Vaňková Hausnerová Viola, Marvalová Olga, Šiková Michaela, Shoman Mahmoud, Havelková Jarmila, Kambová Milada, Janoušková Martina, Kumar Dilip, Halada Petr, Schwarz Marek, Krásný Libor, Hnilicová Jarmila, Pánek Josef
Laboratory of Microbial Genetics and Gene Expression, Institute of Microbiology of the Czech Academy of Sciences, Prague, Czechia.
Laboratory of Structural Biology and Cell Signaling, Institute of Microbiology of the Czech Academy of Sciences, Vestec, Czechia.
Front Microbiol. 2022 May 11;13:848536. doi: 10.3389/fmicb.2022.848536. eCollection 2022.
Bacteria employ small non-coding RNAs (sRNAs) to regulate gene expression. Ms1 is an sRNA that binds to the RNA polymerase (RNAP) core and affects the intracellular level of this essential enzyme. Ms1 is structurally related to 6S RNA that binds to a different form of RNAP, the holoenzyme bearing the primary sigma factor. 6S RNAs are widespread in the bacterial kingdom except for the industrially and medicinally important . While Ms1 RNA was identified in , it is not clear whether Ms1 RNA is present also in other species. Here, using a computational search based on secondary structure similarities combined with a linguistic gene synteny approach, we identified Ms1 RNA in . In , Ms1 RNA overlaps with the previously annotated scr3559 sRNA with an unknown function. We experimentally confirmed that Ms1 RNA/scr3559 associates with the RNAP core without the primary sigma factor HrdB . Subsequently, we applied the computational approach to other and identified Ms1 RNA candidates in 824 species, revealing Ms1 RNA as a widespread class of RNAP binding sRNAs, and demonstrating the ability of our multifactorial computational approach to identify weakly conserved sRNAs in evolutionarily distant genomes.
细菌利用小非编码RNA(sRNA)来调节基因表达。Ms1是一种与RNA聚合酶(RNAP)核心结合并影响这种必需酶细胞内水平的sRNA。Ms1在结构上与6S RNA相关,6S RNA与另一种形式的RNAP(携带主要σ因子的全酶)结合。除了在工业和医学上重要的[此处原文缺失相关内容]外,6S RNA在细菌界广泛存在。虽然Ms1 RNA是在[此处原文缺失相关内容]中鉴定出来的,但尚不清楚Ms1 RNA是否也存在于其他[此处原文缺失相关内容]物种中。在这里,我们结合基于二级结构相似性的计算搜索和语言基因共线性方法,在[此处原文缺失相关内容]中鉴定出了Ms1 RNA。在[此处原文缺失相关内容]中,Ms1 RNA与先前注释的功能未知的scr3559 sRNA重叠。我们通过实验证实,Ms1 RNA/scr3559在没有主要σ因子HrdB的情况下与RNAP核心结合。随后,我们将该计算方法应用于其他[此处原文缺失相关内容],并在824个[此处原文缺失相关内容]物种中鉴定出Ms1 RNA候选物,揭示了Ms1 RNA是一类广泛存在的与RNAP结合的sRNA,并证明了我们的多因素计算方法能够在进化距离较远的基因组中鉴定出弱保守的sRNA。