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原噬菌体编码的小蛋白YqaH可抵消复制起始蛋白DnaA在……中的活性。

Prophage-encoded small protein YqaH counteracts the activities of the replication initiator DnaA in .

作者信息

Ventroux Magali, Noirot-Gros Marie-Francoise

机构信息

Université Paris-Saclay, INRAE, AgroParisTech, Micalis Institute, 78350, Jouy-en-Josas, France.

出版信息

Microbiology (Reading). 2022 Nov;168(11). doi: 10.1099/mic.0.001268.

DOI:10.1099/mic.0.001268
PMID:36748575
Abstract

Bacterial genomes harbour cryptic prophages that are mostly transcriptionally silent with many unannotated genes. Still, cryptic prophages may contribute to their host fitness and phenotypes. In the operon belongs to the prophage element , and is tightly repressed by the Xre-like repressor SknR. This operon contains several small ORFs (smORFs) potentially encoding small-sized proteins. The smORF-encoded peptide YqaH was previously reported to bind to the replication initiator DnaA. Here, using a yeast two-hybrid assay, we found that YqaH binds to the DNA binding domain IV of DnaA and interacts with Spo0A, a master regulator of sporulation. We isolated single amino acid substitutions in YqaH that abolished the interaction with DnaA but not with Spo0A. Then, using a plasmid-based inducible system to overexpress WT and mutant derivatives, we studied in the phenotypes associated with the specific loss-of-interaction with DnaA (DnaA_LOI). We found that expression of carrying DnaA_LOI mutations abolished the deleterious effects of WT expression on chromosome segregation, replication initiation and DnaA-regulated transcription. When YqaH was induced after vegetative growth, DnaA_LOI mutations abolished the drastic effects of YqaH WT on sporulation and biofilm formation. Thus, YqaH inhibits replication, sporulation and biofilm formation mainly by antagonizing DnaA in a manner that is independent of the cell cycle checkpoint Sda.

摘要

细菌基因组中含有隐秘原噬菌体,这些原噬菌体大多转录沉默,有许多未注释的基因。尽管如此,隐秘原噬菌体可能会影响其宿主的适应性和表型。在 操纵子属于原噬菌体元件,受到Xre样阻遏物SknR的严格抑制。该操纵子包含几个可能编码小蛋白的小开放阅读框(smORF)。先前报道smORF编码的肽YqaH与复制起始蛋白DnaA结合。在这里,我们使用酵母双杂交试验发现,YqaH与DnaA的DNA结合结构域IV结合,并与芽孢形成的主要调节因子Spo0A相互作用。我们分离出YqaH中的单氨基酸取代,这些取代消除了与DnaA的相互作用,但没有消除与Spo0A的相互作用。然后,使用基于质粒的诱导系统过表达野生型和突变衍生物,我们在 中研究了与DnaA特异性相互作用丧失(DnaA_LOI)相关的表型。我们发现携带DnaA_LOI突变的 的表达消除了野生型表达对染色体分离、复制起始和DnaA调节转录的有害影响。当在营养生长后诱导YqaH时,DnaA_LOI突变消除了YqaH野生型对芽孢形成和生物膜形成的剧烈影响。因此,YqaH主要通过以独立于细胞周期检查点Sda的方式拮抗DnaA来抑制复制、芽孢形成和生物膜形成。

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