Coffino P, Bourne H R, Tomkins G M
J Cell Physiol. 1975 Jun;85(3):603-10. doi: 10.1002/jcp.1040850312.
Dibutyryl cyclic AMP and theophylline kill S49.1 mouse lymphoma tissue culture cells. When cells are grown in soft agar with these drugs, the few clones that survive are resistant to cytolysis. The rate of mutation to resistance is 1-3 times 10-7/cell/generation in both diploid and tetraploid cells. The incidence of mutants is increased by treatment with a chemical mutagen, ICR 191. The mutation is consistently associated with greatly reduced or absent cytoplasmic cyclic AMP binding protein. These results suggest that a somatic mutation leads to a defect of the protein kinase regulatory subunit and that activity of this kinase is required for induction of cell death by cyclic AMP.
二丁酰环磷酸腺苷(Dibutyryl cyclic AMP)和茶碱可杀死S49.1小鼠淋巴瘤组织培养细胞。当细胞在含有这些药物的软琼脂中生长时,少数存活的克隆对细胞溶解具有抗性。二倍体细胞和四倍体细胞中对药物产生抗性的突变率均为1 - 3×10⁻⁷/细胞/代。用化学诱变剂ICR 191处理可增加突变体的发生率。这种突变始终与细胞质环磷酸腺苷结合蛋白大量减少或缺失有关。这些结果表明,体细胞突变导致蛋白激酶调节亚基出现缺陷,并且这种激酶的活性是环磷酸腺苷诱导细胞死亡所必需的。