Martins Diogo, Salgueiro Bruno, Sobral Daniel, Gragera Marcos, Hensel Zach, Henriques Adriano O, Romão Célia V, Serrano Mónica
Instituto de Tecnologia Química e Biológica António Xavier, Universidade Nova de Lisboa, Avenida da República EAN, 2780-157 Oeiras, Portugal.
Genomics and Bioinformatics Unit, Department of Infectious Diseases, National Institute of Health Doutor Ricardo Jorge (INSA), Av. Padre Cruz, 1649-016 Lisboa, Portugal.
Nucleic Acids Res. 2025 Jul 8;53(13). doi: 10.1093/nar/gkaf644.
Clostridioides difficile CD25890 is a YicC-like endoribonuclease involved in regulating sporulation initiation, a process critical for the host-host transmission of this anaerobic pathogen. Using comparative transcriptomics we identified a small RNA, SQ528, that accumulates at higher levels in a CD25890 deletion mutant and we show that purified CD25890 cleaves SQ528 in a metal-dependent manner. Moreover, the overexpression of SQ528 increases sporulation under certain nutritional conditions phenocopying a CD25890 deletion mutant. CD25890 is an hexamer in solution and in vivo. An N-terminal domain, which self-interacts as assessed by size exclusion chromatography and a two hybrid assay, is essential for oligomerization of CD25890. A C-terminal domain harbours residues H230, E254, and E258, conserved among orthologues, important for catalysis. AlphaFold2 modelling and cryo-EM suggest an elongated barrel-like structure with an internal cavity lined with basic residues that may aid in RNA binding. We show that CD25890 forms a complex with polynucleotide phosphorylase which combines the endoribonuclease activity of the first with the exonucleolytic activity of the latter and leads to the complete degradation of SQ528. This study identifies a native substrate for the YicC-family of ribonucleases and advances our understanding of the role of CD25890 in sporulation initiation in C. difficile.
艰难梭菌CD25890是一种类似于YicC的内切核糖核酸酶,参与调控芽孢形成起始,这一过程对这种厌氧病原体在宿主间传播至关重要。通过比较转录组学,我们鉴定出一种小RNA,即SQ528,它在CD25890缺失突变体中积累水平更高,并且我们发现纯化的CD25890以金属依赖的方式切割SQ528。此外,在某些营养条件下,SQ528的过表达会增加芽孢形成,其表型类似于CD25890缺失突变体。CD25890在溶液和体内均为六聚体。通过尺寸排阻色谱和双杂交试验评估,一个自我相互作用的N端结构域对CD25890的寡聚化至关重要。一个C端结构域含有在直系同源物中保守的H230、E254和E258残基,对催化作用很重要。AlphaFold2建模和冷冻电镜显示其为一种细长的桶状结构,内部腔室衬有碱性残基,可能有助于RNA结合。我们发现CD25890与多核苷酸磷酸化酶形成复合物,该复合物将前者的内切核糖核酸酶活性与后者的外切核酸酶活性结合起来,导致SQ528完全降解。这项研究鉴定出核糖核酸酶YicC家族的一种天然底物,并加深了我们对CD25890在艰难梭菌芽孢形成起始中作用的理解。