Diallo Idrissa, Ho Jeffrey, Lalaouna David, Massé Eric, Provost Patrick
CHU de Québec Research Center/CHUL Pavilion, Department of Microbiology, Infectious Diseases and Immunology, Faculty of Medicine, Université Laval, Quebec City, QC, Canada.
CRCHUS, RNA Group, Department of Biochemistry and Functional Genomics, Faculty of Medicine and Health Sciences, Université de Sherbrooke, Sherbrooke, QC, Canada.
Front Mol Biosci. 2022 Jun 3;9:914991. doi: 10.3389/fmolb.2022.914991. eCollection 2022.
RNA sequencing (RNA-seq) is the gold standard for the discovery of small non-coding RNAs. Following a long-standing approach, reads shorter than 16 nucleotides (nt) are removed from the small RNA sequencing libraries or datasets. The serendipitous discovery of an eukaryotic 12 nt-long RNA species capable of modulating the microRNA from which they derive prompted us to challenge this dogma and, by expanding the window of RNA sizes down to 8 nt, to confirm the existence of functional very small RNAs (vsRNAs <16 nt). Here we report the detailed profiling of vsRNAs in , -derived outer membrane vesicles (OMVs) and five other bacterial strains ( PA7, PAO1, serovar Typhimurium 14028S, JR32 Philadelphia-1 and HG001). vsRNAs of 8-15 nt in length [RNAs (8-15 nt)] were found to be more abundant than RNAs of 16-30 nt in length [RNAs (16-30 nt)]. vsRNA biotypes were distinct and varied within and across bacterial species and accounted for one third of reads identified in the 8-30 nt window. The tRNA-derived fragments (tRFs) have appeared as a major biotype among the vsRNAs, notably Ile-tRF and Ala-tRF, and were selectively loaded in OMVs. tRF-derived vsRNAs appear to be thermodynamically stable with at least 2 G-C basepairs and stem-loop structure. The analyzed tRF-derived vsRNAs are predicted to target several human host mRNAs with diverse functions. Bacterial vsRNAs and OMV-derived vsRNAs could be novel players likely modulating the intricate relationship between pathogens and their hosts.
RNA测序(RNA-seq)是发现小非编码RNA的金标准。按照长期以来的方法,短于16个核苷酸(nt)的读段会从小RNA测序文库或数据集中去除。一种能够调节其来源的微小RNA的真核12 nt长RNA物种的意外发现促使我们挑战这一教条,并通过将RNA大小窗口扩大到8 nt,来确认功能性超小RNA(vsRNAs <16 nt)的存在。在此,我们报告了在 衍生的外膜囊泡(OMV)和其他五种细菌菌株(PA7、PAO1、鼠伤寒沙门氏菌血清型14028S、JR32费城-1和HG001)中vsRNAs的详细图谱分析。发现长度为8 - 15 nt的vsRNAs [RNAs(8 - 15 nt)]比长度为16 - 30 nt的RNAs [RNAs(16 - 30 nt)]更丰富。vsRNA生物型在细菌物种内部和之间是不同且多样的,并且在8 - 30 nt窗口中鉴定出的读段中占三分之一。tRNA衍生片段(tRFs)已成为vsRNAs中的主要生物型,尤其是Ile - tRF和Ala - tRF,并被选择性地装载到OMV中。tRF衍生的vsRNAs似乎具有热力学稳定性,至少有2个G - C碱基对和茎环结构。分析的tRF衍生的vsRNAs预计会靶向几种具有不同功能的人类宿主mRNA。细菌vsRNAs和OMV衍生的vsRNAs可能是调节病原体与其宿主之间复杂关系的新参与者。