Literature DB >> 2744454

The influence of the Robertsonian translocation Rb(X.2)2Ad on anaphase I non-disjunction in male laboratory mice.

I D Adler, R Johannisson, H Winking.   

Abstract

A Robertsonian translocation in the mouse between the X chromosome and chromosome 2 is described. The male and female carriers of the Rb(X.2)2Ad were fertile. A homozygous/hemizygous line was maintained. The influence of the X-autosomal Robertsonian translocation on anaphase I non-disjunction in male mice was studied by chromosome counts in cells at metaphase II of meiosis and by assessment of aneuploid progeny. The results conclusively show that the inclusion of Rb2Ad in the male genome induces non-disjunction at the first meoitic division. In second metaphase cells the frequency of sex-chromosomal aneuploidy was 10.8%, and secondary spermatocytes containing two or no sex chromosome were equally frequent. The Rb2Ad males sired 3.9% sex-chromosome aneuploid progeny. The difference in aneuploidy frequencies in the germ cells and among the progeny suggests that the viability of XO and XXY individuals is reduced. The pairing configurations of chromosomes 2, Rb2Ad and Y were studied during meiotic prophase by light and electron microscopy. Trivalent pairing was seen in all well spread nuclei. Complete pairing of the acrocentric autosome 2 with the corresponding segment of the Rb2Ad chromosome was only seen in 3.2% of the cells analysed in the electron microscope. The pairing between the X and Y chromosome in the Rb2Ad males corresponded to that in males with normal karyotype. Reasons for sex-chromosomal non-disjunction despite the normal pairing pattern between the sex chromosomes may be seen in the terminal chiasma location coupled with the asynchronous separation of the sex chromosomes and the autosomes.(ABSTRACT TRUNCATED AT 250 WORDS)

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Year:  1989        PMID: 2744454     DOI: 10.1017/s0016672300027944

Source DB:  PubMed          Journal:  Genet Res        ISSN: 0016-6723            Impact factor:   1.588


  5 in total

1.  Female meiosis drives karyotypic evolution in mammals.

Authors:  F Pardo-Manuel de Villena; C Sapienza
Journal:  Genetics       Date:  2001-11       Impact factor: 4.562

2.  Maternally inherited X chromosome is not inactivated in mouse blastocysts due to parental imprinting.

Authors:  Y Goto; N Takagi
Journal:  Chromosome Res       Date:  2000       Impact factor: 5.239

3.  Nondisjunction rates and abnormal embryonic development in a mouse cross between heterozygotes carrying a (7, 18) robertsonian translocation chromosome.

Authors:  R J Oakey; P G Matteson; S Litwin; S M Tilghman; R L Nussbaum
Journal:  Genetics       Date:  1995-10       Impact factor: 4.562

4.  Variable X chromosome inactivation patterns in near-tetraploid murine EC x somatic cell hybrid cells differentiated in vitro.

Authors:  N Takagi
Journal:  Genetica       Date:  1993       Impact factor: 1.082

5.  Two new X-autosome Robertsonian translocations in the mouse. II. Sex chromosome configurations in spermatocytes of hemizygous males.

Authors:  C Tease; G Fisher
Journal:  Chromosoma       Date:  1993-09       Impact factor: 4.316

  5 in total

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