<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Musiyenko A</submitter><funding>NIAID NIH HHS</funding><pagination>745-52</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC3263383</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>85(7)</volume><pubmed_abstract>Stable RNA interference (RNAi) is commonly achieved by recombinant expression of short hairpin RNA (shRNA). To generate virus-resistant cell lines, we cloned a shRNA cassette against the phosphoprotein gene of respiratory syncytial virus (RSV) into a polIII-driven plasmid vector. Analysis of individual stable transfectants showed a spectrum of RSV resistance correlating with the levels of shRNA expressed from different chromosomal locations. Interestingly, resistance in a minority of clones was due to mono-allelic disruption of the cellular gene for vasodilator-stimulated phosphoprotein (VASP). Thus, pure clones of chromosomally integrated DNA-directed RNAi can exhibit gene disruption phenotypes resembling but unrelated to RNAi.</pubmed_abstract><journal>Journal of molecular medicine (Berlin, Germany)</journal><pubmed_title>RNAi-dependent and -independent antiviral phenotypes of chromosomally integrated shRNA clones: role of VASP in respiratory syncytial virus growth.</pubmed_title><pmcid>PMC3263383</pmcid><funding_grant_id>R01 AI059267</funding_grant_id><funding_grant_id>AI059267</funding_grant_id><funding_grant_id>R01 AI059267-03</funding_grant_id><funding_grant_id>R01 AI059267-04</funding_grant_id><funding_grant_id>R01 AI059267-05</funding_grant_id><funding_grant_id>R01 AI059267-06</funding_grant_id><pubmed_authors>Barik S</pubmed_authors><pubmed_authors>Musiyenko A</pubmed_authors><pubmed_authors>Bitko V</pubmed_authors></additional><is_claimable>false</is_claimable><name>RNAi-dependent and -independent antiviral phenotypes of chromosomally integrated shRNA clones: role of VASP in respiratory syncytial virus growth.</name><description>Stable RNA interference (RNAi) is commonly achieved by recombinant expression of short hairpin RNA (shRNA). To generate virus-resistant cell lines, we cloned a shRNA cassette against the phosphoprotein gene of respiratory syncytial virus (RSV) into a polIII-driven plasmid vector. Analysis of individual stable transfectants showed a spectrum of RSV resistance correlating with the levels of shRNA expressed from different chromosomal locations. Interestingly, resistance in a minority of clones was due to mono-allelic disruption of the cellular gene for vasodilator-stimulated phosphoprotein (VASP). Thus, pure clones of chromosomally integrated DNA-directed RNAi can exhibit gene disruption phenotypes resembling but unrelated to RNAi.</description><dates><release>2007-01-01T00:00:00Z</release><publication>2007 Jul</publication><modification>2025-04-29T09:47:58.169Z</modification><creation>2019-06-05T17:00:33Z</creation></dates><accession>S-EPMC3263383</accession><cross_references><pubmed>17351763</pubmed><doi>10.1007/s00109-007-0179-0</doi></cross_references></HashMap>