Kumar T R, Fairchild-Huntress V, Low M J
Vollum Institute for Advanced Biomedical Research, Department of Biochemistry and Molecular Biology, Oregon Health Sciences University, Portland 97201-3098.
Mol Endocrinol. 1992 Jan;6(1):81-90. doi: 10.1210/mend.6.1.1738375.
The molecular basis for the cell-specific and hormonal regulation of the pituitary gonadotropin beta-subunit genes is unknown. To identify the essential DNA regulatory elements of the human FSH beta (hFSH beta) gene, we introduced a 10-kilobase cloned fragment encompassing the gene into the germline of transgenic mice. We showed by a combination of Northern blot hybridization, RIA, and immunofluorescence histochemistry that the hFSH beta gene was expressed exclusively in mouse pituitary gonadotropes. Human FSH beta was actively secreted, presumably as an interspecies heterodimer, with mouse alpha-subunit, and no free hFSH beta was detected in serum. Male transgenic mice consistently had higher basal pituitary expression and secretion of hFSH beta than the female transgenic mice. Castration combined with testosterone replacement caused a marked reduction in hFSH beta gene expression in transgenic males, but had no effect on the pituitary levels of FSH in normal male mice. These experiments demonstrate that the essential DNA regulatory elements and gonadotrope transcription factors required for cell-specific expression of the FSH beta gene must be conserved between human and mouse. There appear to be important differences in the hormonal regulation of the gene between species, however.
垂体促性腺激素β亚基基因的细胞特异性和激素调节的分子基础尚不清楚。为了鉴定人类促卵泡激素β(hFSHβ)基因的必需DNA调控元件,我们将包含该基因的10千碱基克隆片段导入转基因小鼠的种系。通过Northern印迹杂交、放射免疫分析和免疫荧光组织化学相结合的方法,我们发现hFSHβ基因仅在小鼠垂体促性腺细胞中表达。人FSHβ被主动分泌,推测是以种间异源二聚体的形式与小鼠α亚基结合,并且在血清中未检测到游离的hFSHβ。雄性转基因小鼠的垂体hFSHβ基础表达和分泌水平始终高于雌性转基因小鼠。去势联合睾酮替代导致转基因雄性小鼠中hFSHβ基因表达显著降低,但对正常雄性小鼠垂体中的FSH水平没有影响。这些实验表明,FSHβ基因细胞特异性表达所需的必需DNA调控元件和促性腺细胞转录因子在人和小鼠之间一定是保守的。然而,不同物种之间该基因的激素调节似乎存在重要差异。