Literature DB >> 436449

Meiotic studies of translocations causing male sterility in the mouse. II. Double heterozygotes for Robertsonian translocations.

J Forejt.   

Abstract

Unusual meiotic behavior of the XY chromosome pair was observed in sterile male mice doubly heterozygous for two Robertsonian translocations, Rb(16.17)7Bnr and Rb(8.17)1Iem. Nonrandom association between the X chromosome and the translocation configuration, ascertained from the frequencies of relevant C-band contacts, was found in 9 of 10 sterile males. Besides the nonrandom association, the XY chromosomes showed signs of impaired condensation, as judged by measurement of their lengths at diakinesis/MI of the first meiotic division. In contrast, neither nonrandom contact nor decondensation of the XY chromosomes pair was found in fertile males heterozygous for a single Robertsonian translocation, Rb1Iem or Rb7Bnr. The present observations lend indirect support to the working hypothesis advanced previously, the assumption that interference with X-chromosome inactivation is a possible cause of spermatogenic breakdown in carriers of various male-sterile chromosomal transloations. Alternative explanations of the available data, which cannot be ruled out, are briefly discussed.

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Year:  1979        PMID: 436449     DOI: 10.1159/000131322

Source DB:  PubMed          Journal:  Cytogenet Cell Genet        ISSN: 0301-0171


  17 in total

1.  Chromosomal rearrangement interferes with meiotic X chromosome inactivation.

Authors:  David Homolka; Robert Ivanek; Jana Capkova; Petr Jansa; Jiri Forejt
Journal:  Genome Res       Date:  2007-08-23       Impact factor: 9.043

2.  Pattern of ribonucleic acid synthesis in vitro in primary spermatocytes from mouse testis carrying an X-autosome translocation.

Authors:  H Jaafar; O Gabriel-Robez; Y Rumpler
Journal:  Chromosoma       Date:  1989-11       Impact factor: 4.316

3.  Pachytene analysis in a 17;21 reciprocal translocation carrier: role of the acrocentric chromosomes in male sterility.

Authors:  J M Luciani; M R Guichaoua; D Delafontaine; M O North; O Gabriel-Robez; Y Rumpler
Journal:  Hum Genet       Date:  1987-11       Impact factor: 4.132

4.  Association of the extra chromosome of tertiary trisomic male mice with the sex chromosomes during first meiotic prophase, and its significance for impairment of spermatogenesis.

Authors:  P de Boer; H E Branje
Journal:  Chromosoma       Date:  1979-08       Impact factor: 4.316

5.  Familial inv(1) (p3500q21.3) associated with azoospermia.

Authors:  H Rivera; M C Alvarez-Arratia; M Moller; M Díaz; J M Cantú
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132

6.  Synaptonemal complexes of chains and rings in mice heterozygous for multiple Robertsonian translocations.

Authors:  R Johannisson; H Winking
Journal:  Chromosome Res       Date:  1994-03       Impact factor: 5.239

7.  Accumulation of rare sex chromosome rearrangements in the African pygmy mouse, Mus (Nannomys) minutoides: a whole-arm reciprocal translocation (WART) involving an X-autosome fusion.

Authors:  Frédéric Veyrunes; Johan Watson; Terence J Robinson; Janice Britton-Davidian
Journal:  Chromosome Res       Date:  2007-02-05       Impact factor: 5.239

8.  XY pair associates with the synaptonemal complex of autosomal male-sterile translocations in pachytene spermatocytes of the mouse (Mus musculus).

Authors:  J Forejt; S Gregorová; P Goetz
Journal:  Chromosoma       Date:  1981       Impact factor: 4.316

9.  Ring chromosome 21 in healthy persons: different consequences in females and in males.

Authors:  B Dallapiccola; V De Filippis; A Notarangelo; G Perla; L Zelante
Journal:  Hum Genet       Date:  1986-07       Impact factor: 4.132

10.  A high incidence of meiotic silencing of unsynapsed chromatin is not associated with substantial pachytene loss in heterozygous male mice carrying multiple simple robertsonian translocations.

Authors:  Marcia Manterola; Jesús Page; Chiara Vasco; Soledad Berríos; María Teresa Parra; Alberto Viera; Julio S Rufas; Maurizio Zuccotti; Silvia Garagna; Raúl Fernández-Donoso
Journal:  PLoS Genet       Date:  2009-08-28       Impact factor: 5.917

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