Literature DB >> 28856758

Gonadal soma controls ovarian follicle proliferation through Gsdf in zebrafish.

Yi-Lin Yan1, Thomas Desvignes1, Ruth Bremiller1, Catherine Wilson1, Danielle Dillon2, Samantha High1, Bruce Draper3, Charles Loren Buck2,4, John Postlethwait1.   

Abstract

BACKGROUND: Aberrant signaling between germ cells and somatic cells can lead to reproductive disease and depends on diffusible signals, including transforming growth factor-beta (TGFB) -family proteins. The TGFB-family protein Gsdf (gonadal soma derived factor) controls sex determination in some fish and is a candidate for mediating germ cell/soma signaling.
RESULTS: Zebrafish expressed gsdf in somatic cells of bipotential gonads and expression continued in ovarian granulosa cells and testicular Sertoli cells. Homozygous gsdf knockout mutants delayed leaving the bipotential gonad state, but then became a male or a female. Mutant females ovulated a few oocytes, then became sterile, accumulating immature follicles. Female mutants stored excess lipid and down-regulated aromatase, gata4, insulin receptor, estrogen receptor, and genes for lipid metabolism, vitellogenin, and steroid biosynthesis. Mutant females contained less estrogen and more androgen than wild-types. Mutant males were fertile. Genomic analysis suggests that Gsdf, Bmp15, and Gdf9, originated as paralogs in vertebrate genome duplication events.
CONCLUSIONS: In zebrafish, gsdf regulates ovarian follicle maturation and expression of genes for steroid biosynthesis, obesity, diabetes, and female fertility, leading to ovarian and extra-ovarian phenotypes that mimic human polycystic ovarian syndrome (PCOS), suggesting a role for a related TGFB signaling molecule in the etiology of PCOS. Developmental Dynamics 246:925-945, 2017.
© 2017 Wiley Periodicals, Inc. © 2017 Wiley Periodicals, Inc.

Entities:  

Keywords:  BMP15; GDF9; Sertoli cells; TGFβ; gonad development; gonadal soma germ cell interaction; granulosa cells; insulin signaling; oogenesis; ovarian follicle; polycystic ovarian syndrome (PCOS)

Mesh:

Substances:

Year:  2017        PMID: 28856758      PMCID: PMC5761338          DOI: 10.1002/dvdy.24579

Source DB:  PubMed          Journal:  Dev Dyn        ISSN: 1058-8388            Impact factor:   3.780


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