Dobner P R, Kawasaki E S, Yu L Y, Bancroft F C
Proc Natl Acad Sci U S A. 1981 Apr;78(4):2230-4. doi: 10.1073/pnas.78.4.2230.
Thyroid or glucocorticoid hormone increases the synthesis of growth hormone (GH) by clonal lines of rat pituitary tumor cells. To investigate whether these increases arise from increased accumulation of GH-specific RNA sequences in the cytoplasm and nuclei of these cells, we adapted two existing procedures so that a 32P-labeled hybrid plasmid containing a cDNA sequence could be used to quantitate relative concentrations of the corresponding mRNA. One method (RNA gel blot hybridization) used electrophoresis of RNA, transfer to nitrocellulose paper, and hybridization to 32P-labeled plasmid. The other (RNA dot hybridization) used covalent attachment of RNA to activated cellulose paper squares and hybridization to 32P-labeled plasmid. As probe, we used a hybrid plasmid (pBR322-GH1) which we show by restriction analysis to contain a DNA sequence coding for rat GH. The results were comparable from both techniques and showed that incubation of GH3 cells with a thyroid hormone (triiodothyronine), a glucocorticoid hormone (dexamethasone), or both hormones caused an increase of cytoplasmic pre-GH mRNA sequences of about 4-, 22-, and 13-fold, respectively. Results obtained with the RNA gel blot hybridization method showed that hormonal stimulation leads to the induction of a single 1.0-kilobase species of pre-GH mRNA in the cytoplasm and of 2.7- and 1.0- kilobase species of GH-specific RNA in the nucleus.
甲状腺激素或糖皮质激素可增加大鼠垂体肿瘤细胞克隆系中生长激素(GH)的合成。为了研究这些增加是否源于这些细胞的细胞质和细胞核中GH特异性RNA序列的积累增加,我们对两种现有方法进行了改进,以便使用含有cDNA序列的32P标记杂交质粒来定量相应mRNA的相对浓度。一种方法(RNA凝胶印迹杂交)是对RNA进行电泳,转移到硝酸纤维素纸上,然后与32P标记的质粒杂交。另一种方法(RNA斑点杂交)是将RNA共价连接到活化的纤维素纸片上,然后与32P标记的质粒杂交。作为探针,我们使用了一种杂交质粒(pBR322-GH1),通过限制性分析表明其含有编码大鼠GH的DNA序列。两种技术的结果相当,表明用甲状腺激素(三碘甲状腺原氨酸)、糖皮质激素(地塞米松)或两种激素孵育GH3细胞,分别导致细胞质中前GH mRNA序列增加约4倍、22倍和13倍。用RNA凝胶印迹杂交法获得的结果表明,激素刺激导致细胞质中诱导出一种单一的1.0千碱基的前GH mRNA,以及细胞核中2.7千碱基和1.0千碱基的GH特异性RNA。