Johnson A L, Barker D G, Johnston L H
Laboratory of Cell Propagation, National Institute for Medical Research, Mill Hill, London, UK.
Curr Genet. 1986;11(2):107-12. doi: 10.1007/BF00378201.
UV-irradiation of stationary phase cells of Saccharomyces cerevisiae and Schizosaccharomyces pombe leads to a 9-fold and 90-fold increase in transcript levels from the respective DNA ligase genes CDC9 and CDC17, whereas exponential cells show only 3-fold and 2-fold increases. Induction of CDC9 after MMS treatment and gamma-irradiation was also observed by using a CDC9-lacZ translational fusion and assaying for beta-galactosidase. Surprisingly, irradiation of S. cerevisiae induces only a 50% increase in DNA ligase itself, probably reflecting the extremely high in vivo stability of the enzyme. The UV-induction of ligase may be part of a "fail-safe" mechanism which, together with the enzyme stability, ensures adequate supplies of this essential enzyme.
对酿酒酵母和粟酒裂殖酵母的静止期细胞进行紫外线照射,会使各自的DNA连接酶基因CDC9和CDC17的转录水平分别提高9倍和90倍,而对数期细胞仅显示3倍和2倍的增加。通过使用CDC9-lacZ翻译融合体并检测β-半乳糖苷酶,还观察到了MMS处理和γ射线照射后CDC9的诱导情况。令人惊讶的是,酿酒酵母的照射仅使DNA连接酶本身增加50%,这可能反映了该酶在体内极高的稳定性。连接酶的紫外线诱导可能是“故障安全”机制的一部分,该机制与酶的稳定性一起,确保了这种必需酶的充足供应。