Institute of Aquatic Economic Animals and Guangdong Province Key Laboratory for Aquatic Economic Animals, School of Life Sciences, Sun Yat-Sen University, Guangzhou, PR China.
Institute of Aquatic Economic Animals and Guangdong Province Key Laboratory for Aquatic Economic Animals, School of Life Sciences, Sun Yat-Sen University, Guangzhou, PR China; Biology Department, School of Life Sciences, Sun Yat-Sen University, Guangzhou, PR China.
Gen Comp Endocrinol. 2021 Apr 1;304:113720. doi: 10.1016/j.ygcen.2021.113720. Epub 2021 Jan 27.
G protein-coupled estrogen receptor 1 (Gper1) mediates many rapid, non-genomic estrogenic effects in vertebrates, and plays an important reproductive role in the maintenance of oocyte meiotic arrest in teleost fishes. In the present study, two genes for Gper1, namely gper1a and gper1b, were identified in the genome of a teleost fish, the ricefield eel (Monopterus albus) through Blast and syntenic analysis. Although genes neighboring gper1b are of high synteny, ricefield eel Gper1b shares very low (around 15) percent identities with Gper1 homologues of other vertebrates. In transiently transfected HEK293T cells, both ricefield eel Gper1a and Gper1b responded to estradiol (E) and estradiol-BSA (E-BSA) challenges by activating pCRE but not pSRE luciferase reporters, which were abolished by G-15 and NF-449. The production of cAMP was also increased in HEK293T cells transfected with Gper1a or Gper1b expression construct after E-BSA challenge, which was also abolished by G-15. Surprisingly, both Gper1a and Gper1b showed ligand-independent effects on pCRE luciferase reporters at higher transfected doses (10 ng). RT-PCR analysis showed that the transcript of gper1a is broadly expressed in tissues of both female and male fish while the expression of gper1b in tissues demonstrates obvious sexual dimorphism, with transcripts detected in all tissues examined in female whereas they were barely detectable in some peripheral tissues of male including the testis. In the ovary, the expression of both gper1a and gper1b was detected in the oocyte but not the follicular layer, with the mRNA levels increased during vitellogenesis, peaked at the late vitellogenic stage, and decreased precipitously at the full-grown and germinal vesicle breakdown (GVBD) stages. Moreover, E and E-BSA induced cAMP production in the in vitro incubated follicles at mid-vitellogenic stage but not the GVBD stage, and the induction could be completely abolished by G-15, a Gper1 inhibitor. Taken together, these results suggest that both Gper1a and Gper1b may play important roles in the development and maturation of ovarian follicles in ricefield eels, possibly through inhibition of oocyte meiotic resumption.
G 蛋白偶联雌激素受体 1(Gper1)在脊椎动物中介导许多快速的非基因组雌激素效应,并在维持鱼类卵母细胞减数分裂阻滞中发挥重要的生殖作用。在本研究中,通过 Blast 和基因同线性分析,在一种鱼类——日本鳗鲡(Monopterus albus)的基因组中鉴定出两种 Gper1 基因,即 gper1a 和 gper1b。尽管 gper1b 附近的基因具有高度同线性,但日本鳗鲡 Gper1b 与其他脊椎动物的 Gper1 同源物的相似度非常低(约 15%)。在瞬时转染的 HEK293T 细胞中,日本鳗鲡 Gper1a 和 Gper1b 均对雌二醇(E)和雌二醇-BSA(E-BSA)挑战作出反应,通过激活 pCRE 但不激活 pSRE 荧光素酶报告基因作出反应,该反应被 G-15 和 NF-449 所阻断。在转染 Gper1a 或 Gper1b 表达构建体后,E-BSA 挑战也会增加 HEK293T 细胞中环磷酸腺苷(cAMP)的产生,该反应也被 G-15 所阻断。令人惊讶的是,在较高转染剂量(10ng)下,Gper1a 和 Gper1b 均显示出对 pCRE 荧光素酶报告基因的配体非依赖性效应。RT-PCR 分析显示,gper1a 的转录本在雌性和雄性鱼类的组织中广泛表达,而 gper1b 在组织中的表达表现出明显的性别二态性,在所有检查的组织中都检测到了 gper1b 的转录本,而在一些雄性的外周组织中几乎检测不到,包括睾丸。在卵巢中,在卵母细胞中检测到 gper1a 和 gper1b 的表达,但在卵泡层中未检测到,在卵黄发生过程中 mRNA 水平增加,在晚期卵黄发生阶段达到峰值,在完全成熟和生发泡破裂(GVBD)阶段急剧下降。此外,E 和 E-BSA 在中期卵黄发生阶段的体外孵育卵泡中诱导 cAMP 产生,但在 GVBD 阶段不诱导,该诱导作用可被 Gper1 抑制剂 G-15 完全阻断。综上所述,这些结果表明,Gper1a 和 Gper1b 可能在日本鳗鲡卵巢卵泡的发育和成熟中发挥重要作用,可能通过抑制卵母细胞减数分裂恢复。