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dc.contributor.authorNytofte, N. S.
dc.contributor.authorSerrano García, María Ángeles 
dc.contributor.authorMonte Río, María Jesús 
dc.contributor.authorGonzalez-Sanchez, E.
dc.contributor.authorTumer, Z.
dc.contributor.authorLadefoged, K.
dc.contributor.authorBriz Sánchez, Oscar 
dc.contributor.authorGarcía Marín, José Juan 
dc.date.accessioned2025-01-27T16:08:23Z
dc.date.available2025-01-27T16:08:23Z
dc.date.issued2011
dc.identifier.citationNytofte, N. S., Serrano, M. A., Monte, M. J., Gonzalez-Sanchez, E., Tumer, Z., Ladefoged, K., ... & Marin, J. J. (2011). A homozygous nonsense mutation (c. 214C→ A) in the biliverdin reductase alpha gene (BLVRA) results in accumulation of biliverdin during episodes of cholestasis. Journal of medical genetics, 48(4), 219-225.es_ES
dc.identifier.issn0022-2593
dc.identifier.urihttp://hdl.handle.net/10366/162983
dc.description.abstract[EN] Background: Green jaundice is a rare finding usually associated with end-stage liver disease. Objective: The authors investigated two unrelated Inuit women from different geographical areas in Greenland who had episodes of green jaundice associated with biliary obstruction. Methods and results: The crises were accompanied by increased biochemical markers of cholestasis, together with absent or moderate hyperbilirubinaemia. In contrast, high-performance liquid chromatography tandem mass spectrometry showed hypercholanaemia and high concentrations of biliverdin IXα in serum, urine, bile and milk. Hyperbiliverdinaemia disappeared after surgical correction of the cholestasis. Analysis of the coding sequence of the biliverdin reductase alpha (BVRα) gene (BLVRA) detected three single-nucleotide polymorphisms: c.90G→A, c.214C→A and c.743A→C, which result in p.Ala3Thr, p.Ser44X and p.Gly220Gly, respectively. With the use of TaqMan probes, homozygosity for c.214C→A was found in both patients. Both parents of one of these patients were heterozygous for the inactivating mutation. Her brother was homozygous for normal alleles. Although her sister was also homozygous for the c.214C→A mutation, she had never had hyperbiliverdinaemia or cholestasis. With the use of human liver RNA, the BVRa coding sequence was cloned, and the variant containing c.214C→A was generated by site-directed mutagenesis. Both proteins were expressed in human hepatoma liver cells and Xenopus laevis oocytes. Immunoblotting, immunofluorescence and functional assays of BVRa activity revealed that the mutated sequence generates a truncated protein with no catalytic activity. Conclusion: This is the first report of a homozygous BLVRA inactivating mutation indicating that the complete absence of BVRα activity is a non-lethal condition, the most evident phenotypic characteristic of which is the appearance of green jaundice accompanying cholestasis episodes.es_ES
dc.format.mimetypeapplication/pdf
dc.language.isoenges_ES
dc.publisherBMJ Groupes_ES
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subjectBiliverdin Reductasees_ES
dc.subjectCholestasises_ES
dc.subject.meshDNA Mutational Analysis *
dc.subject.meshCholestasis *
dc.titleA homozygous nonsense mutation (c.214C->A) in the biliverdin reductase alpha gene (BLVRA) results in accumulation of biliverdin during episodes of cholestasises_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.relation.publishversionhttps://doi.org/10.1136/jmg.2009.074567es_ES
dc.subject.unesco3209 Farmacologíaes_ES
dc.identifier.doi10.1136/jmg.2009.074567
dc.rights.accessRightsinfo:eu-repo/semantics/closedAccesses_ES
dc.identifier.pmid21278388
dc.identifier.essn1468-6244
dc.journal.titleJournal of Medical Geneticses_ES
dc.volume.number48es_ES
dc.issue.number4es_ES
dc.page.initial219es_ES
dc.page.final225es_ES
dc.type.hasVersioninfo:eu-repo/semantics/publishedVersiones_ES
dc.subject.decsanálisis de mutaciones del ADN *
dc.subject.decscolestasis *


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