Casperson G F, Walker N, Bourne H R
Proc Natl Acad Sci U S A. 1985 Aug;82(15):5060-3. doi: 10.1073/pnas.82.15.5060.
By complementation of the cyr1-1 mutation in Saccharomyces cerevisiae, we have isolated yeast genomic DNA containing the structural gene that encodes the catalytic unit of adenylate cyclase (EC 4.6.1.1). The isolated DNA restored adenylate cyclase activity to cyr1-1 mutants and directed integration at the CYR1 locus. Wild-type strains transformed with CYR1 DNA on the high copy number vector YEp24 contained 4- to 6-fold more adenylate cyclase activity than strains carrying the plasmid with no insert. This result suggests that expression of the CYR1 gene product, rather than that of other polypeptide components of the adenylate cyclase system, limits total adenylate cyclase activity in S. cerevisiae. CYR1-containing plasmids also complemented the temperature-sensitive growth defect of the cell division cycle mutation cdc35-1, which confers a phenotype under restrictive conditions similar to that of cyr1-1 and maps to the same locus. Further, cdc35-1 cam mutants, which contain mutations that enable them to take up cAMP from the medium, grew at the restrictive temperature in the presence of exogenous cAMP. These observations support the view that CDC35 and CYR1 are allelic and confirm the hypothesis that cAMP synthesis is required for cells to pass through the "start" position of the cell division cycle.
通过对酿酒酵母中cyr1-1突变进行互补,我们分离出了含有编码腺苷酸环化酶(EC 4.6.1.1)催化单元结构基因的酵母基因组DNA。分离出的DNA将腺苷酸环化酶活性恢复到cyr1-1突变体中,并指导其在CYR1基因座处整合。用高拷贝数载体YEp24上的CYR1 DNA转化的野生型菌株,其腺苷酸环化酶活性比携带无插入片段质粒的菌株高4至6倍。这一结果表明,CYR1基因产物的表达而非腺苷酸环化酶系统其他多肽成分的表达,限制了酿酒酵母中总的腺苷酸环化酶活性。含有CYR1的质粒也互补了细胞分裂周期突变cdc35-1的温度敏感型生长缺陷,该突变在限制条件下赋予的表型与cyr1-1相似,且定位于同一基因座。此外,含有能使其从培养基中摄取cAMP的突变的cdc35-1 cam突变体,在存在外源cAMP的情况下于限制温度下生长。这些观察结果支持了CDC35和CYR1是等位基因的观点,并证实了细胞通过细胞分裂周期的“起始”位置需要cAMP合成的假说。