<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>38(10)</volume><submitter>Lee KM</submitter><pubmed_abstract>TRAP150 has been identified as a subunit of the transcription regulatory complex TRAP/Mediator, and also a component of the spliceosome. The exact function of TRAP150, however, remains unclear. We recently identified TRAP150 by its association with the mRNA export factor TAP. TRAP150 contains an arginine/serine-rich domain and has sequence similarity with the cell death-promoting transcriptional repressor BCLAF1. We found that TRAP150 co-localizes with splicing factors in nuclear speckles, and is required for pre-mRNA splicing and activates splicing in vivo. TRAP150 remains associated with the spliced mRNA after splicing, and accordingly, it interacts with the integral exon junction complex. Unexpectedly, when tethered to a precursor mRNA, TRAP150 can trigger mRNA degradation in the nucleus. However, unlike nonsense-mediated decay, TRAP150-mediated mRNA decay is irrespective of the presence of upstream stop codons and occurs in the nucleus. Moreover, TRAP150 activates pre-mRNA splicing and induces mRNA degradation by its separable functional domains. Therefore, TRAP150 represents a multi-functional protein involved in nuclear mRNA metabolism.</pubmed_abstract><journal>Nucleic acids research</journal><pagination>3340-50</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC2879504</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>TRAP150 activates pre-mRNA splicing and promotes nuclear mRNA degradation.</pubmed_title><pmcid>PMC2879504</pmcid><pubmed_authors>Tarn WY</pubmed_authors><pubmed_authors>Hsu IaW</pubmed_authors><pubmed_authors>Lee KM</pubmed_authors></additional><is_claimable>false</is_claimable><name>TRAP150 activates pre-mRNA splicing and promotes nuclear mRNA degradation.</name><description>TRAP150 has been identified as a subunit of the transcription regulatory complex TRAP/Mediator, and also a component of the spliceosome. The exact function of TRAP150, however, remains unclear. We recently identified TRAP150 by its association with the mRNA export factor TAP. TRAP150 contains an arginine/serine-rich domain and has sequence similarity with the cell death-promoting transcriptional repressor BCLAF1. We found that TRAP150 co-localizes with splicing factors in nuclear speckles, and is required for pre-mRNA splicing and activates splicing in vivo. TRAP150 remains associated with the spliced mRNA after splicing, and accordingly, it interacts with the integral exon junction complex. Unexpectedly, when tethered to a precursor mRNA, TRAP150 can trigger mRNA degradation in the nucleus. However, unlike nonsense-mediated decay, TRAP150-mediated mRNA decay is irrespective of the presence of upstream stop codons and occurs in the nucleus. Moreover, TRAP150 activates pre-mRNA splicing and induces mRNA degradation by its separable functional domains. Therefore, TRAP150 represents a multi-functional protein involved in nuclear mRNA metabolism.</description><dates><release>2010-01-01T00:00:00Z</release><publication>2010 Jun</publication><modification>2025-04-22T06:42:02.764Z</modification><creation>2019-03-27T00:31:14Z</creation></dates><accession>S-EPMC2879504</accession><cross_references><pubmed>20123736</pubmed><doi>10.1093/nar/gkq017</doi></cross_references></HashMap>