dc.creatorSolari, Claudia María
dc.creatorPetrone Parcero, María Victoria
dc.creatorToro, Ayelen Rayen
dc.creatorVazquez Echegaray, Camila
dc.creatorCosentino, María Soledad
dc.creatorWaisman, Ariel
dc.creatorFrancia, Marcos Gabriel
dc.creatorBarañao, Jose Lino Salvador
dc.creatorMiriuka, Santiago Gabriel
dc.creatorGuberman, Alejandra Sonia
dc.date.accessioned2020-12-04T13:46:21Z
dc.date.accessioned2022-10-15T05:45:07Z
dc.date.available2020-12-04T13:46:21Z
dc.date.available2022-10-15T05:45:07Z
dc.date.created2020-12-04T13:46:21Z
dc.date.issued2019-07
dc.identifierSolari, Claudia María; Petrone Parcero, María Victoria; Toro, Ayelen Rayen; Vazquez Echegaray, Camila; Cosentino, María Soledad; et al.; The pluripotency transcription factor Nanog represses glutathione reductase gene expression in mouse embryonic stem cells; BioMed Central; BMC Research Notes; 12; 1; 7-2019; 1-7
dc.identifier1756-0500
dc.identifierhttp://hdl.handle.net/11336/119834
dc.identifierCONICET Digital
dc.identifierCONICET
dc.identifier.urihttps://repositorioslatinoamericanos.uchile.cl/handle/2250/4351300
dc.description.abstractObjective: Redox homeostasis maintenance is essential to bring about cellular functions. Particularly, embryonic stem cells (ESCs) have high fidelity mechanisms for DNA repair, high activity of different antioxidant enzymes and low levels of oxidative stress. Although the expression and activity of antioxidant enzymes are reduced throughout the differentiation, the knowledge about the transcriptional regulation of genes involved in defense against oxidative stress is yet restricted. Since glutathione is a central component of a complex system involved in preserving cellular redox status, we aimed to study whether the expression of the glutathione reductase (Gsr) gene, which encodes an essential enzyme for cellular redox homeostasis, is modulated by the transcription factors critical for self-renewal and pluripotency of ESCs. Results: We found that Gsr gene is expressed in ESCs during the pluripotent state and it was upregulated when these cells were induced to differentiate, concomitantly with Nanog decreased expression. Moreover, we found an increase in Gsr mRNA levels when Nanog was downregulated by a specific shRNA targeting this transcription factor in ESCs. Our results suggest that Nanog represses Gsr gene expression in ESCs, evidencing a role of this crucial pluripotency transcription factor in preservation of redox homeostasis in stem cells.
dc.languageeng
dc.publisherBioMed Central
dc.relationinfo:eu-repo/semantics/altIdentifier/url/https://bmcresnotes.biomedcentral.com/articles/10.1186/s13104-019-4411-0
dc.relationinfo:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.1186/s13104-019-4411-0
dc.rightshttps://creativecommons.org/licenses/by/2.5/ar/
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectDIFFERENTIATION
dc.subjectEMBRYONIC STEM CELLS
dc.subjectGENE EXPRESSION
dc.subjectGLUTATHIONE REDUCTASE
dc.subjectNANOG
dc.subjectREDOX HOMEOSTASIS
dc.subjectTRANSCRIPTIONAL REGULATION
dc.titleThe pluripotency transcription factor Nanog represses glutathione reductase gene expression in mouse embryonic stem cells
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:ar-repo/semantics/artículo
dc.typeinfo:eu-repo/semantics/publishedVersion


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