Journal of hepatology · 2015
Disruption of HNF1α binding site causes inherited severe unconjugated hyperbilirubinemia.
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van Dijk Remco, Mayayo-Peralta Isabel, Aronson Sem J, Kattentidt-Mouravieva Anja A, van der Mark Vincent A, de Knegt Rob, Oruc Nevin, Beuers Ulrich, Bosma Piter J
Аннотация
Crigler-Najjar syndrome presents as severe unconjugated hyperbilirubinemia and is characteristically caused by a mutation in the UGT1A1 gene, encoding the enzyme responsible for bilirubin glucuronidation. Here we present a patient with Crigler-Najjar syndrome with a completely normal UGT1A1 coding region. Instead, a homozygous 3 nucleotide insertion in the UGT1A1 promoter was identified that interrupts the HNF1α binding site. This mutation results in almost complete abolishment of UGT1A1 promoter activity and prevents the induction of UGT1A1 expression by the liver nuclear receptors CAR and PXR, explaining the lack of a phenobarbital response in this patient. Although animal studies have revealed the importance of HNF1α for normal liver function, this case provides the first clinical proof that mutations in its binding site indeed result in severe liver pathology stressing the importance of promoter sequence analysis.
Предметные рубрики MeSH
AdultBase SequenceBinding SitesConstitutive Androstane ReceptorCrigler-Najjar SyndromeFemaleGlucuronosyltransferaseHepatocyte Nuclear Factor 1-alphaHomozygoteHumansLiverMolecular Sequence DataMutagenesis, InsertionalPromoter Regions, GeneticReceptors, Cytoplasmic and NuclearSequence Analysis, DNATranscription, GeneticUGT1A1 Enzyme