Wong M, O'Brien D, Schimmer B P
Biochem Cell Biol. 1986 Nov;64(11):1066-71. doi: 10.1139/o86-141.
DNA-mediated gene transfer was used to evaluate the cause and effect relationship between mutations in cAMP-dependent protein kinase activity and cellular resistance of adrenocortical tumor cells to ACTH and cAMP. Protein kinase defective, Kin 8 adrenocortical tumor cells were transformed with genomic DNA from an ACTH- and cAMP-responsive adrenocortical cell line and screened for the recovery of morphological responses to the cAMP analog 8-bromo-cAMP (8BrcAMP). 8BrcAMP-responsive transformants were recovered with a frequency of approximately 0.5 per 10(3) transformation-competent cells. These transformants recovered the ability to round up in the presence of ACTH and were able to respond to both ACTH and 8BrcAMP with increased steroidogenesis. They also recovered cAMP-dependent protein kinase activity. The transformants, however, were unstable and concomitantly lost cAMP-dependent protein kinase activity and steroidogenic and morphological responses to ACTH and 8BrcAMP. These observations suggest that a single gene, probably the gene encoding the regulatory subunit of cAMP-dependent protein kinase, is responsible for the resistance of the Kin 8 mutant to ACTH and cAMP.
利用DNA介导的基因转移来评估环磷酸腺苷(cAMP)依赖性蛋白激酶活性突变与肾上腺皮质肿瘤细胞对促肾上腺皮质激素(ACTH)和cAMP的细胞抗性之间的因果关系。用来自ACTH和cAMP反应性肾上腺皮质细胞系的基因组DNA转化蛋白激酶缺陷型的Kin 8肾上腺皮质肿瘤细胞,并筛选对cAMP类似物8-溴-cAMP(8BrcAMP)的形态学反应恢复情况。以约每10³个有转化能力的细胞0.5的频率获得了对8BrcAMP有反应的转化体。这些转化体恢复了在ACTH存在下变圆的能力,并且能够对ACTH和8BrcAMP两者作出反应,从而增加类固醇生成。它们还恢复了cAMP依赖性蛋白激酶活性。然而,这些转化体不稳定,同时失去了cAMP依赖性蛋白激酶活性以及对ACTH和8BrcAMP的类固醇生成和形态学反应。这些观察结果表明,单个基因,可能是编码cAMP依赖性蛋白激酶调节亚基的基因,是Kin 8突变体对ACTH和cAMP产生抗性的原因。