<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Bhuiyan SA</submitter><funding>University of British Columbia</funding><pagination>842</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12465193</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>26(1)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>The degree to which alternative RNA splicing influences the function and structure of voltage gated calcium channel (VGCC) splice variants is poorly understood. Here we used long-read RNA-sequencing to catalog rat Cacna1e (Cav2.3) splice variants, and computationally prioritize which are likely to impact channel function.&lt;h4>Result&lt;/h4>We sequenced Cacna1e transcripts from rat thalamus using Oxford Nanopore sequencing yielding the structure of 2,110 Cacna1e splice variants. Of these, up to 154 had the potential encode for a functional channel based on predicted amino acid sequences. Our analysis revealed a total of 31 cassette splicing events (in various combinations) potentially affecting channel function, with three cassette exons appreciably expressed and conserved.&lt;h</pubmed_abstract><journal>BMC genomics</journal><pubmed_title>Cataloging the potential functional diversity of Cacna1e splice variants using long-read sequencing.</pubmed_title><pmcid>PMC12465193</pmcid><funding_grant_id>Michael Smith Laboratories Kickstart</funding_grant_id><pubmed_authors>Pavlidis P</pubmed_authors><pubmed_authors>Snutch TP</pubmed_authors><pubmed_authors>Bhuiyan SA</pubmed_authors><pubmed_authors>Belmadani M</pubmed_authors><pubmed_authors>Tyson JR</pubmed_authors><pubmed_authors>Sicherman J</pubmed_authors></additional><is_claimable>false</is_claimable><name>Cataloging the potential functional diversity of Cacna1e splice variants using long-read sequencing.</name><description>&lt;h4>Background&lt;/h4>The degree to which alternative RNA splicing influences the function and structure of voltage gated calcium channel (VGCC) splice variants is poorly understood. Here we used long-read RNA-sequencing to catalog rat Cacna1e (Cav2.3) splice variants, and computationally prioritize which are likely to impact channel function.&lt;h4>Result&lt;/h4>We sequenced Cacna1e transcripts from rat thalamus using Oxford Nanopore sequencing yielding the structure of 2,110 Cacna1e splice variants. Of these, up to 154 had the potential encode for a functional channel based on predicted amino acid sequences. Our analysis revealed a total of 31 cassette splicing events (in various combinations) potentially affecting channel function, with three cassette exons appreciably expressed and conserved.&lt;h</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Sep</publication><modification>2026-06-03T23:16:36.26Z</modification><creation>2026-05-03T03:10:11.324Z</creation></dates><accession>S-EPMC12465193</accession><cross_references><pubmed>41013183</pubmed><doi>10.1186/s12864-025-11887-1</doi></cross_references></HashMap>