<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Rios-Delgado G</submitter><funding>National Institute of Allergy and Infectious Diseases</funding><funding>Agence Nationale de la Recherche</funding><funding>U.S. Department of Agriculture</funding><funding>NIAID NIH HHS</funding><funding>National Science Foundation</funding><pagination>e0141525</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12607789</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>16(11)</volume><pubmed_abstract>Bacterial regulatory RNAs (sRNAs) are commonly short non-coding RNAs that function as pleiotropic regulators by post-transcriptionally impacting mRNA stability and/or translation. They play significant roles in bacterial physiology and are typically expressed in response to specific environmental stimuli such as nutrient limitation. The bacterial pathogen &lt;i>Staphylococcus aureus&lt;/i> faces decreased access to essential metal ions, including iron, in the mammalian host via a process called nutritional immunity. In response to host-mediated iron limitation, &lt;i>S. aureus&lt;/i> expresses the sRNA IsrR, which coordinates an iron-sparing response by downregulating the expression of mRNAs coding for iron-requiring proteins or processes. Herein, we utilized MS2-Affinity Purification coupled with RNA</pubmed_abstract><journal>mBio</journal><pubmed_title>The iron-regulated small regulatory RNA IsrR modulates expression of genes utilized for dioxygen metabolism and heme synthesis in &amp;lt;i&amp;gt;Staphylococcus aureus&amp;lt;/i&amp;gt;.</pubmed_title><pmcid>PMC12607789</pmcid><funding_grant_id>R01 AI139100</funding_grant_id><funding_grant_id>R01 AI155611</funding_grant_id><funding_grant_id>ANR-20-CE12-0021</funding_grant_id><funding_grant_id>ANR-10-IDEX-0002</funding_grant_id><funding_grant_id>AI155611</funding_grant_id><funding_grant_id>1750624</funding_grant_id><funding_grant_id>ANR-17-EURE-0023</funding_grant_id><funding_grant_id>ANR-20-SFRI-0012</funding_grant_id><funding_grant_id>NE-2248</funding_grant_id><pubmed_authors>Lalaouna D</pubmed_authors><pubmed_authors>Kehl-Fie T</pubmed_authors><pubmed_authors>Rios-Delgado G</pubmed_authors><pubmed_authors>Boyd JM</pubmed_authors><pubmed_authors>McFarlane R</pubmed_authors><pubmed_authors>Kim J</pubmed_authors><pubmed_authors>Zheng V</pubmed_authors><pubmed_authors>Parker D</pubmed_authors></additional><is_claimable>false</is_claimable><name>The iron-regulated small regulatory RNA IsrR modulates expression of genes utilized for dioxygen metabolism and heme synthesis in &amp;lt;i&amp;gt;Staphylococcus aureus&amp;lt;/i&amp;gt;.</name><description>Bacterial regulatory RNAs (sRNAs) are commonly short non-coding RNAs that function as pleiotropic regulators by post-transcriptionally impacting mRNA stability and/or translation. They play significant roles in bacterial physiology and are typically expressed in response to specific environmental stimuli such as nutrient limitation. The bacterial pathogen &lt;i>Staphylococcus aureus&lt;/i> faces decreased access to essential metal ions, including iron, in the mammalian host via a process called nutritional immunity. In response to host-mediated iron limitation, &lt;i>S. aureus&lt;/i> expresses the sRNA IsrR, which coordinates an iron-sparing response by downregulating the expression of mRNAs coding for iron-requiring proteins or processes. Herein, we utilized MS2-Affinity Purification coupled with RNA</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Nov</publication><modification>2026-06-05T13:52:07.655Z</modification><creation>2026-05-17T03:13:02.351Z</creation></dates><accession>S-EPMC12607789</accession><cross_references><pubmed>41042061</pubmed><doi>10.1128/mbio.01415-25</doi></cross_references></HashMap>