Literature DB >> 6825469

Absence of correlation between univalent formation and meiotic nondisjunction in aged female Chinese hamsters.

S Sugawara, K Mikamo.   

Abstract

The effects of maternal aging on the configuration of chiasmata, formation of univalents, and segregation of first meiotic (MI) chromosomes were investigated in young (5-8 mo) and old (16-19 mo) Chinese hamsters. Primary oocytes were collected only from mature follicles approximately 10 h before ovulation, and secondary oocytes were obtained from the oviducts 5 h after spontaneous ovulation. The average number of chiasmata per oocyte was significantly smaller in aged hamsters than in the young hamsters (P less than 0.001). Terminal chiasmata were found more frequently in the former group than in the latter one (P less than 0.001). These results coincided well with findings in the mouse. Since the 11 meiotic chromosomes could be divided into four morphologically distinguishable subgroups, it was possible to determine whether the same bivalent forming univalents at MI actually underwent nondisjunction in the following meiotic division. The incidence of both MI oocytes with a univalent pair and aneuploid MII oocytes due to first meiotic nondisjunction was significantly higher in the aged group than in the young group (P less than 0.01) and P less than 0.05, respectively). However, univalents occurred almost exclusively in the smallest metacentric chromosome group (96%), whereas nondisjunction took place nearly equally in each chromosomal subgroup. These results clearly showed that there was no correlation between the univalents seen at MI and nondisjunction during the first meiotic division.

Entities:  

Mesh:

Year:  1983        PMID: 6825469     DOI: 10.1159/000131833

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


  19 in total

Review 1.  The control of mammalian female meiosis: factors that influence chromosome segregation.

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Journal:  J Assist Reprod Genet       Date:  1998-05       Impact factor: 3.412

2.  Sex Differences in the Recombination Landscape.

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3.  Chromosome segregation at meiosis I in female T(2;4)1Gö/+ mice: no evidence for a decreased crossover frequency with maternal age.

Authors:  F Beermann; I Bartels; U Franke; I Hansmann
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4.  Meiotic nondisjunction in oocytes from aged Djungarian hamsters correlates with an alteration in meiosis rate but not in univalent formation.

Authors:  E Hummler; F Theuring; I Hansmann
Journal:  Hum Genet       Date:  1987-08       Impact factor: 4.132

5.  Trisomy 21 (Down syndrome): studying nondisjunction and meiotic recombination by using cytogenetic and molecular polymorphisms that span chromosome 21.

Authors:  G D Stewart; T J Hassold; A Berg; P Watkins; R Tanzi; D M Kurnit
Journal:  Am J Hum Genet       Date:  1988-02       Impact factor: 11.025

6.  Meiosis in the foetal mouse ovary. II. Oocyte development and age-related aneuploidy. Does a production line exist?

Authors:  R M Speed; A C Chandley
Journal:  Chromosoma       Date:  1983       Impact factor: 4.316

7.  Further examination of the production-line hypothesis in mouse foetal oocytes. II. T(14; 15)6Ca heterozygotes.

Authors:  C Tease; G Fisher
Journal:  Chromosoma       Date:  1989-01       Impact factor: 4.316

8.  Variation in meiotic recombination frequencies among human males.

Authors:  Fei Sun; Kiril Trpkov; Alfred Rademaker; Evelyn Ko; Renée H Martin
Journal:  Hum Genet       Date:  2004-12-01       Impact factor: 4.132

9.  Genetic control of mammalian meiotic recombination. I. Variation in exchange frequencies among males from inbred mouse strains.

Authors:  Kara E Koehler; Jonathan P Cherry; Audrey Lynn; Patricia A Hunt; Terry J Hassold
Journal:  Genetics       Date:  2002-09       Impact factor: 4.562

10.  A test of the production line hypothesis of mammalian oogenesis.

Authors:  P E Polani; J A Crolla
Journal:  Hum Genet       Date:  1991-11       Impact factor: 4.132

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