Literature DB >> 11023867

FIGalpha, a germ cell-specific transcription factor required for ovarian follicle formation.

S M Soyal1, A Amleh, J Dean.   

Abstract

Primordial follicles are formed perinatally in mammalian ovaries and at birth represent the lifetime complement of germ cells. With cyclic periodicity, cohorts enter into a growth phase that culminates in ovulation of mature eggs, but little is known about the regulatory cascades that govern these events. FIGalpha, a transcription factor implicated in postnatal oocyte-specific gene expression, is detected as early as embryonic day 13. Mouse lines lacking FIGalpha were established by targeted mutagenesis in embryonic stem cells. Although embryonic gonadogenesis appeared normal, primordial follicles were not formed at birth, and massive depletion of oocytes resulted in shrunken ovaries and female sterility. Fig(&agr;) (the gene for FIGalpha null males have normal fertility. The additional observation that null females do not express Zp1, Zp2 or Zp3 indicates that FIGalpha plays a key regulatory role in the expression of multiple oocyte-specific genes, including those that initiate folliculogenesis and those that encode the zona pellucida required for fertilization and early embryonic survival. The persistence of FIGalpha in adult females suggests that it may regulate additional pathways that are essential for normal ovarian development.

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Year:  2000        PMID: 11023867     DOI: 10.1242/dev.127.21.4645

Source DB:  PubMed          Journal:  Development        ISSN: 0950-1991            Impact factor:   6.868


  133 in total

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Journal:  Rev Endocr Metab Disord       Date:  2002-01       Impact factor: 6.514

2.  The mammalian oocyte orchestrates the rate of ovarian follicular development.

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Journal:  Proc Natl Acad Sci U S A       Date:  2002-02-26       Impact factor: 11.205

3.  TAp73 is downregulated in oocytes from women of advanced reproductive age.

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Journal:  Cell Cycle       Date:  2011-10-01       Impact factor: 4.534

Review 4.  Epigenetic effects of endocrine-disrupting chemicals on female reproduction: an ovarian perspective.

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Journal:  Front Neuroendocrinol       Date:  2010-07-04       Impact factor: 8.606

Review 5.  The developmental origins of the mammalian ovarian reserve.

Authors:  Kathryn J Grive; Richard N Freiman
Journal:  Development       Date:  2015-08-01       Impact factor: 6.868

Review 6.  The role of spermatogonially expressed germ cell-specific genes in mammalian meiosis.

Authors:  P Jeremy Wang; Jieyan Pan
Journal:  Chromosome Res       Date:  2007       Impact factor: 5.239

7.  Primordial follicle assembly was regulated by Notch signaling pathway in the mice.

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Journal:  Mol Biol Rep       Date:  2014-01-16       Impact factor: 2.316

8.  Notch signaling regulates ovarian follicle formation and coordinates follicular growth.

Authors:  Dallas A Vanorny; Rexxi D Prasasya; Abha J Chalpe; Signe M Kilen; Kelly E Mayo
Journal:  Mol Endocrinol       Date:  2014-02-19

9.  Suppression of Notch signaling in the neonatal mouse ovary decreases primordial follicle formation.

Authors:  Daniel J Trombly; Teresa K Woodruff; Kelly E Mayo
Journal:  Endocrinology       Date:  2008-09-25       Impact factor: 4.736

Review 10.  Cumulus and granulosa cell markers of oocyte and embryo quality.

Authors:  Asli Uyar; Saioa Torrealday; Emre Seli
Journal:  Fertil Steril       Date:  2013-03-15       Impact factor: 7.329

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