{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"omics_type":["Unknown"],"volume":["12"],"submitter":["Zhou J"],"pubmed_abstract":["<h4>Aim</h4>Our previous proteomic analysis showed that small RNA SprC (one of the small pathogenicity island RNAs) of <i>Staphylococcus aureus</i> possesses the ability to regulate the expression of multiple bacterial proteins. In this study, our objective was to further provide insights into the regulatory role of SprC in gene transcription and metabolism of <i>S. aureus</i>.<h4>Methods</h4>Gene expression profiles were obtained from <i>S. aureus</i> N315 wild-type and its <i>sprC</i> deletion mutant strains by RNA-sequencing (RNA-seq), and differentially expressed genes (DEGs) were screened by R language with a |log2(fold change)| ≥1 and a false discovery rate (FDR) ≤ 0.05. Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway analysis were carried out to underst"],"journal":["Frontiers in cellular and infection microbiology"],"pagination":["746746"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC8905650"],"repository":["biostudies-literature"],"pubmed_title":["Insights Into the Impact of Small RNA SprC on the Metabolism and Virulence of <i>Staphylococcus aureus</i>."],"pmcid":["PMC8905650"],"pubmed_authors":["Yang H","He C","Shu W","Cui Z","Liu Q","Zhou J","Zhao H"],"additional_accession":[]},"is_claimable":false,"name":"Insights Into the Impact of Small RNA SprC on the Metabolism and Virulence of <i>Staphylococcus aureus</i>.","description":"<h4>Aim</h4>Our previous proteomic analysis showed that small RNA SprC (one of the small pathogenicity island RNAs) of <i>Staphylococcus aureus</i> possesses the ability to regulate the expression of multiple bacterial proteins. In this study, our objective was to further provide insights into the regulatory role of SprC in gene transcription and metabolism of <i>S. aureus</i>.<h4>Methods</h4>Gene expression profiles were obtained from <i>S. aureus</i> N315 wild-type and its <i>sprC</i> deletion mutant strains by RNA-sequencing (RNA-seq), and differentially expressed genes (DEGs) were screened by R language with a |log2(fold change)| ≥1 and a false discovery rate (FDR) ≤ 0.05. Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway analysis were carried out to underst","dates":{"release":"2022-01-01T00:00:00Z","publication":"2022","modification":"2026-05-30T14:41:33.575Z","creation":"2024-11-05T18:34:40.44Z"},"accession":"S-EPMC8905650","cross_references":{"pubmed":["35281456"],"doi":["10.3389/fcimb.2022.746746"]}}