Publication:
PGC-1α regulates translocated in liposarcoma activity: role in oxidative stress gene expression.

dc.contributor.authorSánchez-Ramos, Cristina
dc.contributor.authorTierrez, Alberto
dc.contributor.authorFabregat-Andrés, Oscar
dc.contributor.authorWild, Brigitte
dc.contributor.authorSanchez-Cabo, Fatima
dc.contributor.authorArduini, Alessandro
dc.contributor.authorDopazo, Ana
dc.contributor.authorMonsalve, María
dc.date.accessioned2024-01-31T12:00:28Z
dc.date.available2024-01-31T12:00:28Z
dc.date.issued2011-07-15
dc.description.abstractUNLABELLED Translocated in liposarcoma (TLS) is a poorly characterized multifunctional protein involved in the genotoxic response. TLS regulates gene expression at several steps, including splicing and mRNA transport, possibly connecting transcriptional and posttranscriptional events. AIMS In this study we aimed to idenfity molecular targets and regulatory partners of TLS. RESULTS AND INNOVATION Here we report that TLS transcriptionally regulates the expression of oxidative stress protection genes. This regulation requires interaction with the transcriptional coactivator peroxisome proliferator activated receptor γ-coactivator 1α (PGC-1α), a master regulator of mitochondrial function that coordinately induces the expression of genes involved in detoxification of mitochondrial reactive oxygen species (ROS). Microarray gene expression analysis showed that TLS transcriptional activity is impaired in the absence of PGC-1α, and is thus largely dependent on PGC-1α. CONCLUSION These results suggest the existence of a regulatory circuit linking the control of ROS detoxification to the coordinated cross-talk between oxidative metabolism and the cellular response to genomic DNA damage.es_ES
dc.description.peerreviewedes_ES
dc.format.number2es_ES
dc.format.page325es_ES
dc.format.volume15es_ES
dc.identifier.citationAntioxid Redox Signal. 2011 Jul 15;15(2):325-37.es_ES
dc.identifier.doi10.1089/ars.2010.3643es_ES
dc.identifier.e-issn1557-7716es_ES
dc.identifier.journalAntioxidants & redox signalinges_ES
dc.identifier.pubmedID21338289es_ES
dc.identifier.urihttp://hdl.handle.net/20.500.12105/17389
dc.language.isoenges_ES
dc.publisherMary Ann Liebertes_ES
dc.relation.publisherversion10.1089/ars.2010.3643es_ES
dc.repisalud.institucionCNICes_ES
dc.rights.accessRightsopen accesses_ES
dc.rights.licenseAttribution-NonCommercial-NoDerivatives 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subject.meshAnimalses_ES
dc.subject.meshBase Sequencees_ES
dc.subject.meshCells, Culturedes_ES
dc.subject.meshDNA Primerses_ES
dc.subject.meshEnergy Metabolismes_ES
dc.subject.meshGene Expression Regulationes_ES
dc.subject.meshMicees_ES
dc.subject.meshOxidative Stresses_ES
dc.subject.meshPeroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alphaes_ES
dc.subject.meshRNA-Binding Protein FUSes_ES
dc.subject.meshTrans-Activatorses_ES
dc.subject.meshTranscription Factorses_ES
dc.subject.meshTwo-Hybrid System Techniqueses_ES
dc.titlePGC-1α regulates translocated in liposarcoma activity: role in oxidative stress gene expression.es_ES
dc.typejournal articlees_ES
dc.type.hasVersionVoRes_ES
dspace.entity.typePublication
relation.isAuthorOfPublicationecd7f1e7-2399-4c06-bbc6-d1a2e86c0fbe
relation.isAuthorOfPublication90c95c5b-73c0-44ee-8f23-a0d92a30c789
relation.isAuthorOfPublication.latestForDiscoveryecd7f1e7-2399-4c06-bbc6-d1a2e86c0fbe

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