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Disorders of the synthesis of human fetal hemoglobin

Manca, Laura and Masala, Bruno Lucio (2008) Disorders of the synthesis of human fetal hemoglobin. IUBMB Life, Vol. 60 (2), p. 94-111. eISSN 1521-6551. Article.

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DOI: 10.1002/iub.4


Fetal hemoglobin (HbF), the predominant hemoglobin in the fetus, is a mixture of two molecular species (α2Gγ2 and α2Aγ2) that differ only at position 136 reflecting the products of two nonallelic γ-globin genes. At the time of birth, HbF accounts for ~70% of the total Hb. The Gγ:Aγ globin ratio in the HbF of normal newborn is 70:30 whereas in the trace amounts of HbF that is found in the adult it reverses to 40:60 because of a γ- to β-globin gene switch. Alterations of these ratios are indicative of a molecular defect at the level of the HbF synthesis. Qualitative hemoglobinopathies due to Gγ and Aγ chain structural variants, and quantitative hemoglobinopathies affecting the synthesis of HbF such as γ-thalassemias, duplications, triplications, and even sextuplications of the γ-globin genes, which may be detected in newborn blood lysates, have been described. Moreover, several pathological and nonpathological conditions affecting the β-globin gene cluster, such as β-thalassemia, sickle cell disease, δβ-thalassemia, and hereditary persistence of HbF syndromes, are characterized by the continued synthesis of γ-globin chains in the adult life. Studies of these natural mutants associated with increased synthesis of HbF in adult life have provided considerable insight into the understanding of the control of globin gene expression and Hb switching.

Item Type:Article
ID Code:1830
Uncontrolled Keywords:Genetics, hemoglobin, human molecular disease, molecular genetics, thalassemia
Subjects:Area 05 - Scienze biologiche > BIO/10 Biochimica
Divisions:001 Università di Sassari > 01 Dipartimenti > Scienze fisiologiche, biochimiche e cellulari
Copyright Holders:© 2008 IUBMB
Deposited On:18 Aug 2009 10:06

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