Kaiser U B, Sabbagh E, Saunders B D, Chin W W
Department of Medicine, Brigham and Women's Hospital and Harvard Medical School, Boston, Massachusetts 02115, USA.
Endocrinology. 1998 May;139(5):2443-51. doi: 10.1210/endo.139.5.6003.
GnRH plays a critical role in reproductive development and function by regulating the biosynthesis and secretion of the pituitary gonadotropins, LH and FSH. Although it is known that GnRH induces gonadotropin subunit gene transcription, the mechanism by which this occurs has not been elucidated. Studies have been hindered by the lack of available cell lines that express the LH and FSH subunit genes and respond to GnRH. We have transfected the rat pituitary GH3 cell line with the rat GnRH receptor complementary DNA. These cells, when cotransfected with regulatory regions of the LH or FSH subunit genes fused to a luciferase reporter gene, respond to GnRH with an increase in promoter activity comparable to that seen in primary rat pituitary cells. In this study, we have used this cell model to identify cis-acting elements of the LHbeta gene that mediate stimulation by GnRH. Analysis of a series of 5'-deletion and internal deletion constructs has revealed two regions of the rat LHbeta gene promoter involved in mediating the response to GnRH, region A (-490/-352) and region B (-207/-82). Fusion of region A upstream of a heterologous minimal promoter linked to the luciferase gene conferred GnRH responsiveness to the promoter, whereas region B did not. However, the presence of both regions A and B conferred a greater GnRH response than region A alone. Electrophoretic mobility shift assay revealed the presence of a protein(s) binding to region A using GH3 as well as alphaT3-1 nuclear extracts. Thus, region A (-490/-352) confers GnRH responsiveness to the LHbeta subunit gene and binds to a protein(s) present in pituitary cell lines. DNA sequences in region B (-207/-82) also contribute to GnRH responsiveness. The identification of putative GnRH response elements in the rat LHbeta gene promoter will aid in elucidation of the mechanisms of regulation of gene expression by GnRH.
促性腺激素释放激素(GnRH)通过调节垂体促性腺激素LH和FSH的生物合成及分泌,在生殖发育和功能中发挥关键作用。尽管已知GnRH可诱导促性腺激素亚基基因转录,但其发生机制尚未阐明。由于缺乏表达LH和FSH亚基基因并对GnRH有反应的可用细胞系,相关研究受到阻碍。我们已用大鼠GnRH受体互补DNA转染大鼠垂体GH3细胞系。当这些细胞与融合了荧光素酶报告基因的LH或FSH亚基基因的调控区共转染时,对GnRH的反应是启动子活性增加,与原代大鼠垂体细胞中的情况相当。在本研究中,我们利用该细胞模型鉴定介导GnRH刺激的LHβ基因的顺式作用元件。对一系列5'-缺失和内部缺失构建体的分析揭示了大鼠LHβ基因启动子中参与介导对GnRH反应的两个区域,区域A(-490 / -352)和区域B(-207 / -82)。将区域A融合到与荧光素酶基因相连的异源最小启动子上游,赋予启动子对GnRH的反应性,而区域B则没有。然而,区域A和B同时存在时赋予的GnRH反应比单独的区域A更大。电泳迁移率变动分析显示,使用GH3以及αT3-1细胞核提取物时存在与区域A结合的一种或多种蛋白质。因此,区域A(-490 / -352)赋予LHβ亚基基因对GnRH的反应性,并与垂体细胞系中存在的一种或多种蛋白质结合。区域B(-207 / -82)中的DNA序列也有助于GnRH反应性。鉴定大鼠LHβ基因启动子中假定的GnRH反应元件将有助于阐明GnRH对基因表达的调控机制。