Publication:
Emetine Regulates the Alternative Splicing of Bcl-x through a Protein Phosphatase 1-Dependent Mechanism

dc.contributor.authorKritsanapol Boon-Ungeen_US
dc.contributor.authorQingming Yuen_US
dc.contributor.authorTie Zouen_US
dc.contributor.authorAn Zhouen_US
dc.contributor.authorPiyarat Govitrapongen_US
dc.contributor.authorJianhua Zhouen_US
dc.contributor.otherUniversity of Massachusetts Medical Schoolen_US
dc.contributor.otherMahidol Universityen_US
dc.date.accessioned2018-08-24T01:45:29Z
dc.date.available2018-08-24T01:45:29Z
dc.date.issued2007-12-26en_US
dc.description.abstractExon 2 of the Bcl-x gene undergoes alternative splicing in which the Bcl-xS splice variant promotes apoptosis in contrast to the anti-apoptotic splice variant Bcl-xL. In this study, the regulation of the alternative splicing of pre-mRNA of Bcl-x was examined in response to emetine. Treatment of different types of cancer cells with emetine dihydrochloride downregulated the level of Bcl-xL mRNA with a concomitant increase in the mRNA level of Bcl-xS in a dose- and time-dependent manner. Pretreatment with calyculin A, an inhibitor of protein phosphatase 1 (PP1) and protein phosphatase 2A (PP2A), blocked emetine-induced alternative splicing in contrast to okadaic acid, a specific inhibitor of PP2A in cells, demonstrating a PP1-mediated mechanism. Our finding on the regulation of RNA splicing of members of the Bcl-2 family in response to emetine presents a potential target for cancer treatment. © 2007 Elsevier Ltd. All rights reserved.en_US
dc.identifier.citationChemistry and Biology. Vol.14, No.12 (2007), 1386-1392en_US
dc.identifier.doi10.1016/j.chembiol.2007.11.004en_US
dc.identifier.issn10745521en_US
dc.identifier.other2-s2.0-37149011077en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/24325
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=37149011077&origin=inwarden_US
dc.subjectChemistryen_US
dc.titleEmetine Regulates the Alternative Splicing of Bcl-x through a Protein Phosphatase 1-Dependent Mechanismen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=37149011077&origin=inwarden_US

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