Murli S, Opperman T, Smith B T, Walker G C
Department of Biology, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139, USA.
J Bacteriol. 2000 Feb;182(4):1127-35. doi: 10.1128/JB.182.4.1127-1135.2000.
The umuDC gene products, whose expression is induced by DNA-damaging treatments, have been extensively characterized for their role in SOS mutagenesis. We have recently presented evidence that supports a role for the umuDC gene products in the regulation of growth after DNA damage in exponentially growing cells, analogous to a prokaryotic DNA damage checkpoint. Our further characterization of the growth inhibition at 30 degrees C associated with constitutive expression of the umuDC gene products from a multicopy plasmid has shown that the umuDC gene products specifically inhibit the transition from stationary phase to exponential growth at the restrictive temperature of 30 degrees C and that this is correlated with a rapid inhibition of DNA synthesis. These observations led to the finding that physiologically relevant levels of the umuDC gene products, expressed from a single, SOS-regulated chromosomal copy of the operon, modulate the transition to rapid growth in E. coli cells that have experienced DNA damage while in stationary phase. This activity of the umuDC gene products is correlated with an increase in survival after UV irradiation. In a distinction from SOS mutagenesis, uncleaved UmuD together with UmuC is responsible for this activity. The umuDC-dependent increase in resistance in UV-irradiated stationary-phase cells appears to involve, at least in part, counteracting a Fis-dependent activity and thereby regulating the transition to rapid growth in cells that have experienced DNA damage. Thus, the umuDC gene products appear to increase DNA damage tolerance at least partially by regulating growth after DNA damage in both exponentially growing and stationary-phase cells.
umuDC基因产物的表达可由DNA损伤处理诱导,其在SOS诱变中的作用已得到广泛研究。我们最近提供的证据支持umuDC基因产物在指数生长细胞DNA损伤后的生长调控中发挥作用,类似于原核生物的DNA损伤检查点。我们对多拷贝质粒组成型表达umuDC基因产物所导致的30℃生长抑制的进一步研究表明,umuDC基因产物在30℃的限制温度下特异性抑制从稳定期到指数生长期的转变,且这与DNA合成的快速抑制相关。这些观察结果导致发现,从操纵子的单个SOS调控染色体拷贝表达的生理相关水平的umuDC基因产物,可调节处于稳定期时经历过DNA损伤的大肠杆菌细胞向快速生长的转变。umuDC基因产物的这种活性与紫外线照射后存活率的提高相关。与SOS诱变不同的是,未切割的UmuD与UmuC共同负责这种活性。紫外线照射的稳定期细胞中umuDC依赖性抗性的增加似乎至少部分涉及抵消Fis依赖性活性,从而调节经历过DNA损伤的细胞向快速生长的转变。因此,umuDC基因产物似乎至少部分通过调节指数生长和稳定期细胞DNA损伤后的生长来提高DNA损伤耐受性。