Division of Endodontology, Department of Conservative Dentistry, Showa University School of Dentistry, Tokyo, Japan.
Department of Oral Microbiology and Immunology, Showa University School of Dentistry, Tokyo, Japan
Infect Immun. 2018 Feb 20;86(3). doi: 10.1128/IAI.00894-17. Print 2018 Mar.
Small noncoding RNAs (sRNAs) have been identified as important regulators of gene expression in various cellular processes. -dependent small RNAs (csRNAs), a group of sRNAs that are controlled by the two-component regulatory system CiaRH, are widely conserved in streptococci, but their targets have been identified only in , a pioneer colonizer of teeth and one of the most predominant bacteria in the early oral biofilm, has been shown to have six csRNAs. Using computational target prediction and the luciferase reporter assay, we identified , a constituent of the type IV pilus operon, as a negative regulatory target for one of the csRNAs, namely, csRNA1-1, in RNA-RNA electrophoretic mobility shift assay using a nucleotide exchange mutant of csRNA1-1 revealed that csRNA1-1 binds directly to mRNA. In addition, csRNA1-1 and csRNA1-2, a putative gene duplication product of csRNA1-1 that is tandemly located in the genome, negatively regulated biofilm formation. These results suggest the involvement of csRNAs in the colonization step of .
小型非编码 RNA(sRNAs)已被鉴定为各种细胞过程中基因表达的重要调节剂。依赖于双组分调节系统 CiaRH 的调控的小 RNA(csRNAs)是一组在链球菌中广泛保守的 sRNAs,但它们的靶标仅在 中被鉴定,这是一种牙定植的先驱者,也是早期口腔生物膜中最主要的细菌之一,已被证明有六个 csRNAs。使用计算靶标预测和荧光素酶报告基因检测,我们鉴定了 ,一种 IV 型菌毛操纵子的组成部分,作为一种 csRNA(即 csRNA1-1)的负调节靶标,在使用 csRNA1-1 的核苷酸交换突变体的 RNA-RNA 电泳迁移率变动测定中,csRNA1-1 与 mRNA 直接结合。此外,csRNA1-1 和 csRNA1-2,csRNA1-1 的推定基因重复产物,串联位于 基因组中,负调节 生物膜形成。这些结果表明 csRNAs 参与了 的定植步骤。