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http://purl.uniprot.org/citations/27059143http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/27059143http://www.w3.org/2000/01/rdf-schema#comment"Methionine sulfoxide reductase B3 (MsrB3), which is primarily found in the endoplasmic reticulum (ER), is an important protein repair enzyme that stereospecifically reduces methionine-R-sulfoxide residues. We previously found that MsrB3 deficiency arrests the cell cycle at the G1/S stage through up-regulation of p21 and p27. In this study, we report a critical role of MsrB3 in gene expression of heme oxygenase-1 (HO-1), which has an anti-proliferative effect associated with p21 up-regulation. Depletion of MsrB3 elevated HO-1 expression in mammalian cells, whereas MsrB3 overexpression had no effect. MsrB3 deficiency increased cellular reactive oxygen species (ROS), particularly in the mitochondria. ER stress, which is associated with up-regulation of HO-1, was also induced by depletion of MsrB3. Treatment with N-acetylcysteine as an ROS scavenger reduced augmented HO-1 levels in MsrB3-depleted cells. MsrB3 deficiency activated Nrf2 transcription factor by enhancing its expression and nuclear import. The activation of Nrf2 induced by MsrB3 depletion was confirmed by increased expression levels of its other target genes, such as γ-glutamylcysteine ligase. Taken together, these data suggest that MsrB3 attenuates HO-1 induction by inhibiting ROS production, ER stress, and Nrf2 activation."xsd:string
http://purl.uniprot.org/citations/27059143http://purl.org/dc/terms/identifier"doi:10.1016/j.bbrc.2016.04.011"xsd:string
http://purl.uniprot.org/citations/27059143http://purl.uniprot.org/core/author"Kim K.Y."xsd:string
http://purl.uniprot.org/citations/27059143http://purl.uniprot.org/core/author"Kim H.Y."xsd:string
http://purl.uniprot.org/citations/27059143http://purl.uniprot.org/core/author"Kwak G.H."xsd:string
http://purl.uniprot.org/citations/27059143http://purl.uniprot.org/core/date"2016"xsd:gYear
http://purl.uniprot.org/citations/27059143http://purl.uniprot.org/core/name"Biochem Biophys Res Commun"xsd:string
http://purl.uniprot.org/citations/27059143http://purl.uniprot.org/core/pages"1033-1038"xsd:string
http://purl.uniprot.org/citations/27059143http://purl.uniprot.org/core/title"Methionine sulfoxide reductase B3 deficiency stimulates heme oxygenase-1 expression via ROS-dependent and Nrf2 activation pathways."xsd:string
http://purl.uniprot.org/citations/27059143http://purl.uniprot.org/core/volume"473"xsd:string
http://purl.uniprot.org/citations/27059143http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/27059143
http://purl.uniprot.org/citations/27059143http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/27059143
http://purl.uniprot.org/uniprot/#_A0A0R4J139-mappedCitation-27059143http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/27059143
http://purl.uniprot.org/uniprot/#_D3YUC9-mappedCitation-27059143http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/27059143
http://purl.uniprot.org/uniprot/#_Q8BU85-mappedCitation-27059143http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/27059143
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http://purl.uniprot.org/uniprot/#_Q6MZU8-mappedCitation-27059143http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/27059143
http://purl.uniprot.org/uniprot/Q8IXL7http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/27059143
http://purl.uniprot.org/uniprot/Q6MZU8http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/27059143
http://purl.uniprot.org/uniprot/A0A0R4J139http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/27059143
http://purl.uniprot.org/uniprot/Q8BU85http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/27059143
http://purl.uniprot.org/uniprot/D3YUC9http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/27059143