White-Ziegler Christine A, Um Suzin, Pérez Natalie M, Berns Abby L, Malhowski Amy J, Young Sarah
Department of Biological Sciences and Program in Biochemistry, Smith College, Northampton, MA 01063, USA.
Microbiology (Reading). 2008 Jan;154(Pt 1):148-166. doi: 10.1099/mic.0.2007/012021-0.
Temperature serves as a cue to regulate gene expression in Escherichia coli and other bacteria. Using DNA microarrays, we identified 297 genes whose expression is increased at 23 degrees C compared to 37 degrees C in E. coli K-12. Of these genes, 122 are RpoS-controlled, confirming genome-wide the model that low temperature serves as a primary cue to trigger the general stress response. Several genes expressed at 23 degrees C overlap with the cold-shock response, suggesting that strategies used to adapt to sudden shifts in temperature also mediate long-term growth at 23 degrees C. Another category of genes more highly expressed at 23 degrees C are associated with biofilm development, implicating temperature as an important cue influencing this developmental pathway. In a candidate set of genes tested, the biofilm genes (adrA, bolA, mlrA, nhaR, csgA, yceP/bssS) and cold-shock genes (otsA, yceP/bssS) were found to be RpoS- and DsrA-dependent for their transcription at 23 degrees C. In contrast, transcription of three genes (ycgZ, dps and ymgB) was either partially or fully independent of these regulators, signifying there is an alternative thermoregulatory mechanism(s) that increases gene expression at 23 degrees C. Increased expression at 23 degrees C compared to 37 degrees C is retained in various media tested for most of the genes, supporting the relative importance of this cue in adaptation to changing environments. Both the RpoS-dependent gene otsA and the RpoS-independent gene ymgB demonstrated increased expression levels within 1 h after a shift from 37 to 23 degrees C, indicating a rapid response to this environmental cue. Despite changes in gene expression for many RpoS-dependent genes, experiments assessing growth rate at 23 degrees C and viability at 4 degrees C did not demonstrate significant impairment in rpoS : : Tn10 or dsrA : : cat mutant strains in comparison to the wild-type strain. Biofilm formation was favoured at low temperature and is moderately impaired in both the rpoS : : Tn10 and dsrA : : cat mutants at 23 degrees C, suggesting genes controlled by these regulators play a role necessary for optimal biofilm formation at 23 degrees C. Taken together, our data demonstrate that a large number of genes are increased in expression at 23 degrees C to globally respond to this environmental change and that at least two thermoregulatory pathways are involved in co-ordinating this response - the RpoS/DsrA pathway and an alternative thermoregulatory pathway, independent of these regulators.
温度是调节大肠杆菌及其他细菌基因表达的一个信号。我们利用DNA微阵列,在大肠杆菌K-12中鉴定出297个基因,其在23℃时的表达相较于37℃有所增加。在这些基因中,有122个受RpoS调控,从全基因组范围证实了低温作为触发一般应激反应的主要信号这一模型。一些在23℃表达的基因与冷休克反应重叠,这表明用于适应温度突然变化的策略也介导了在23℃的长期生长。另一类在23℃时表达更高的基因与生物膜形成相关,这意味着温度是影响这一发育途径的重要信号。在所测试的一组候选基因中,发现生物膜基因(adrA、bolA、mlrA、nhaR、csgA、yceP/bssS)和冷休克基因(otsA、yceP/bssS)在23℃时的转录依赖于RpoS和DsrA。相比之下,三个基因(ycgZ、dps和ymgB)的转录部分或完全独立于这些调节因子,这表明存在一种替代的温度调节机制,可在23℃时增加基因表达。在测试的各种培养基中,大多数基因在23℃时相较于37℃表达增加,这支持了该信号在适应变化环境中的相对重要性。依赖RpoS的基因otsA和不依赖RpoS的基因ymgB在从37℃转变到23℃后的1小时内表达水平均升高,表明对这一环境信号有快速反应。尽管许多依赖RpoS的基因发生了表达变化,但评估23℃生长速率和4℃生存能力的实验表明,与野生型菌株相比,rpoS::Tn10或dsrA::cat突变菌株并未表现出明显的损伤。低温有利于生物膜形成,在23℃时,rpoS::Tn10和dsrA::cat突变体的生物膜形成均受到一定程度的损害,这表明这些调节因子控制的基因在23℃时对最佳生物膜形成起着必要作用。综上所述,我们的数据表明,大量基因在23℃时表达增加以全局响应这一环境变化,并且至少有两条温度调节途径参与协调这一反应——RpoS/DsrA途径和一条独立于这些调节因子的替代温度调节途径。