent with the clinical observation of advanced paternal age resulting in new cases of achondroplasia and suggests that factors influencing DNA replication or repair during spermatogenesis, but not during oogenesis, may predispose to the occurrence of the G1138 FGFR3 mutations.

Entities:  

Mesh:

Substances:

Year:  1998        PMID: 9718331      PMCID: PMC1377389          DOI: 10.1086/302000

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


  57 in total

Review 1.  Paternal factors and schizophrenia risk: de novo mutations and imprinting.

Authors:  D Malaspina
Journal:  Schizophr Bull       Date:  2001       Impact factor: 9.306

Review 2.  Fibroblast growth factor receptor 3 mutations in achondroplasia and related forms of dwarfism.

Authors:  William A Horton; Gregory P Lunstrum
Journal:  Rev Endocr Metab Disord       Date:  2002-12       Impact factor: 6.514

3.  Typical achondroplasia secondary to a unique insertional variant of FGFR3 with in vitro demonstration of its effect on FGFR3 function.

Authors:  April N Meyer; Peggy Modaff; Clark G Wang; Elizabeth Wohler; Nara L Sobreira; Daniel J Donoghue; Richard M Pauli
Journal:  Am J Med Genet A       Date:  2020-12-02       Impact factor: 2.802

4.  Substitution rate heterogeneity and the male mutation bias.

Authors:  Sofia Berlin; Mikael Brandström; Niclas Backström; Erik Axelsson; Nick G C Smith; Hans Ellegren
Journal:  J Mol Evol       Date:  2006-02-10       Impact factor: 2.395

Review 5.  Molecular basis for skeletal variation: insights from developmental genetic studies in mice.

Authors:  C Kappen; A Neubüser; R Balling; R Finnell
Journal:  Birth Defects Res B Dev Reprod Toxicol       Date:  2007-12

6.  A germ-line-selective advantage rather than an increased mutation rate can explain some unexpectedly common human disease mutations.

Authors:  Soo-Kyung Choi; Song-Ro Yoon; Peter Calabrese; Norman Arnheim
Journal:  Proc Natl Acad Sci U S A       Date:  2008-07-16       Impact factor: 11.205

Review 7.  Base excision repair, aging and health span.

Authors:  Guogang Xu; Maryanne Herzig; Vladimir Rotrekl; Christi A Walter
Journal:  Mech Ageing Dev       Date:  2008-03-13       Impact factor: 5.432

8.  Paternal origin of FGFR3 mutations in Muenke-type craniosynostosis.

Authors:  Sahan V Rannan-Eliya; Indira B Taylor; I Marieke De Heer; Ans M W Van Den Ouweland; Steven A Wall; Andrew O M Wilkie
Journal:  Hum Genet       Date:  2004-07-07       Impact factor: 4.132

9.  Paternal age and risk of schizophrenia in adult offspring.

Authors:  Alan S Brown; Catherine A Schaefer; Richard J Wyatt; Melissa D Begg; Raymond Goetz; Michaeline A Bresnahan; Jill Harkavy-Friedman; Jack M Gorman; Dolores Malaspina; Ezra S Susser
Journal:  Am J Psychiatry       Date:  2002-09       Impact factor: 18.112

10.  Prenatal diagnosis of skeletal dysplasia due to FGFR3 gene mutations: a 9-year experience : prenatal diagnosis in FGFR3 gene.

Authors:  M J Trujillo-Tiebas; M Fenollar-Cortés; I Lorda-Sánchez; J Díaz-Recasens; A Carrillo Redondo; C Ramos-Corrales; C Ayuso
Journal:  J Assist Reprod Genet       Date:  2009-09-30       Impact factor: 3.412

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.