Mujahid Sana, Bergholz Teresa M, Oliver Haley F, Boor Kathryn J, Wiedmann Martin
Department of Food Science, Cornell University, Ithaca, NY 14853, USA.
Int J Mol Sci. 2012 Dec 24;14(1):378-93. doi: 10.3390/ijms14010378.
SbrE is a ncRNA in Listeria monocytogenes, reported to be up-regulated by the alternative sigma factor σB. Initial quantitative RT-PCR (qRT-PCR) experiments on parent strains and isogenic ΔsigB strains demonstrated σB-dependent expression of SbrE across the four L. monocytogenes lineages and in L. innocua. Microarray and proteomics (MDLC/MS/MS with iTRAQ labeling) experiments with the L. monocytogenes parent strain and an isogenic ΔsbrE strain identified a single gene (lmo0636) and two proteins (Lmo0637 and Lmo2094) that showed lower expression levels in the ΔsbrE strain. qRT-PCR demonstrated an increase in SbrE transcript levels in stationary phase L. monocytogenes and in bacteria exposed to oxidative stress (mean log2 transcript levels 7.68 ± 0.57 and 1.70 ± 0.71 greater than in mid-log phase cells, respectively). However, no significant differences in growth or survival between the parent strain and ΔsbrE strain were confirmed under a variety of environmental stress conditions tested. Our data suggest that σB-dependent transcription of SbrE represents a conserved mechanism that contributes, across Listeria species, to fine-tuning of gene expression under specific environmental conditions that remain to be defined.
SbrE是单核细胞增生李斯特菌中的一种非编码RNA,据报道它受替代σ因子σB的上调调控。对亲本菌株和同基因ΔsigB菌株进行的初步定量逆转录聚合酶链反应(qRT-PCR)实验表明,在单核细胞增生李斯特菌的四个菌系以及无害李斯特菌中,SbrE的表达依赖于σB。对单核细胞增生李斯特菌亲本菌株和同基因ΔsbrE菌株进行的微阵列和蛋白质组学实验(采用iTRAQ标记的多维液相色谱/串联质谱法)鉴定出一个单一基因(lmo0636)和两种蛋白质(Lmo0637和Lmo2094),它们在ΔsbrE菌株中的表达水平较低。qRT-PCR表明,在单核细胞增生李斯特菌的稳定期以及暴露于氧化应激的细菌中,SbrE转录本水平有所增加(平均log2转录本水平分别比对数中期细胞高7.68±0.57和1.70±0.71)。然而,在测试的各种环境应激条件下,亲本菌株和ΔsbrE菌株之间在生长或存活方面未确认有显著差异。我们的数据表明,SbrE依赖于σB的转录代表一种保守机制,在李斯特菌属中有助于在特定环境条件下对基因表达进行微调,这些特定环境条件尚待确定。