<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Qu W</submitter><funding>NIEHS NIH HHS</funding><funding>National Institutes of Health</funding><funding>NIH HHS</funding><pagination>38</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC5387049</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>8</volume><pubmed_abstract>Deep sequencing of cDNAs made from spliced mRNAs indicates that most coding genes in many animals and plants have pre-mRNA transcripts that are alternatively spliced. In pre-mRNAs, in addition to invariant exons that are present in almost all mature mRNA products, there are at least 6 additional types of exons, such as exons from alternative promoters or with alternative polyA sites, mutually exclusive exons, skipped exons, or exons with alternative 5' or 3' splice sites. Our bioinformatics-based hypothesis is that, in analogy to the genetic code, there is an "alternative-splicing code" in introns and flanking exon sequences, analogous to the genetic code, that directs alternative splicing of many of the 36 types of introns. In humans, we identified 42 different consensus sequences that ar</pubmed_abstract><journal>Frontiers in genetics</journal><pubmed_title>A Bioinformatics-Based Alternative mRNA Splicing Code that May Explain Some Disease Mutations Is Conserved in Animals.</pubmed_title><pmcid>PMC5387049</pmcid><funding_grant_id>UH3 OD023285</funding_grant_id><funding_grant_id>S10 OD025170</funding_grant_id><funding_grant_id>P30 ES020957</funding_grant_id><funding_grant_id>ES021983</funding_grant_id><funding_grant_id>R21 ES021983</funding_grant_id><funding_grant_id>UG3 OD023285</funding_grant_id><funding_grant_id>R01 ES012933</funding_grant_id><funding_grant_id>ES020957</funding_grant_id><funding_grant_id>ES012933</funding_grant_id><pubmed_authors>Ruden DM</pubmed_authors><pubmed_authors>Cingolani P</pubmed_authors><pubmed_authors>Zeeberg BR</pubmed_authors><pubmed_authors>Qu W</pubmed_authors></additional><is_claimable>false</is_claimable><name>A Bioinformatics-Based Alternative mRNA Splicing Code that May Explain Some Disease Mutations Is Conserved in Animals.</name><description>Deep sequencing of cDNAs made from spliced mRNAs indicates that most coding genes in many animals and plants have pre-mRNA transcripts that are alternatively spliced. In pre-mRNAs, in addition to invariant exons that are present in almost all mature mRNA products, there are at least 6 additional types of exons, such as exons from alternative promoters or with alternative polyA sites, mutually exclusive exons, skipped exons, or exons with alternative 5' or 3' splice sites. Our bioinformatics-based hypothesis is that, in analogy to the genetic code, there is an "alternative-splicing code" in introns and flanking exon sequences, analogous to the genetic code, that directs alternative splicing of many of the 36 types of introns. In humans, we identified 42 different consensus sequences that ar</description><dates><release>2017-01-01T00:00:00Z</release><publication>2017</publication><modification>2025-04-05T12:13:05.095Z</modification><creation>2019-03-27T02:40:59Z</creation></dates><accession>S-EPMC5387049</accession><cross_references><pubmed>28443131</pubmed><doi>10.3389/fgene.2017.00038</doi></cross_references></HashMap>