Literature DB >> 20395427

Sex determination in mammalian germ cells: extrinsic versus intrinsic factors.

Josephine Bowles1, Peter Koopman.   

Abstract

Mammalian germ cells do not determine their sexual fate based on their XX or XY chromosomal constitution. Instead, sexual fate is dependent on the gonadal environment in which they develop. In a fetal testis, germ cells commit to the spermatogenic programme of development during fetal life, although they do not enter meiosis until puberty. In a fetal ovary, germ cells commit to oogenesis by entering prophase of meiosis I. Although it was believed previously that germ cells are pre-programmed to enter meiosis unless they are actively prevented from doing so, recent results indicate that meiosis is triggered by a signaling molecule, retinoic acid (RA). Meiosis is avoided in the fetal testis because a male-specifically expressed enzyme actively degrades RA during the critical time period. Additional extrinsic factors are likely to influence sexual fate of the germ cells, and in particular, we postulate that an additional male-specific fate-determining factor or factors is involved. The full complement of intrinsic factors that underlie the competence of gonadal germ cells to respond to RA and other extrinsic factors is yet to be defined.

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Year:  2010        PMID: 20395427     DOI: 10.1530/REP-10-0075

Source DB:  PubMed          Journal:  Reproduction        ISSN: 1470-1626            Impact factor:   3.906


  36 in total

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Authors:  Teng Zhang; David Zarkower
Journal:  Stem Cell Res       Date:  2017-07-25       Impact factor: 2.020

Review 2.  Initiating meiosis: the case for retinoic acid.

Authors:  Michael D Griswold; Cathryn A Hogarth; Josephine Bowles; Peter Koopman
Journal:  Biol Reprod       Date:  2012-02-14       Impact factor: 4.285

Review 3.  The hydatidiform mole.

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Review 4.  Developmental underpinnings of spermatogonial stem cell establishment.

Authors:  Nathan C Law; Jon M Oatley
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5.  High histone variant H3.3 content in mouse prospermatogonia suggests a role in epigenetic reformatting.

Authors:  Michelle C W Tang; Steve Binos; Eng K Ong; Lee H Wong; Jeffrey R Mann
Journal:  Chromosoma       Date:  2014-07-10       Impact factor: 4.316

6.  Epigenetic transgenerational actions of endocrine disruptors.

Authors:  Michael K Skinner; Mohan Manikkam; Carlos Guerrero-Bosagna
Journal:  Reprod Toxicol       Date:  2010-11-03       Impact factor: 3.143

7.  Forkhead box O member FOXO1 regulates the majority of follicle-stimulating hormone responsive genes in ovarian granulosa cells.

Authors:  Maria K Herndon; Nathan C Law; Elyse M Donaubauer; Brandon Kyriss; Mary Hunzicker-Dunn
Journal:  Mol Cell Endocrinol       Date:  2016-06-17       Impact factor: 4.102

Review 8.  Cell-intrinsic reprogramming capability: gain or loss of pluripotency in germ cells.

Authors:  Masanori Imamura; Zachary Yu-Ching Lin; Hideyuki Okano
Journal:  Reprod Med Biol       Date:  2012-06-19

9.  Licensing of gametogenesis, dependent on RNA binding protein DAZL, as a gateway to sexual differentiation of fetal germ cells.

Authors:  Mark E Gill; Yueh-Chiang Hu; Yanfeng Lin; David C Page
Journal:  Proc Natl Acad Sci U S A       Date:  2011-04-19       Impact factor: 11.205

10.  AGO4 regulates entry into meiosis and influences silencing of sex chromosomes in the male mouse germline.

Authors:  Andrew J Modzelewski; Rebecca J Holmes; Stephanie Hilz; Andrew Grimson; Paula E Cohen
Journal:  Dev Cell       Date:  2012-08-02       Impact factor: 12.270

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