Tu A S, Patterson D
J Cell Physiol. 1978 Jul;96(1):123-32. doi: 10.1002/jcp.1040960115.
A contingent auxotrophic mutant of CHO-Kl cell is described. This mutant grows in minimal medium. Its growth is inhibited by the exogenous addition of guanine at levels which do not affect the wild type parent. Adenine reverses the guanine effect. This mutant does not complement ade-H (defective in adenylosuccinate synthetase) and has been denoted as ade-HG because of its guanine sensitivity. Some partial revertants of ade-H are found to be also sensitive to guanine, suggesting a close relationship between the ade-H locus and the guanine sensitivity. Studies of 14C-hypoxanthine incorporation into nucleotides indicated that ade-HG has some adenylosuccinate synthetase activity whether it is pre-exposed to guanine or not. Early de novo purine synthesis in ade-HG, however, is greatly inhibited when pre-exposed to guanine. This inhibition of purine synthesis by guanine is reversible and its recovery is facilitated by adenine.
描述了一种CHO-K1细胞的条件营养缺陷型突变体。该突变体在基本培养基中生长。外源添加鸟嘌呤会抑制其生长,而相同水平的鸟嘌呤对野生型亲本无影响。腺嘌呤可逆转鸟嘌呤的这种作用。该突变体不能与ade-H(腺苷酸琥珀酸合成酶缺陷)互补,因其对鸟嘌呤敏感,故被命名为ade-HG。发现ade-H的一些部分回复突变体也对鸟嘌呤敏感,这表明ade-H位点与鸟嘌呤敏感性之间存在密切关系。对14C-次黄嘌呤掺入核苷酸的研究表明,无论是否预先暴露于鸟嘌呤,ade-HG都具有一定的腺苷酸琥珀酸合成酶活性。然而,当预先暴露于鸟嘌呤时,ade-HG中的早期嘌呤从头合成会受到极大抑制。鸟嘌呤对嘌呤合成的这种抑制作用是可逆的,腺嘌呤可促进其恢复。