Yan Yi-Lin, Desvignes Thomas, Bremiller Ruth, Wilson Catherine, Dillon Danielle, High Samantha, Draper Bruce, Buck Charles Loren, Postlethwait John
Institute of Neuroscience, University of Oregon, Eugene, Oregon.
Center for Bioengineering Innovation, Northern Arizona University, Flagstaff, Arizona.
Dev Dyn. 2017 Nov;246(11):925-945. doi: 10.1002/dvdy.24579. Epub 2017 Sep 25.
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.
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.
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.
生殖细胞与体细胞之间的异常信号传导可导致生殖疾病,且依赖于包括转化生长因子-β(TGFB)家族蛋白在内的可扩散信号。TGFB家族蛋白Gsdf(性腺体细胞衍生因子)控制某些鱼类的性别决定,是介导生殖细胞/体细胞信号传导的候选因子。
斑马鱼在双潜能性腺的体细胞中表达gsdf,其表达在卵巢颗粒细胞和睾丸支持细胞中持续存在。纯合gsdf基因敲除突变体延迟离开双潜能性腺状态,但随后发育为雄性或雌性。突变雌性排出少数卵母细胞后变得不育,积累未成熟卵泡。雌性突变体储存过量脂质,并下调芳香化酶、gata4、胰岛素受体、雌激素受体以及脂质代谢、卵黄蛋白原和类固醇生物合成相关基因。突变雌性比野生型含有更少的雌激素和更多的雄激素。突变雄性可育。基因组分析表明,Gsdf、Bmp15和Gdf9起源于脊椎动物基因组复制事件中的旁系同源基因。
在斑马鱼中,gsdf调节卵巢卵泡成熟以及类固醇生物合成、肥胖、糖尿病和雌性生育相关基因的表达,导致出现模仿人类多囊卵巢综合征(PCOS)的卵巢和卵巢外表型,提示相关TGFB信号分子在PCOS病因学中发挥作用。《发育动力学》246:925 - 945, 2017年。© 2017威利期刊公司。