Choi Do-Hee, Oh Young-Mi, Kwon Sung-Hun, Bae Sung-Ho
Department of Biological Sciences, College of Natural Science, Inha University, Incheon 402-751, Republic of Korea.
J Microbiol. 2008 Feb;46(1):75-80. doi: 10.1007/s12275-008-0013-6.
The SRL4 (YPL033C) gene was initially identified by the screening of Saccharomyces cerevisiae genes that play a role in DNA metabolism and/or genome stability using the SOS system of Escherichia coli. In this study, we found that the srl4Delta mutant cells were resistant to the chemicals that inhibit nucleotide metabolism and evidenced higher dNTP levels than were observed in the wild-type cells in the presence of hydroxyurea. The mutant cells also showed a significantly faster growth rate and higher dNTP levels at low temperature (16 degrees C) than were observed in the wild-type cells, whereas we detected no differences in the growth rate at 30 degrees C. Furthermore, srl4Delta was shown to suppress the lethality of mutations of the essential S phase checkpoint genes, RAD53 and LCD1. These results indicate that SRL4 may be involved in the regulation of dNTP production by its function as a negative regulator of ribonucleotide reductase.
SRL4(YPL033C)基因最初是通过使用大肠杆菌的SOS系统筛选在DNA代谢和/或基因组稳定性中起作用的酿酒酵母基因而鉴定出来的。在本研究中,我们发现srl4Delta突变细胞对抑制核苷酸代谢的化学物质具有抗性,并且在存在羟基脲的情况下,其dNTP水平高于野生型细胞。突变细胞在低温(16摄氏度)下也显示出比野生型细胞显著更快的生长速率和更高的dNTP水平,而我们在30摄氏度下未检测到生长速率的差异。此外,srl4Delta被证明可抑制必需的S期检查点基因RAD53和LCD1突变的致死性。这些结果表明,SRL4可能通过作为核糖核苷酸还原酶的负调节因子参与dNTP产生的调节。