Mason A J, Pitts S L, Nikolics K, Szonyi E, Wilcox J N, Seeburg P H, Stewart T A
Science. 1986 Dec 12;234(4782):1372-8. doi: 10.1126/science.3097822.
The hypogonadal (hpg) mouse lacks a complete gonadotropin-releasing hormone (GnRH) gene and consequently cannot reproduce. Introduction of an intact GnRH gene into the genome of these mutant mice resulted in complete reversal of the hypogonadal phenotype. Transgenic hpg/hpg homozygotes of both sexes were capable of mating and producing offspring. Pituitary and serum concentrations of luteinizing hormone, follicle-stimulating hormone, and prolactin were restored to those of normal animals. Immunocytochemistry and in situ hybridization showed that GnRH expression was restored in the appropriate hypothalamic neurons of the transgenic hpg animals, an indication of neural-specific expression of the introduced gene.
性腺功能减退(hpg)小鼠缺乏完整的促性腺激素释放激素(GnRH)基因,因此无法繁殖。将完整的GnRH基因导入这些突变小鼠的基因组后,性腺功能减退的表型完全逆转。两性转基因hpg/hpg纯合子都能够交配并产生后代。垂体和血清中促黄体生成素、促卵泡激素和催乳素的浓度恢复到正常动物的水平。免疫细胞化学和原位杂交显示,转基因hpg动物下丘脑的适当神经元中恢复了GnRH表达,这表明导入基因的神经特异性表达。