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Structural and Functional Insights on an Uncharacterized Aγ-Globin-Gene Polymorphism Present in Four β-Thalassemia Families with High Fetal Hemoglobin Levels.
- Source :
- Molecular Diagnosis & Therapy; Apr2016, Vol. 20 Issue 2, p161-173, 13p
- Publication Year :
- 2016
-
Abstract
- Introduction: Several DNA polymorphisms have been associated with high production of fetal hemoglobin (HbF), although the molecular basis is not completely understood. In order to identify and characterize novel HbF-associated elements, we focused on five probands and their four families (from Egypt, Iraq and Iran) with thalassemia major (either β-IVSII-1 or β-IVSI-1) and unusual HbF elevation (>98 %), congenital or acquired after rejection of bone marrow transplantation, suggesting an anticipated favorable genetic background to high HbF expression. Methods: Patient recruitment, genomic DNA sequencing, western blotting, electrophoretic mobility shift assays, surface plasmon resonance (SPR) biospecific interaction analysis, bioinformatics analyses based on docking experiments. Results: A polymorphism of the Aγ-globin gene is here studied in four families with β-thalassemia (β-IVSII-1 and β-IVSI-1) and expressing unusual high HbF levels, congenital or acquired after rejection of bone marrow transplantation. This (G→A) polymorphism is present at position +25 of the Aγ-globin genes, corresponding to a 5′-UTR region of the Aγ-globin mRNA and, when present, is physically linked in chromosomes 11 of all the familiar members studied to the XmnI polymorphism and to the β-thalassemia mutations. The region corresponding to the +25(G→A) polymorphism of the Aγ-globin gene belongs to a sequence recognized by DNA-binding protein complexes, including LYAR (Ly-1 antibody reactive clone), a zinc-finger transcription factor previously proposed to be involved in down-regulation of the expression of γ-globin genes in erythroid cells. Conclusion: We found a novel polymorphism of the Aγ-globin gene in four families with β-thalassemia and high levels of HbF expression. Additionally, we report evidence suggesting that the Aγ-globin gene +25(G→A) polymorphism decreases the efficiency of the interaction between this sequence and specific DNA binding protein complexes. [ABSTRACT FROM AUTHOR]
Details
- Language :
- English
- ISSN :
- 11771062
- Volume :
- 20
- Issue :
- 2
- Database :
- Complementary Index
- Journal :
- Molecular Diagnosis & Therapy
- Publication Type :
- Academic Journal
- Accession number :
- 113838398
- Full Text :
- https://doi.org/10.1007/s40291-016-0187-2