Department of Integrative Biology, University of Guelph, Ont. N1G 2W1, Canada.
Department of Animal Biosciences, University of Guelph, Ont. N1G 2W1, Canada.
Gen Comp Endocrinol. 2021 Sep 15;311:113842. doi: 10.1016/j.ygcen.2021.113842. Epub 2021 Jul 10.
Previous studies have implicated the nuclear progesterone receptor (Pgr or nPR) as being critical to ovulation in fishes. This study investigated the expression of Pgr in zebrafish ovarian follicles throughout development as well as putative downstream targets of Pgr by searching the promoter regions of selected genes for specific DNA sequences to which Pgr binds and acts as a transcription factor. Expression of Pgr mRNA increases dramatically as follicles grow and mature. In silico analysis of selected genes linked to ovulation showed that the prostaglandin receptors ptger4a and ptger4b contained the progesterone responsive element (PRE) GRCCGGA in their promoter regions. Studies using full-grown follicles incubated in vitro revealed that ptger4b was upregulated in response to 17,20β-P. Our studies also showed that the expression of phospholipase A2 (PLA2G4A) mRNA and protein, a key enzyme in prostaglandin synthesis, was upregulated in response to 17,20β-P treatment. pla2g4a was not found to contain a PRE, indicating that it is regulated indirectly by 17,20β-P or that it may contain an as-of-yet unidentified PRE in its promoter region. Collectively, these studies provide further evidence of the importance of Pgr during the periovulatory periods through its involvement in prostaglandin production and function by controlling expression of PLA2G4A and the receptor EP4b and that these genes appear to be regulated through the actions of 17,20β-P.
先前的研究表明核孕激素受体(Pgr 或 nPR)在鱼类排卵中起着至关重要的作用。本研究通过在选定基因的启动子区域中搜索特定的 DNA 序列,这些序列与 Pgr 结合并充当转录因子,以寻找 Pgr 的下游靶基因,从而研究了斑马鱼卵巢滤泡发育过程中 Pgr 的表达以及 Pgr 的潜在下游靶基因。随着滤泡的生长和成熟,Pgr mRNA 的表达急剧增加。对与排卵相关的选定基因的计算机分析表明,前列腺素受体 ptger4a 和 ptger4b 在其启动子区域中含有孕激素反应元件(PRE)GRCCGGA。使用体外培养的成熟滤泡进行的研究表明,ptger4b 对 17,20β-P 的反应而上调。我们的研究还表明,前列腺素合成关键酶磷脂酶 A2(PLA2G4A)mRNA 和蛋白的表达在对 17,20β-P 处理时上调。未发现 pla2g4a 含有 PRE,表明它是通过 17,20β-P 的间接调节,或者它可能在其启动子区域中含有一个尚未确定的 PRE。总的来说,这些研究通过控制 PLA2G4A 和受体 EP4b 的表达,为 Pgr 在围排卵期的重要性提供了进一步的证据,表明 Pgr 通过参与前列腺素的产生和功能,这些基因似乎通过 17,20β-P 的作用进行调节。