Literature DB >> 1959927

A test of the production line hypothesis of mammalian oogenesis.

P E Polani1, J A Crolla.   

Abstract

Germ cells in female mammals become committed to meiosis and enter its prophase sequentially in fetal life and, according to the Production Line Hypothesis, the oocytes thus generated are released after puberty as mature ova in the same sequence as that of meiotic entry in fetu. This hypothesis in its original and complete form has a subordinate proposition that concerns chiasma (Xma) frequency; it postulates that Xma number would decrease with fetal age. Consequently, univalents would increase, leading to errors of chromosome disjunction at the first meiotic division (MI), and thus to maternal age-dependent numerical chromosome anomalies. By using an in vitro/in vivo approach, we radioactively labelled the DNA of germ cells at premeiotic synthesis as they sequentially entered meiosis, while the fetal ovaries were in culture. At the end of this in vitro phase, pachytene/diplotene (P/D) stages were studied to determine their labelled fraction. The ovaries were then transplanted to spayed females and, after the in vivo phase, mature ova were harvested and the proportion of labelled first and second meiotic metaphases (MI/MII) determined. By marking the germ cells with label while in vitro during periods equivalent to early and late gestation, and by comparing the observed proportions of labelled MI/MII with those of oocytes labelled at P/D, we concluded that, in the mouse, ova do not mature at random for release, but are formed according to a production line system in which the time of release after puberty is related to the time of entry into meiosis in fetu.

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Year:  1991        PMID: 1959927     DOI: 10.1007/bf00204931

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


  21 in total

1.  Parental age and recombination frequency in the house mouse.

Authors:  M E Wallace; F J MacSwiney; R G Edwards
Journal:  Genet Res       Date:  1976-12       Impact factor: 1.588

2.  Nondisjunction of chromosome 21.

Authors:  N Takaesu; P A Jacobs; A Cockwell; R D Blackston; S Freeman; J Nuccio; D M Kurnit; I Uchida; V Freeman; T Hassold
Journal:  Am J Med Genet Suppl       Date:  1990

3.  Chiasmata, meiotic univalents, and age in relation to aneuploid imbalance in mice.

Authors:  P E Polani; G M Jagiello
Journal:  Cytogenet Cell Genet       Date:  1976

4.  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
Journal:  Chromosoma       Date:  1987       Impact factor: 4.316

5.  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

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

Authors:  S Sugawara; K Mikamo
Journal:  Cytogenet Cell Genet       Date:  1983

Review 7.  Detailed genetic linkage map of human chromosome 21: patterns of recombination according to age and sex.

Authors:  R E Tanzi; J L Haines; J F Gusella
Journal:  Prog Clin Biol Res       Date:  1990

8.  The use of translocation-derived "marker-bivalents" for studying the origin of meiotic instability in female mice.

Authors:  P de Boer; F A van der Hoeven
Journal:  Cytogenet Cell Genet       Date:  1980

9.  Maternal ageing and nondisjunction: a comparative study of two chromosomal techniques on the formation of univalents in first meiotic metaphase oocytes of the mouse.

Authors:  S Sugawara; K Mikamo
Journal:  Chromosoma       Date:  1986       Impact factor: 4.316

10.  Further examination of the production-line hypothesis in mouse foetal oocytes. I. Inversion heterozygotes.

Authors:  C Tease; G Fisher
Journal:  Chromosoma       Date:  1986       Impact factor: 4.316

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  25 in total

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2.  Presynaptic association of Rad51 protein with selected sites in meiotic chromatin.

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3.  Germline mosaicism does not explain the maternal age effect on trisomy.

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5.  Examining variation in recombination levels in the human female: a test of the production-line hypothesis.

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Journal:  Am J Hum Genet       Date:  2014-07-03       Impact factor: 11.025

6.  Paul Polani and the development of medical genetics.

Authors:  Peter S Harper
Journal:  Hum Genet       Date:  2007-01       Impact factor: 4.132

7.  The deteriorating soma and the indispensable germline: gamete senescence and offspring fitness.

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8.  Intergenerational effects on offspring telomere length: interactions among maternal age, stress exposure and offspring sex.

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9.  Determinants of exceptional human longevity: new ideas and findings.

Authors:  Leonid A Gavrilov; Natalia S Gavrilova
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Review 10.  Search for mechanisms of exceptional human longevity.

Authors:  Natalia S Gavrilova; Leonid A Gavrilov
Journal:  Rejuvenation Res       Date:  2010 Apr-Jun       Impact factor: 4.663

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