<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>23(1)</volume><submitter>Iida K</submitter><pubmed_abstract>&lt;h4>Background&lt;/h4>The SARS-CoV-2 pandemic provided important insights into the relationship between infectious diseases and the human genome. A genomic region encoding the 2'-5'-oligoadenylate synthetase (OAS) family proteins that sense viral genomic RNAs and trigger an antiviral response contains single nucleotide polymorphisms (SNPs) associated with SARS-CoV-2 infection susceptibility. A high-risk SNP identified at the splice acceptor site of OAS1 exon 6-a terminal exon-alters the proportion of various splicing isoforms of OAS1 and its activity. However, the actual causality of this SNP or splicing to infection susceptibility remains unknown.&lt;h4>Results&lt;/h4>In this study, it was found that serine-arginine-rich splicing factor 6 (SRSF6) binds to the splice donor site of the human OAS1 ex</pubmed_abstract><journal>BMC biology</journal><pagination>60</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11874701</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Switching of OAS1 splicing isoforms overcomes SNP-derived vulnerability to SARS-CoV-2 infection.</pubmed_title><pmcid>PMC11874701</pmcid><pubmed_authors>Iida K</pubmed_authors><pubmed_authors>Kurosawa R</pubmed_authors><pubmed_authors>Denawa M</pubmed_authors><pubmed_authors>Noda T</pubmed_authors><pubmed_authors>Ajiro M</pubmed_authors><pubmed_authors>Hagiwara M</pubmed_authors><pubmed_authors>Nakano-Kobayashi A</pubmed_authors><pubmed_authors>Takenaga T</pubmed_authors><pubmed_authors>Muramoto Y</pubmed_authors></additional><is_claimable>false</is_claimable><name>Switching of OAS1 splicing isoforms overcomes SNP-derived vulnerability to SARS-CoV-2 infection.</name><description>&lt;h4>Background&lt;/h4>The SARS-CoV-2 pandemic provided important insights into the relationship between infectious diseases and the human genome. A genomic region encoding the 2'-5'-oligoadenylate synthetase (OAS) family proteins that sense viral genomic RNAs and trigger an antiviral response contains single nucleotide polymorphisms (SNPs) associated with SARS-CoV-2 infection susceptibility. A high-risk SNP identified at the splice acceptor site of OAS1 exon 6-a terminal exon-alters the proportion of various splicing isoforms of OAS1 and its activity. However, the actual causality of this SNP or splicing to infection susceptibility remains unknown.&lt;h4>Results&lt;/h4>In this study, it was found that serine-arginine-rich splicing factor 6 (SRSF6) binds to the splice donor site of the human OAS1 ex</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Mar</publication><modification>2026-06-01T23:10:25.393Z</modification><creation>2025-04-04T02:11:18.956Z</creation></dates><accession>S-EPMC11874701</accession><cross_references><pubmed>40025489</pubmed><doi>10.1186/s12915-025-02173-3</doi></cross_references></HashMap>