Rhee Jae-Sung, Seo Jung Soo, Raisuddin Sheikh, Ki Jang-Seu, Lee Kyun-Woo, Kim Il-Chan, Yoon Yong-Dal, Lee Jae-Seong
Department of Molecular and Environmental Bioscience, Graduate School, Hanyang University, Seoul 133-791, South Korea.
Comp Biochem Physiol C Toxicol Pharmacol. 2008 Apr;147(3):357-65. doi: 10.1016/j.cbpc.2008.01.007. Epub 2008 Jan 16.
Gonadotropin-releasing hormone (GnRH) plays a pivotal role in the regulation of reproduction in vertebrates through interaction with a specific receptor. The GnRH-stimulated gonadotropin synthesis and release are regulated by the GnRH receptors (GnRHRs). In this study, we have identified a GnRH receptor (GnRHR) gene from the hermaphroditic fish Kryptolebias marmoratus. K. marmoratus GnRHR showed typical vertebrate GnRHR domains and motifs, and its cDNA contained 1634 bp including an open reading frame (ORF) of 1263 bp encoding a putative protein of 420 amino acids. To analyze expression patterns of GnRHR gene in various tissues and developmental stages of K. marmoratus, we carried out quantitative real-time reverse transcriptase polymerase chain reaction (RT-PCR). The K. marmoratus GnRHR gene expression was detected in all the tissues of adult fish with highest level in brain and gonad. The expression of K. marmoratus GnRHR mRNA increased from stage 1 (2 day post fertilization, dpf) to stage 4 (12 dpf) but steeply decreased at hatching stage (stage 5). Expression of K. marmoratus GnRHR after exposure to endocrine-disrupting chemicals such bisphenol A (BPA, 600 microg/L for 96 h) and 4-tert-octylphenol (OP, 300 microg/L for 96 h) in hermaphrodites as well as secondary males was highly up-regulated in almost all the tissues. Another EDC, 4-nonylphenol (NP, 300 microg/L for 96 h) showed no consistent response. 17beta-estrodiol (E2, 100 ng/L for 96 h), a known natural estrogen, suppressed expression of GnRHR in most of the tissues from hermaphrodites as well as secondary males. Tamoxifen (TMX, 10 microg/L), an estrogen antagonist, on the other hand, caused upregulation of GnRHR expression in the liver of hermaphrodites and the gonad and liver of secondary males. This is the first report of a GnRHR gene from K. marmoratus and modulation of its expression by EDCs. This study provides an insight into the molecular mechanism of endocrinological functions of this unique fish.
促性腺激素释放激素(GnRH)通过与特定受体相互作用,在脊椎动物生殖调节中发挥关键作用。GnRH刺激的促性腺激素合成和释放由GnRH受体(GnRHRs)调节。在本研究中,我们从雌雄同体鱼类红树鳉(Kryptolebias marmoratus)中鉴定出一个GnRH受体(GnRHR)基因。红树鳉GnRHR显示出典型的脊椎动物GnRHR结构域和基序,其cDNA包含1634 bp,其中包括一个1263 bp的开放阅读框(ORF),编码一个推定的420个氨基酸的蛋白质。为分析GnRHR基因在红树鳉不同组织和发育阶段的表达模式,我们进行了定量实时逆转录聚合酶链反应(RT-PCR)。在成年鱼的所有组织中均检测到红树鳉GnRHR基因表达,在脑和性腺中表达水平最高。红树鳉GnRHR mRNA的表达从第1阶段(受精后2天,dpf)到第4阶段(12 dpf)增加,但在孵化阶段(第5阶段)急剧下降。在雌雄同体以及次级雄性红树鳉中,暴露于内分泌干扰化学物质如双酚A(BPA,600 μg/L,96小时)和4-叔辛基苯酚(OP,300 μg/L,96小时)后,GnRHR在几乎所有组织中的表达均高度上调。另一种内分泌干扰物4-壬基苯酚(NP,300 μg/L,96小时)未表现出一致的反应。已知的天然雌激素17β-雌二醇(E2,100 ng/L,96小时)抑制了雌雄同体以及次级雄性红树鳉大多数组织中GnRHR的表达。另一方面,雌激素拮抗剂他莫昔芬(TMX,10 μg/L)导致雌雄同体红树鳉肝脏以及次级雄性红树鳉性腺和肝脏中GnRHR表达上调。这是关于红树鳉GnRHR基因及其受内分泌干扰物调节表达的首次报道。本研究为深入了解这种独特鱼类内分泌功能的分子机制提供了线索。