<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Mariano A</submitter><funding>Sapienza University of Rome</funding><pagination>8123</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12427997</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>26(17)</volume><pubmed_abstract>Intron retention (IR) is one of the cellular mechanisms to perform alternative splicing and thus control gene expression in several mammalian cellular pathways. IR in &lt;i>PI-PLC γ1&lt;/i> mRNA was observed in some primary synoviocyte samples from osteoarthritis (OA) patients, likely due to inter-patient variability. The aim of the present manuscript was to explore the &lt;i>PI-PLC γ1&lt;/i> IR molecular mechanism as a consequence of nutraceutical treatment of synoviocytes and the molecular basis of individual response. To evaluate the gene expression modulation of molecules involved in mRNA splicing, an RNA-seq analysis was performed, and the transcription modulation of six differentially expressed genes was validated by RT-PCR. Moreover, through a silencing experiment, the relationship between &lt;i>P</pubmed_abstract><journal>International journal of molecular sciences</journal><pubmed_title>Molecular Basis of Intron Retention in &amp;lt;i&amp;gt;PI-PLC γ1&amp;lt;/i&amp;gt; mRNA from Osteoarthritis Synoviocytes.</pubmed_title><pmcid>PMC12427997</pmcid><funding_grant_id>RP123188E2A80E21; AR2221814F245931</funding_grant_id><pubmed_authors>Mattioli R</pubmed_authors><pubmed_authors>Ammendola S</pubmed_authors><pubmed_authors>Mariano A</pubmed_authors><pubmed_authors>D'Andrea D</pubmed_authors><pubmed_authors>Scotto d'Abusco A</pubmed_authors></additional><is_claimable>false</is_claimable><name>Molecular Basis of Intron Retention in &amp;lt;i&amp;gt;PI-PLC γ1&amp;lt;/i&amp;gt; mRNA from Osteoarthritis Synoviocytes.</name><description>Intron retention (IR) is one of the cellular mechanisms to perform alternative splicing and thus control gene expression in several mammalian cellular pathways. IR in &lt;i>PI-PLC γ1&lt;/i> mRNA was observed in some primary synoviocyte samples from osteoarthritis (OA) patients, likely due to inter-patient variability. The aim of the present manuscript was to explore the &lt;i>PI-PLC γ1&lt;/i> IR molecular mechanism as a consequence of nutraceutical treatment of synoviocytes and the molecular basis of individual response. To evaluate the gene expression modulation of molecules involved in mRNA splicing, an RNA-seq analysis was performed, and the transcription modulation of six differentially expressed genes was validated by RT-PCR. Moreover, through a silencing experiment, the relationship between &lt;i>P</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Aug</publication><modification>2026-04-08T19:51:44.732Z</modification><creation>2026-04-08T14:35:29.421Z</creation></dates><accession>S-EPMC12427997</accession><cross_references><pubmed>40943050</pubmed><doi>10.3390/ijms26178123</doi></cross_references></HashMap>