(TA)8 allele in the UGT1A1 gene promoter of a Caucasian with Gilbert's syndrome

Achille Iolascon, Maria Felicia Faienza, Marta Centra, Sonia Storelli, Leopoldo Zelante, Anna Savoia

Research output: Contribution to journalArticle

Abstract

Background and Objective. Gilbert's syndrome, a chronic non-hemolytic unconjugated hyperbilirubinemia, is caused by a reduction in the activity of hepatic bilirubin UDP-glucuronosyltransferase (UGT1A1). This reduction has been shown to be due to a polymorphism in the promoter region of the UGT1A1 gene. The presence of seven thymine adenine (TA) repeats reduces the efficiency of transcription of the UGT1A1 gene. To elucidate the genetic background of a patient affected by Gilbert's syndrome, we collected blood samples from family members for the analysis of the A(TA)(n)TAA motif in the promoter region of the UGT1A1 gene. Design and Methods. Analysis of the A(TA)(n)TAA motif in the promoter region of the UGT1A1 gene was performed by PCR. Estimation of UGT1A1 promoter containing the variable (TA) repeats was performed by using a luciferase reporter system. Results. Three different genotypes were identified due to the presence of (TA)6, (TA)7 and (TA)8 repeats. The production of luciferase decreases in inverse relation to the number of repeats. Interpretation and Conclusions. The (TA)7 polymorphism, associated with Gilbert syndrome, is the only allele found up to now in white populations, while two other variants (TA)5 and (TA)8 have been identified in black populations. We describe here the first case of a subject affected by Gilbert's syndrome who is heterozygous for the (TA)8 allele in the promoter region of the UGT1A1 gene. This polymorphism, as well as the (TA)7 one, is associated with an increased level of bilirubin and a significant reduction of transcription activity of the UGT1A1 gene.

Original languageEnglish
Pages (from-to)106-109
Number of pages4
JournalHaematologica
Volume84
Issue number2
Publication statusPublished - 1999

Fingerprint

Gilbert Disease
Thymine
Adenine
Alleles
Genes
Genetic Promoter Regions
bilirubin glucuronoside glucuronosyltransferase
Luciferases
Hyperbilirubinemia
Bilirubin
Population
Genotype

Keywords

  • Gilbert's syndrome
  • Hyperbilirubinemia
  • Jaundice
  • TA repeat
  • UGT1

ASJC Scopus subject areas

  • Hematology

Cite this

Iolascon, A., Faienza, M. F., Centra, M., Storelli, S., Zelante, L., & Savoia, A. (1999). (TA)8 allele in the UGT1A1 gene promoter of a Caucasian with Gilbert's syndrome. Haematologica, 84(2), 106-109.

(TA)8 allele in the UGT1A1 gene promoter of a Caucasian with Gilbert's syndrome. / Iolascon, Achille; Faienza, Maria Felicia; Centra, Marta; Storelli, Sonia; Zelante, Leopoldo; Savoia, Anna.

In: Haematologica, Vol. 84, No. 2, 1999, p. 106-109.

Research output: Contribution to journalArticle

Iolascon, A, Faienza, MF, Centra, M, Storelli, S, Zelante, L & Savoia, A 1999, '(TA)8 allele in the UGT1A1 gene promoter of a Caucasian with Gilbert's syndrome', Haematologica, vol. 84, no. 2, pp. 106-109.
Iolascon A, Faienza MF, Centra M, Storelli S, Zelante L, Savoia A. (TA)8 allele in the UGT1A1 gene promoter of a Caucasian with Gilbert's syndrome. Haematologica. 1999;84(2):106-109.
Iolascon, Achille ; Faienza, Maria Felicia ; Centra, Marta ; Storelli, Sonia ; Zelante, Leopoldo ; Savoia, Anna. / (TA)8 allele in the UGT1A1 gene promoter of a Caucasian with Gilbert's syndrome. In: Haematologica. 1999 ; Vol. 84, No. 2. pp. 106-109.
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AU - Iolascon, Achille

AU - Faienza, Maria Felicia

AU - Centra, Marta

AU - Storelli, Sonia

AU - Zelante, Leopoldo

AU - Savoia, Anna

PY - 1999

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AB - Background and Objective. Gilbert's syndrome, a chronic non-hemolytic unconjugated hyperbilirubinemia, is caused by a reduction in the activity of hepatic bilirubin UDP-glucuronosyltransferase (UGT1A1). This reduction has been shown to be due to a polymorphism in the promoter region of the UGT1A1 gene. The presence of seven thymine adenine (TA) repeats reduces the efficiency of transcription of the UGT1A1 gene. To elucidate the genetic background of a patient affected by Gilbert's syndrome, we collected blood samples from family members for the analysis of the A(TA)(n)TAA motif in the promoter region of the UGT1A1 gene. Design and Methods. Analysis of the A(TA)(n)TAA motif in the promoter region of the UGT1A1 gene was performed by PCR. Estimation of UGT1A1 promoter containing the variable (TA) repeats was performed by using a luciferase reporter system. Results. Three different genotypes were identified due to the presence of (TA)6, (TA)7 and (TA)8 repeats. The production of luciferase decreases in inverse relation to the number of repeats. Interpretation and Conclusions. The (TA)7 polymorphism, associated with Gilbert syndrome, is the only allele found up to now in white populations, while two other variants (TA)5 and (TA)8 have been identified in black populations. We describe here the first case of a subject affected by Gilbert's syndrome who is heterozygous for the (TA)8 allele in the promoter region of the UGT1A1 gene. This polymorphism, as well as the (TA)7 one, is associated with an increased level of bilirubin and a significant reduction of transcription activity of the UGT1A1 gene.

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