Huang K N, Symington L S
Institute of Cancer Research, Columbia University College of Physicians and Surgeons, New York, New York 10032.
Mol Cell Biol. 1994 Sep;14(9):6039-45. doi: 10.1128/mcb.14.9.6039-6045.1994.
We have isolated a recessive allele of the yeast protein kinase C gene (PKC1) which promotes an elevated rate of mitotic recombination and confers a temperature-sensitive growth defect. The rate of recombination was increased between genes in direct repeat and at a series of heteroalleles and was dependent upon the RAD52 gene product. The mutant pkc1 allele was sequenced and found to encode a single amino acid change within the catalytic domain. Osmotic stabilizing agents rescued the temperature-sensitive growth defect but not the hyperrecombination phenotype, indicating that the two traits are separable. This separability suggests that the PKC1 gene product (Pkc1p) regulates DNA metabolism by an alternate pathway to that used in the regulation of cell lysis. The regulation of recombination is a previously unidentified role for Pkc1p.
我们分离出了酵母蛋白激酶C基因(PKC1)的一个隐性等位基因,该基因促进有丝分裂重组速率升高,并导致温度敏感型生长缺陷。直接重复基因间以及一系列异等位基因间的重组速率均增加,且依赖于RAD52基因产物。对突变的pkc1等位基因进行测序,发现其在催化结构域内编码一个单一氨基酸变化。渗透稳定剂可挽救温度敏感型生长缺陷,但不能挽救高重组表型,这表明这两个性状是可分离的。这种可分离性表明,PKC1基因产物(Pkc1p)通过一条不同于用于调节细胞裂解的途径来调节DNA代谢。重组调控是Pkc1p以前未被识别的作用。