Literature DB >> 2955519

Evidence for reduced recombination on the nondisjoined chromosomes 21 in Down syndrome.

A C Warren, A Chakravarti, C Wong, S A Slaugenhaupt, S L Halloran, P C Watkins, C Metaxotou, S E Antonarakis.   

Abstract

Trisomy 21 usually results from nondisjunction during meiosis I. In order to determine whether nondisjunction results from failure of normal chromosome pairing or premature unpairing, recombination frequencies were estimated between DNA polymorphic markers on the long arm of chromosome 21 in families containing one individual with trisomy 21. The recombination frequencies on chromosomes 21 that had undergone nondisjunction were then compared to those on chromosomes 21 that had disjoined normally. The data indicate that recombination is reduced between DNA markers on nondisjoined chromosomes 21. These results are consistent with the hypothesis that reduced chiasma formation predisposes to nondisjunction, resulting in trisomy 21 in humans.

Entities:  

Mesh:

Substances:

Year:  1987        PMID: 2955519     DOI: 10.1126/science.2955519

Source DB:  PubMed          Journal:  Science        ISSN: 0036-8075            Impact factor:   47.728


  54 in total

1.  Rare etiology of autosomal recessive disease in a child with noncarrier parents.

Authors:  R V Lebo; L R Shapiro; E Y Fenerci; J M Hoover; J L Chuang; D T Chuang; D F Kronn
Journal:  Am J Hum Genet       Date:  2000-07-27       Impact factor: 11.025

2.  Obligate short-arm exchange in de novo Robertsonian translocation formation influences placement of crossovers in chromosome 21 nondisjunction.

Authors:  Sue Ann Berend; Scott L Page; William Atkinson; Christopher McCaskill; Neil E Lamb; Stephanie L Sherman; Lisa G Shaffer
Journal:  Am J Hum Genet       Date:  2002-12-23       Impact factor: 11.025

3.  Comparative study of microsatellite and cytogenetic markers for detecting the origin of the nondisjoined chromosome 21 in Down syndrome.

Authors:  M B Peterson; M Frantzen; S E Antonarakis; A C Warren; C Van Broeckhoven; A Chakravarti; T K Cox; C Lund; B Olsen; H Poulsen
Journal:  Am J Hum Genet       Date:  1992-09       Impact factor: 11.025

4.  Oocyte selection: a new model for the maternal-age dependence of Down syndrome.

Authors:  C J Zheng; B Byers
Journal:  Hum Genet       Date:  1992 Sep-Oct       Impact factor: 4.132

5.  DNA polymorphism analysis in families with recurrence of free trisomy 21.

Authors:  C G Pangalos; C C Talbot; J G Lewis; P A Adelsberger; M B Petersen; J L Serre; M O Rethoré; M C de Blois; P Parent; A A Schinzel
Journal:  Am J Hum Genet       Date:  1992-11       Impact factor: 11.025

6.  No evidence for a paternal interchromosomal effect from analysis of the origin of nondisjunction in Down syndrome patients with concomitant familial chromosome rearrangements.

Authors:  A A Schinzel; P A Adelsberger; F Binkert; S Basaran; S E Antonarakis
Journal:  Am J Hum Genet       Date:  1992-02       Impact factor: 11.025

7.  Molecular studies of non-disjunction in trisomy 16.

Authors:  T J Hassold; D Pettay; S B Freeman; M Grantham; N Takaesu
Journal:  J Med Genet       Date:  1991-03       Impact factor: 6.318

Review 8.  Meiotic origins of maternal age-related aneuploidy.

Authors:  Teresa Chiang; Richard M Schultz; Michael A Lampson
Journal:  Biol Reprod       Date:  2012-01-10       Impact factor: 4.285

9.  Detection of nondisjunction and recombination in meiotic and postmeiotic cells from XYSxr [XY,Tp(Y)1Ct] mice using multicolor fluorescence in situ hybridization.

Authors:  T Ashley; T Ried; D C Ward
Journal:  Proc Natl Acad Sci U S A       Date:  1994-01-18       Impact factor: 11.205

10.  Meiotic crossing-over in nondisjoined chromosomes of children with trisomy 21 and a congenital heart defect.

Authors:  C M Howard; G E Davies; M J Farrer; L M Cullen; M M Coleman; R Williamson; R K Wyse; R Palmer; A M Kessling
Journal:  Am J Hum Genet       Date:  1993-08       Impact factor: 11.025

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.