Lemaire I, Coffino P
Cell. 1977 May;11(1):149-55. doi: 10.1016/0092-8674(77)90325-7.
Wild-type S49 lymphoma cells respond to cyclic adenosine 3', 5'-monophosphate (cAMP) by inducing cAMP phosphodiesterase, halting growth in the G1 phase of the cell cycle and subsequently dying. By using a counter selection procedure, we have isolated a new class of mutants of S49 cells termed "deathless" that are resistant to cytolysis, but otherwise respond like the wild-type cells to cAMP. Upon removal of the cyclic nucleotide, D-cells resume their normal growth. Unlike all other cAMP-resistant mutants of S49 cells isolated until now, the D- mutant has a functionally normal cAMP-dependent protein kinase and retains normal ability to induce phosphodiesterase and arrest cell growth in G1. It is probable that the altered gene product of the D- mutant is distal to protein kinase and in a biochemical pathway separate from that of cAMP induction of phosphodiesterase or growth arrest. The D- mutant may facilitate studies of the mechanism of cAMP-induced cytolysis and growth regulation in S49 cells.
野生型S49淋巴瘤细胞通过诱导环磷酸腺苷(cAMP)磷酸二酯酶来响应cAMP,在细胞周期的G1期停止生长并随后死亡。通过使用反选择程序,我们分离出了一类新的S49细胞突变体,称为“不死的”,它们对细胞溶解具有抗性,但在其他方面对cAMP的反应与野生型细胞相似。去除环核苷酸后,D细胞恢复正常生长。与迄今为止分离出的所有其他抗cAMP的S49细胞突变体不同,D突变体具有功能正常的cAMP依赖性蛋白激酶,并保留了诱导磷酸二酯酶和使细胞在G1期停止生长的正常能力。D突变体改变的基因产物可能位于蛋白激酶的下游,并且处于与cAMP诱导磷酸二酯酶或生长停滞的生化途径不同的途径中。D突变体可能有助于研究S49细胞中cAMP诱导的细胞溶解和生长调节机制。