State Key Laboratory of Biocontrol, Institute of Aquatic Economic Animals and Guangdong Province Key Laboratory for Aquatic Economic Animals, School of Life Sciences, Sun Yat-Sen University, Guangzhou 510275, China.
State Key Laboratory of Biocontrol, Institute of Aquatic Economic Animals and Guangdong Province Key Laboratory for Aquatic Economic Animals, School of Life Sciences, Sun Yat-Sen University, Guangzhou 510275, China.
J Steroid Biochem Mol Biol. 2019 May;189:10-18. doi: 10.1016/j.jsbmb.2019.01.013. Epub 2019 Jan 31.
Estrogens exert their biological functions through the estrogen receptors (ERs). In zebrafish, three nuclear estrogen receptors (nERs) named ERα, ERβ1 and ERβ2 and one membrane-bound G protein-coupled estrogen receptor (GPER) are identified. Vitellogenin (Vtg) is predominantly expressed in liver and strongly response to the stimulation of estrogen. It has been proposed that all three nERs are functionally involved in vitellogenesis and ERα may act as the major mediator in teleost. However, the role of GPER and its interaction with nERs in this process are not yet defined in teleost species. In the present study, we provide genetic evidence for the functional significance of ERα that the expression of Vtg genes (vtg1, vtg2, vtg3) and their response to estradiol stimulation were significantly decreased in esr1 mutant zebrafish. Activation of ERβ1 and ERβ2 induced Vtg expression through ERα. Moreover, the involvement of GPER in vitellogenesis and its interaction with nERs in zebrafish were firstly proposed in this work. Activation of GPER induced Vtg genes expression while inhibition of GPER significantly attenuated the estrogenic effect on Vtg. Both treatments altered the expression levels of nERs, suggesting GPER acts interactively with nERs. Collectively, the involvement of both nERs and GPER in regulation of vitellogenesis is demonstrated. ERα is the central factor, acting interactively with ERβ1, ERβ2 and GPER, and GPER regulates vitellogenesis directly and interactively with nERs.
雌激素通过雌激素受体 (ER) 发挥其生物学功能。在斑马鱼中,已鉴定出三种核雌激素受体 (nER),分别命名为 ERα、ERβ1 和 ERβ2,以及一种膜结合的 G 蛋白偶联雌激素受体 (GPER)。卵黄蛋白原 (Vtg) 主要在肝脏中表达,并强烈响应雌激素的刺激。据推测,所有三种 nER 都参与卵黄发生,并且 ERα 可能在硬骨鱼中起主要介导作用。然而,GPER 的作用及其与 nERs 在该过程中的相互作用在硬骨鱼物种中尚未确定。在本研究中,我们提供了 ERα 功能重要性的遗传证据,即 esr1 突变体斑马鱼中 Vtg 基因 (vtg1、vtg2、vtg3) 的表达及其对雌二醇刺激的反应显著降低。ERβ1 和 ERβ2 的激活通过 ERα 诱导 Vtg 表达。此外,本工作首次提出了 GPER 在卵黄发生中的作用及其与 nERs 的相互作用。GPER 的激活诱导 Vtg 基因的表达,而 GPER 的抑制则显著减弱雌激素对 Vtg 的作用。这两种处理均改变了 nERs 的表达水平,表明 GPER 与 nERs 相互作用。总之,nERs 和 GPER 均参与了卵黄发生的调节。ERα 是中心因素,与 ERβ1、ERβ2 和 GPER 相互作用,而 GPER 直接调节卵黄发生并与 nERs 相互作用。