Literature DB >> 2793171

Correlation between chromosomal breakpoint positions and synaptic behaviour in human males heterozygous for a pericentric inversion.

A de Perdigo1, O Gabriel-Robez, Y Rumpler.   

Abstract

The examination of synaptic data and localization of chromosomal breakpoints in a review of human pericentric inversions suggest that synaptic and recombination behaviour in rearranged chromosomes during meiosis can be predicted by determining the subband in which the breakpoint is located. According to this hypothesis, it can be postulated that loops in pericentric inversions are routinely formed only in cases when both breaks occur in G-light bands, with the genetic consequences of crossing-over. In other cases, heterosynapsis is accomplished without previous homosynapsis, thereby minimizing the production of unbalanced gametes.

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Year:  1989        PMID: 2793171     DOI: 10.1007/bf00285171

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


  18 in total

1.  Recurrent pole-to-pole movements of the sex chromosome during prometaphase I in Melanoplus differentialis spermatocytes.

Authors:  R B NICKLAS
Journal:  Chromosoma       Date:  1961       Impact factor: 4.316

2.  EM investigations of surface spread synaptonemal complexes in a human male carrier of a pericentric inversion inv(13)(p12q14): the role of heterosynapsis for spermatocyte survival.

Authors:  N Saadallah; M Hultén
Journal:  Ann Hum Genet       Date:  1986-10       Impact factor: 1.670

3.  Meiotic behaviour of familial pericentric inversions of chromosomes 1 and 9.

Authors:  M R Guichaoua; O Gabriel-Robez; C Ratomponirina; D Delafontaine; B Le Marec; J L Taillemite; Y Rumpler; J M Luciani
Journal:  Ann Genet       Date:  1986

Review 4.  Pericentric inversions in man. A French collaborative study. Groupe de Cytogénéticiens Français.

Authors: 
Journal:  Ann Genet       Date:  1986

5.  A model for effective pairing and recombination at meiosis based on early replicating sites (R-bands) along chromosomes.

Authors:  A C Chandley
Journal:  Hum Genet       Date:  1986-01       Impact factor: 4.132

6.  Differential elongation of autosomal pachytene bivalents related to their DNA content in human spermatocytes.

Authors:  J M Luciani; M R Guichaoua; P Cau; B Devictor; N Salagnon
Journal:  Chromosoma       Date:  1988       Impact factor: 4.316

7.  Synaptonemal complexes in a subfertile man with a pericentric inversion in chromosome 21. Heterosynapsis without previous homosynapsis.

Authors:  O Gabriel-Robez; C Ratomponirina; M Croquette; J Couturier; Y Rumpler
Journal:  Cytogenet Cell Genet       Date:  1988

8.  An extra segment in chromosome 1 of wild Mus musculus: a C-band positive homogeneously staining region.

Authors:  W Traut; H Winking; S Adolph
Journal:  Cytogenet Cell Genet       Date:  1984

9.  Electron microscopic investigations of synaptonemal complexes in an infertile human male carrier of a pericentric inversion inv(1)(p32q42). Regular loop formation but defective synapsis including a possible interchromosomal effect.

Authors:  J Batanian; M A Hulten
Journal:  Hum Genet       Date:  1987-05       Impact factor: 4.132

10.  Heterochromatin, the synaptonemal complex and crossing over.

Authors:  S M Stack
Journal:  J Cell Sci       Date:  1984-10       Impact factor: 5.285

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  11 in total

1.  Paracentric inversion of chromosome 15(q15q24): description of three families.

Authors:  E D'Alessandro; C De Matteis; M L Lo Re; M Di Cola; C Ligas; F Cappa; G Del Porto
Journal:  Hum Genet       Date:  1991-06       Impact factor: 4.132

Review 2.  Prediction of mammalian meiotic synaptic and recombinational behavior of inversion heterozygotes based on mitotic breakpoint data and the possible evolutionary consequences.

Authors:  T Ashley
Journal:  Genetica       Date:  1990       Impact factor: 1.082

Review 3.  Sperm chromosome analysis of a man heterozygous for a pericentric inversion of chromosome 20.

Authors:  J Jenderny; J Gebauer; G Röhrborn; A Rüger
Journal:  Hum Genet       Date:  1992-04       Impact factor: 4.132

4.  Molecular analysis of recombination in a family with Duchenne muscular dystrophy and a large pericentric X chromosome inversion.

Authors:  V Shashi; W L Golden; P S Allinson; S H Blanton; C von Kap-Herr; T E Kelly
Journal:  Am J Hum Genet       Date:  1996-06       Impact factor: 11.025

5.  Cri-du-Chat Syndrome Cytogenetically Cryptic Recombination Aneusomy of Chromosome 5: Implications in Recurrence Risk Estimation.

Authors:  Y Ohnuki; C Torii; R Kosaki; T Yagihashi; H Sago; K Hayashi; K Yasukawa; T Takahashi; K Kosaki
Journal:  Mol Syndromol       Date:  2010-08-13

6.  Studies of male and female meiosis in inv(4)(p1.4;q2.3) pig carriers.

Authors:  Katia Massip; Martine Yerle; Yvon Billon; Stéphane Ferchaud; Nathalie Bonnet; Anne Calgaro; Nicolas Mary; Anne-Marie Dudez; Céline Sentenac; Christophe Plard; Alain Ducos; Alain Pinton
Journal:  Chromosome Res       Date:  2010-12-02       Impact factor: 5.239

7.  Cytogenetic analysis of sperm from a man heterozygous for a pericentric inversion, inv (3) (p25q21).

Authors:  R H Martin
Journal:  Am J Hum Genet       Date:  1991-05       Impact factor: 11.025

8.  Molecular characterization of a pericentric inversion in mouse chromosome 8 implicates telomeres as promoters of meiotic recombination.

Authors:  T Ashley; N L Cacheiro; L B Russell; D C Ward
Journal:  Chromosoma       Date:  1993-01       Impact factor: 4.316

9.  Analysis of synaptonemal complexes in a heterozygous human male carrier of a reciprocal translocation involving an acrocentric chromosome: heterosynapsis without previous homosynapsis.

Authors:  A de Perdigo; O Gabriel-Robez; Y Rumpler
Journal:  Hum Genet       Date:  1991-09       Impact factor: 4.132

10.  Analysis of sperm chromosome complements from a man heterozygous for a pericentric inversion of chromosome 1.

Authors:  R H Martin; J E Chernos; R B Lowry; H A Pattinson; L Barclay; E Ko
Journal:  Hum Genet       Date:  1994-02       Impact factor: 4.132

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