Department of Biology, Indiana University-Bloomington, Bloomington, IN 47405, USA.
J Bacteriol. 2010 Jan;192(1):264-79. doi: 10.1128/JB.01204-09.
We report a search for small RNAs (sRNAs) in the low-GC, gram-positive human pathogen Streptococcus pneumoniae. Based on bioinformatic analyses by Livny et al. (J. Livny, A. Brencic, S. Lory, and M. K. Waldor, Nucleic Acids Res. 34:3484-3493, 2006), we tested 40 candidates by Northern blotting and confirmed the expression of nine new and one previously reported (CcnA) sRNAs in strain D39. CcnA is one of five redundant sRNAs reported by Halfmann et al. (A. Halfmann, M. Kovacs, R. Hakenbeck, and R. Bruckner, Mol. Microbiol. 66:110-126, 2007) that are positively controlled by the CiaR response regulator. We characterized 3 of these 14 sRNAs: Spd-sr17 (144 nucleotides [nt]; decreased in stationary phase), Spd-sr37 (80 nt; strongly expressed in all growth phases), and CcnA (93 nt; induced by competence stimulatory peptide). Spd-sr17 and CcnA likely fold into structures containing single-stranded regions between hairpin structures, whereas Spd-sr37 forms a base-paired structure. Primer extension mapping and ectopic expression in deletion/insertion mutants confirmed the independent expression of the three sRNAs. Microarray analyses indicated that insertion/deletion mutants in spd-sr37 and ccnA exerted strong cis-acting effects on the transcription of adjacent genes, indicating that these sRNA regions are also cotranscribed in operons. Deletion or overexpression of the three sRNAs did not cause changes in growth, certain stress responses, global transcription, or virulence. Constitutive ectopic expression of CcnA reversed some phenotypes of D39 Delta ciaR mutants, but attempts to link CcnA to -E to comC as a target were inconclusive in ciaR(+) strains. These results show that S. pneumoniae, which lacks known RNA chaperones, expresses numerous sRNAs, but three of these sRNAs do not strongly affect common phenotypes or transcription patterns.
我们报告了在低 GC 革兰阳性人类病原体肺炎链球菌中寻找小 RNA (sRNA) 的研究。基于 Livny 等人的生物信息学分析(J. Livny、A. Brencic、S. Lory 和 M. K. Waldor,Nucleic Acids Res. 34:3484-3493, 2006),我们通过 Northern 印迹测试了 40 个候选物,并在 D39 株中证实了 9 个新的和 1 个先前报道的(CcnA)sRNA 的表达。CcnA 是 Halfmann 等人报道的五个冗余 sRNA 之一(A. Halfmann、M. Kovacs、R. Hakenbeck 和 R. Bruckner,Mol. Microbiol. 66:110-126, 2007),它们受 CiaR 反应调节剂的正调控。我们对这 14 个 sRNA 中的 3 个进行了表征:Spd-sr17(144 个核苷酸 [nt];在静止期减少)、Spd-sr37(80 nt;在所有生长阶段都强烈表达)和 CcnA(93 nt;由竞争刺激肽诱导)。Spd-sr17 和 CcnA 可能折叠成发夹结构之间含有单链区域的结构,而 Spd-sr37 形成碱基配对结构。引物延伸作图和缺失/插入突变体中的异位表达证实了这三个 sRNA 的独立表达。微阵列分析表明,spd-sr37 和 ccnA 缺失/插入突变体对相邻基因的转录具有强烈的顺式作用效应,表明这些 sRNA 区域也在操纵子中共转录。三个 sRNA 的缺失或过表达不会导致生长、某些应激反应、全局转录或毒力的变化。CcnA 的组成型异位表达逆转了 D39 Delta ciaR 突变体的一些表型,但在 ciaR(+) 菌株中,试图将 CcnA 与-E 连接到 comC 作为靶标尚无定论。这些结果表明,缺乏已知 RNA 伴侣的肺炎链球菌表达了许多 sRNA,但其中三个 sRNA 不会强烈影响常见表型或转录模式。