Literature DB >> 17115059

In germ cells of mouse embryonic ovaries, the decision to enter meiosis precedes premeiotic DNA replication.

Andrew E Baltus1, Douglas B Menke, Yueh-Chiang Hu, Mary L Goodheart, Anne E Carpenter, Dirk G de Rooij, David C Page.   

Abstract

The transition from mitosis to meiosis is a defining juncture in the life cycle of sexually reproducing organisms. In yeast, the decision to enter meiosis is made before the single round of DNA replication that precedes the two meiotic divisions. We present genetic evidence of an analogous decision point in the germ line of a multicellular organism. The mouse Stra8 gene is expressed in germ cells of embryonic ovaries, where meiosis is initiated, but not in those of embryonic testes, where meiosis does not begin until after birth. Here we report that in female embryos lacking Stra8 gene function, the early, mitotic development of germ cells is normal, but these cells then fail to undergo premeiotic DNA replication, meiotic chromosome condensation, cohesion, synapsis and recombination. Combined with previous findings, these genetic data suggest that active differentiation of ovarian germ cells commences at a regulatory point upstream of premeiotic DNA replication.

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Year:  2006        PMID: 17115059     DOI: 10.1038/ng1919

Source DB:  PubMed          Journal:  Nat Genet        ISSN: 1061-4036            Impact factor:   38.330


  198 in total

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3.  Male differentiation of germ cells induced by embryonic age-specific Sertoli cells in mice.

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Review 4.  The key role of vitamin A in spermatogenesis.

Authors:  Cathryn A Hogarth; Michael D Griswold
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5.  Uncovering gene regulatory networks during mouse fetal germ cell development.

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6.  A spatial and temporal map of C. elegans gene expression.

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9.  Epigenetic status determines germ cell meiotic commitment in embryonic and postnatal mammalian gonads.

Authors:  Ning Wang; Jonathan L Tilly
Journal:  Cell Cycle       Date:  2010-01-27       Impact factor: 4.534

10.  Nodal/activin signaling promotes male germ cell fate and suppresses female programming in somatic cells.

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