<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Brunkard JO</submitter><funding>Agricultural Research Service</funding><funding>National Institutes of Health</funding><funding>NIH HHS</funding><pagination>1333</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6143672</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>9</volume><pubmed_abstract>The cytosolic RNA exosome, a 3'→5' exoribonuclease complex, contributes to mRNA degradation in eukaryotes, limiting the accumulation of poorly-translated, improperly translated, or aberrant mRNA species. Disruption of cytosolic RNA exosome activity allows aberrant RNA species to accumulate, which can then be detected by host antiviral immune systems as a signature of pathogen infection, activating antiviral defenses. SKI7 is a critical component of the cytosolic RNA exosome in yeast, bridging the catalytic exoribonuclease core with the SKI2/SKI3/SKI8 adaptor complex that guides aberrant RNA substrates into the exosome. The ortholog of &lt;i>SKI7&lt;/i> was only recently identified in humans as an alternative splice form of the &lt;i>HBS1&lt;/i> gene, which encodes a decoding factor translational GTPas</pubmed_abstract><journal>Frontiers in plant science</journal><pubmed_title>A Two-Headed Monster to Avert Disaster: HBS1/SKI7 Is Alternatively Spliced to Build Eukaryotic RNA Surveillance Complexes.</pubmed_title><pmcid>PMC6143672</pmcid><funding_grant_id>5-DP5-OD023072</funding_grant_id><funding_grant_id>DP5 OD023072</funding_grant_id><funding_grant_id>2030-22000-009-00D</funding_grant_id><pubmed_authors>Brunkard JO</pubmed_authors><pubmed_authors>Baker B</pubmed_authors></additional><is_claimable>false</is_claimable><name>A Two-Headed Monster to Avert Disaster: HBS1/SKI7 Is Alternatively Spliced to Build Eukaryotic RNA Surveillance Complexes.</name><description>The cytosolic RNA exosome, a 3'→5' exoribonuclease complex, contributes to mRNA degradation in eukaryotes, limiting the accumulation of poorly-translated, improperly translated, or aberrant mRNA species. Disruption of cytosolic RNA exosome activity allows aberrant RNA species to accumulate, which can then be detected by host antiviral immune systems as a signature of pathogen infection, activating antiviral defenses. SKI7 is a critical component of the cytosolic RNA exosome in yeast, bridging the catalytic exoribonuclease core with the SKI2/SKI3/SKI8 adaptor complex that guides aberrant RNA substrates into the exosome. The ortholog of &lt;i>SKI7&lt;/i> was only recently identified in humans as an alternative splice form of the &lt;i>HBS1&lt;/i> gene, which encodes a decoding factor translational GTPas</description><dates><release>2018-01-01T00:00:00Z</release><publication>2018</publication><modification>2026-04-07T19:53:28.033Z</modification><creation>2026-04-07T17:20:46.552Z</creation></dates><accession>S-EPMC6143672</accession><cross_references><pubmed>30258456</pubmed><doi>10.3389/fpls.2018.01333</doi></cross_references></HashMap>