<HashMap><database>biostudies-other</database><scores/><additional><omics_type>Unknown</omics_type><submitter>Dutertre Martin</submitter><species>Homo sapiens</species><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-ECPF-GEOD-53474</full_dataset_link><project>EurocanPlatform</project><abstract>Alternative 3’-terminal exons, which use intronic polyadenylation sites, are generally unconserved and lowly expressed, while the main gene products end in the last exon of genes. In this study, we discover a class of human genes, where the last exon appeared recently during evolution, and the major gene product uses an alternative 3’-terminal exon corresponding to the ancestral last exon of the gene. This novel class of alternative 3’-terminal exons are down-regulated on a large scale by doxorubicin, a cytostatic drug targeting topoisomerase II, and play a role in cell cycle regulation, including centromere-kinetochore assembly. The RNA-binding protein, HuR/ELAVL1 is a major regulator of this specific set of alternative 3’-terminal exons. HuR binding to the alternative 3’-terminal exon in</abstract><repository>biostudies-other</repository><experiment_type>transcription profiling by array</experiment_type><data_source>EurocanPlatform</data_source><pubmed_authors>Combe Emmanuel</pubmed_authors><pubmed_authors>Polay Espinoza Micaela</pubmed_authors><pubmed_authors>Dutertre Martin</pubmed_authors><pubmed_authors>Zahra Chakrama Fatima</pubmed_authors><pubmed_authors>Desmet François-Olivier</pubmed_authors><pubmed_authors>Mortada Hussein</pubmed_authors><pubmed_authors>Gratadou Lise</pubmed_authors><pubmed_authors>Auboeuf Didier</pubmed_authors></additional><is_claimable>false</is_claimable><name>A novel class of alternative 3?-terminal exons is involved in cell-cycle regulation by topoisomerase inhibitors</name><description>Alternative 3’-terminal exons, which use intronic polyadenylation sites, are generally unconserved and lowly expressed, while the main gene products end in the last exon of genes. In this study, we discover a class of human genes, where the last exon appeared recently during evolution, and the major gene product uses an alternative 3’-terminal exon corresponding to the ancestral last exon of the gene. This novel class of alternative 3’-terminal exons are down-regulated on a large scale by doxorubicin, a cytostatic drug targeting topoisomerase II, and play a role in cell cycle regulation, including centromere-kinetochore assembly. The RNA-binding protein, HuR/ELAVL1 is a major regulator of this specific set of alternative 3’-terminal exons. HuR binding to the alternative 3’-terminal exon in</description><dates><release>2016-04-14T14:33:26Z</release><modification>2016-04-14T14:33:26Z</modification><creation>2016-04-14T14:33:26Z</creation></dates><accession>S-ECPF-GEOD-53474</accession><cross_references><GEO>GSE53474</GEO><ArrayExpress>E-GEOD-53474</ArrayExpress><EFO>EFO_0000305</EFO><EFO>EFO_0000322</EFO><ArrayExpress files>E-GEOD-53474</ArrayExpress files></cross_references></HashMap>