<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>14(9)</volume><submitter>Prezioso C</submitter><pubmed_abstract>Since the non-coding control region (NCCR) and microRNA (miRNA) could represent two different and independent modalities of regulating JC polyomavirus (JCPyV) replication at the transcriptional and post-transcriptional levels, the interplay between JC viral load based on NCCR architecture and miRNA levels, following JCPyV infection with archetypal and rearranged (&lt;i>rr&lt;/i>)-NCCR JCPyV variants, was explored in COS-7 and SVGp12 cells infected by different JCPyV strains. Specifically, the involvement of JCPyV miRNA in regulating viral replication was investigated for the archetypal CY strain-which is the transmissible form-and for the rearranged MAD-1 strain, which is the first isolated variant from patients with progressive multifocal leukoencephalopathy. The JCPyV DNA viral load was low in</pubmed_abstract><journal>Viruses</journal><pagination>2070</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9502812</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>COS-7 and SVGp12 Cellular Models to Study JCPyV Replication and MicroRNA Expression after Infection with Archetypal and Rearranged-NCCR Viral Strains.</pubmed_title><pmcid>PMC9502812</pmcid><pubmed_authors>Passerini S</pubmed_authors><pubmed_authors>Moens U</pubmed_authors><pubmed_authors>Prezioso C</pubmed_authors><pubmed_authors>Palamara AT</pubmed_authors><pubmed_authors>Pietropaolo V</pubmed_authors><pubmed_authors>Limongi D</pubmed_authors></additional><is_claimable>false</is_claimable><name>COS-7 and SVGp12 Cellular Models to Study JCPyV Replication and MicroRNA Expression after Infection with Archetypal and Rearranged-NCCR Viral Strains.</name><description>Since the non-coding control region (NCCR) and microRNA (miRNA) could represent two different and independent modalities of regulating JC polyomavirus (JCPyV) replication at the transcriptional and post-transcriptional levels, the interplay between JC viral load based on NCCR architecture and miRNA levels, following JCPyV infection with archetypal and rearranged (&lt;i>rr&lt;/i>)-NCCR JCPyV variants, was explored in COS-7 and SVGp12 cells infected by different JCPyV strains. Specifically, the involvement of JCPyV miRNA in regulating viral replication was investigated for the archetypal CY strain-which is the transmissible form-and for the rearranged MAD-1 strain, which is the first isolated variant from patients with progressive multifocal leukoencephalopathy. The JCPyV DNA viral load was low in</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Sep</publication><modification>2025-04-21T14:30:42.034Z</modification><creation>2024-11-08T16:59:00.222Z</creation></dates><accession>S-EPMC9502812</accession><cross_references><pubmed>36146876</pubmed><doi>10.3390/v14092070</doi></cross_references></HashMap>