Literature DB >> 1634228

Paternal selection favoring mutant alleles of the retinoblastoma susceptibility gene.

F Munier1, M A Spence, G Pescia, A Balmer, C Gailloud, F Thonney, G van Melle, H P Rutz.   

Abstract

Penetrance and segregation rates of mutant Rb-1 alleles were assessed in all 51 members of eight kindreds with hereditary retinoblastoma by concomitant ophthalmologic examination and determination of seven intragenic restriction fragment length polymorphisms (RFLPs). Penetrance was in the range reported in the literature except for one family in which it was only 42.8%. However, the odds of transmitting a mutant Rb-1 allele from one generation to the next were 25:9 in this population, much above the Mendelian 1:1 ratio (P less than 0.025). This preferential transmission was discovered through the use of molecular information. Further analysis revealed that this distortion was due to preferential inheritance among children of male carriers (18:4, P less than 0.005). No difference from a 1:1 segregation ratio could be detected among the children of female carriers (7:5). These findings were consistent with a review of relevant data in the literature.

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Year:  1992        PMID: 1634228     DOI: 10.1007/bf00219175

Source DB:  PubMed          Journal:  Hum Genet        ISSN: 0340-6717            Impact factor:   4.132


  29 in total

1.  The conservative treatment of retinoblastoma.

Authors:  H B STALLARD
Journal:  Trans Ophthalmol Soc U K       Date:  1962

2.  Short, direct repeats at the breakpoints of deletions of the retinoblastoma gene.

Authors:  S Canning; T P Dryja
Journal:  Proc Natl Acad Sci U S A       Date:  1989-07       Impact factor: 11.205

3.  Expression of recessive alleles by chromosomal mechanisms in retinoblastoma.

Authors:  W K Cavenee; T P Dryja; R A Phillips; W F Benedict; R Godbout; B L Gallie; A L Murphree; L C Strong; R L White
Journal:  Nature       Date:  1983 Oct 27-Nov 2       Impact factor: 49.962

4.  Retinoblastoma: analysis of 235 cases.

Authors:  M Gaitan-Yanguas
Journal:  Int J Radiat Oncol Biol Phys       Date:  1978 May-Jun       Impact factor: 7.038

Review 5.  Constitutional karyotype in retinoblastoma. Case report and review of literature.

Authors:  F Munier; G Pescia; M Jotterand-Bellomo; A Balmer; C Gailloud; F Thonney
Journal:  Ophthalmic Paediatr Genet       Date:  1989-06

6.  Parental origin of mutations of the retinoblastoma gene.

Authors:  T P Dryja; S Mukai; R Petersen; J M Rapaport; D Walton; D W Yandell
Journal:  Nature       Date:  1989-06-15       Impact factor: 49.962

7.  Regional assignment of genes for human esterase D and retinoblastoma to chromosome band 13q14.

Authors:  R S Sparkes; M C Sparkes; M G Wilson; J W Towner; W Benedict; A L Murphree; J J Yunis
Journal:  Science       Date:  1980-05-30       Impact factor: 47.728

8.  Retinoblastoma and subband deletion of chromosome 13.

Authors:  J J Yunis; N Ramsay
Journal:  Am J Dis Child       Date:  1978-02

9.  Mutation and cancer: statistical study of retinoblastoma.

Authors:  A G Knudson
Journal:  Proc Natl Acad Sci U S A       Date:  1971-04       Impact factor: 11.205

10.  Human retinoblastoma susceptibility gene: cloning, identification, and sequence.

Authors:  W H Lee; R Bookstein; F Hong; L J Young; J Y Shew; E Y Lee
Journal:  Science       Date:  1987-03-13       Impact factor: 47.728

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  12 in total

1.  A parent-of-origin effect in two families with retinoblastoma is associated with a distinct splice mutation in the RB1 gene.

Authors:  Martina Klutz; Dieter Brockmann; Dietmar R Lohmann
Journal:  Am J Hum Genet       Date:  2002-05-09       Impact factor: 11.025

2.  Deletion of RB exons 24 and 25 causes low-penetrance retinoblastoma.

Authors:  R Bremner; D C Du; M J Connolly-Wilson; P Bridge; K F Ahmad; H Mostachfi; D Rushlow; J M Dunn; B L Gallie
Journal:  Am J Hum Genet       Date:  1997-09       Impact factor: 11.025

3.  Meiotic segregation analysis of RB1 alleles in retinoblastoma pedigrees by use of single-sperm typing.

Authors:  A Girardet; M S McPeek; E P Leeflang; F Munier; N Arnheim; M Claustres; F Pellestor
Journal:  Am J Hum Genet       Date:  2000-01       Impact factor: 11.025

4.  FRAXA and FRAXE: evidence against segregation distortion and for an effect of intermediate alleles on learning disability.

Authors:  J W Teague; N E Morton; N R Dennis; G Curtis; N McKechnie; J N Macpherson; A Murray; M C Pound; A J Sharrock; S A Youings; P A Jacobs
Journal:  Proc Natl Acad Sci U S A       Date:  1998-01-20       Impact factor: 11.205

5.  Parental origin-dependent, male offspring-specific transmission-ratio distortion at loci on the human X chromosome.

Authors:  A K Naumova; M Leppert; D F Barker; K Morgan; C Sapienza
Journal:  Am J Hum Genet       Date:  1998-06       Impact factor: 11.025

6.  Meiotic drive at the myotonic dystrophy and the cone-rod dystrophy loci on chromosome 19q13.3.

Authors:  C F Inglehearn; C Y Gregory
Journal:  Am J Hum Genet       Date:  1997-06       Impact factor: 11.025

7.  Molecular etiology of low-penetrance retinoblastoma in two pedigrees.

Authors:  T P Dryja; J Rapaport; T L McGee; T M Nork; T L Schwartz
Journal:  Am J Hum Genet       Date:  1993-06       Impact factor: 11.025

Review 8.  Putative non-Mendelian transmission of retinoblastoma in males: a phenotypic segregation analysis of 150 pedigrees.

Authors:  F L Munier; L Arabien; P Flodman; M A Spence; G Pescia; H P Rutz; A L Murphree
Journal:  Hum Genet       Date:  1994-11       Impact factor: 4.132

9.  The genetics of retinoblastoma, revisited.

Authors:  A Naumova; C Sapienza
Journal:  Am J Hum Genet       Date:  1994-02       Impact factor: 11.025

10.  Non-Mendelian transmission in dentatorubral-pallidoluysian atrophy and Machado-Joseph disease: the mutant allele is preferentially transmitted in male meiosis.

Authors:  T Ikeuchi; S Igarashi; Y Takiyama; O Onodera; M Oyake; H Takano; R Koide; H Tanaka; S Tsuji
Journal:  Am J Hum Genet       Date:  1996-04       Impact factor: 11.025

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