Mitsuzawa H
Institute of Molecular and Cellular Biosciences, University of Tokyo, Japan.
Genetics. 1993 Oct;135(2):321-6. doi: 10.1093/genetics/135.2.321.
The Saccharomyces cerevisiae strain P-28-24C, from which cAMP requiring mutants derived, responded to exogenously added cAMP. Upon the addition of cAMP, this strain showed phenotypes shared by mutants with elevated activity of the cAMP pathway. Genetic analysis involving serial crosses of this strain to a strain with another genetic background revealed that the responsiveness to cAMP results from naturally occurring loss-of-function alleles of PDE1 and PDE2, which encode low and high affinity cAMP phosphodiesterases, respectively. In addition, P-28-24C was found to carry a mutation conferring slow growth that lies in CYR1, which encodes adenylate cyclase, and the slow growth phenotype caused by the cyr1 mutation was suppressed by the pde2 mutation. Therefore P-28-24C is fortuitously a pde1 pde2 cyr1 triple mutant. Responsiveness to cAMP conferred by pde mutations suggests that S. cerevisiae cells are permeable to cAMP to some extent and that the apparent absence of effect of exogenously added cAMP on wild-type cells is due to immediate degradation by cAMP phosphodiesterases.
酿酒酵母菌株P - 28 - 24C可产生需要cAMP的突变体,它对外源添加的cAMP有反应。添加cAMP后,该菌株表现出与cAMP途径活性升高的突变体共有的表型。对该菌株与另一个具有不同遗传背景的菌株进行系列杂交的遗传分析表明,对cAMP的反应性是由PDE1和PDE2的自然发生的功能丧失等位基因引起的,它们分别编码低亲和力和高亲和力的cAMP磷酸二酯酶。此外,发现P - 28 - 24C在编码腺苷酸环化酶的CYR1中携带一个导致生长缓慢的突变,并且由cyr1突变引起的生长缓慢表型被pde2突变所抑制。因此,P - 28 - 24C偶然地是一个pde1 pde2 cyr1三重突变体。pde突变赋予的对cAMP的反应性表明,酿酒酵母细胞在一定程度上对cAMP是可渗透的,并且外源添加的cAMP对野生型细胞明显没有影响是由于被cAMP磷酸二酯酶立即降解。