Literature DB >> 2430259

Genetic control of the proportion of gamma chains of human fetal haemoglobin.

M Arbane, L Morle, E Dessi, P Rouyer-Fessard, F Morle, J Feingold, A Cao, Y Beuzard.   

Abstract

The relative proportions of gamma chains of human fetal haemoglobin G gamma, A gamma 75 Ileu (A gamma I) and A gamma 75 Thr (A gamma T) were investigated in homogeneous populations of patients in Algeria exhibiting sickle cell disease and in patients in Algeria and Sardinia with beta-thalassaemia. The restriction site haplotypes within the beta gene cluster were known. The results suggest a tight genetic regulation of the G gamma/A gamma + G gamma ratio (G gamma ratio) which is associated with the G gamma Hind III site of polymorphism (p less than 0.0001). From the present results and those in the literature the high G gamma ratio is associated with the presence of 3 polymorphic restriction sites: Xmn1 5' to the G gamma gene, Hind III in the G gamma IVS II and Hinc II in the psi beta gene. Familial studies showed that the expression of the A gamma alleles is genetically determined. The wide variation of the A gamma T/A gamma T + A gamma I ratio (A gamma ratio) between families is most probably related to the various haplotypes bearing the A gamma I alleles.

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Year:  1986        PMID: 2430259

Source DB:  PubMed          Journal:  Nouv Rev Fr Hematol


  1 in total

1.  Transfusion-independent β(0)-thalassemia after bone marrow transplantation failure: proposed involvement of high parental HbF and an epigenetic mechanism.

Authors:  Katia Paciaroni; Guido Lucarelli; Fabrizio Martelli; Anna Rita Migliaccio; Marieke von Lindern; Joseph Borg; Nynke Gillemans; Thamar B van Dijk; Sjaak Philipsen
Journal:  Am J Blood Res       Date:  2014-09-05
  1 in total

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