Lin C, Lin S C, Chang C P, Rosenfeld M G
Eukaryotic Regulatory Biology Program, University of California, San Diego.
Nature. 1992;360(6406):765-8. doi: 10.1038/360765a0.
In Snell (dw) and Jackson (dwJ) dwarf mice, mutations in the gene encoding Pit-1, a tissue-specific POU-domain transcription factor, lead to the absence of somatotroph, lactotroph and thyrotroph cells. Pre-somatotroph proliferation is stimulated by increased intracellular levels of cyclic AMP, normally induced by growth hormone releasing factor (GRF; refs 7-17). Here we report the cloning of mouse and rat complementary DNAs encoding a new member of the seven-transmembrane-helix, G-protein-coupled receptor family restricted to the pituitary gland, which mediates increases in intracellular cAMP and cAMP-dependent gene transcription in response to GRF. The receptor is expressed in a spatial and temporal pattern corresponding precisely to growth hormone gene expression, and neither is expressed in dw/dw mice. The pituitary hypoplasia in these mice thus appears to be due, at least in part, to the absence of GRF receptor, which is in turn due to the absence of functional Pit-1.
在斯奈尔(dw)和杰克逊(dwJ)侏儒小鼠中,编码垂体特异性POU结构域转录因子Pit-1的基因突变导致生长激素细胞、催乳激素细胞和促甲状腺激素细胞缺失。生长激素释放因子(GRF;参考文献7 - 17)通常会诱导细胞内环磷酸腺苷(cAMP)水平升高,从而刺激前生长激素细胞增殖。在此,我们报告了小鼠和大鼠互补DNA的克隆,这些互补DNA编码一种七跨膜螺旋、G蛋白偶联受体家族的新成员,该受体仅存在于垂体中,它介导细胞内cAMP增加以及cAMP依赖的基因转录以响应GRF。该受体的表达在空间和时间模式上与生长激素基因的表达精确对应,并且在dw/dw小鼠中均不表达。因此,这些小鼠的垂体发育不全似乎至少部分是由于GRF受体缺失所致,而GRF受体缺失又是由于功能性Pit-1缺失所致。