Two new β + -thalassemia mutation [ β -56 (G → C); HBBc. −106 G → C ] and [ β −83 (G → A); HBBc. −133 G → A ] described among the Tunisian population

Kais Douzi; Imen Moumni; Amine Zorai; Maha Ben Mustapha; Ikbel Mosbahi Ben Mansour; Chaouachi Dorra; Abbes Salem

doi:10.1002/ajhb.22695

Two new β + -thalassemia mutation [ β -56 (G → C); HBBc. −106 G → C ] and [ β −83 (G → A); HBBc. −133 G → A ] described among the Tunisian population

Kais Douzi ^{1, *} Imen Moumni ¹ Amine Zorai ¹ Maha Ben Mustapha ¹ Ikbel Mosbahi Ben Mansour ¹ Chaouachi Dorra ¹ Abbes Salem ¹

* Auteur correspondant

1 LR11IPT07 - Laboratoire d'hématologie moléculaire et cellulaire

Abstract : ObjectivesDifferent thalassemia mutations have been reported in various ethnic groups and geographical regions in Tunisia. In the present study, we have investigated two rare beta(+)-thalassemia mutations, that have not previously been reported in the Tunisian population [beta -56 (G>C); HBBc. -106 G>C] and [beta -83 (G>A); HBBc. -133 G>A]. MethodsThe whole beta-globin gene was directly sequenced, and haplotype analysis was conducted through a PCR/RFLP method. Results: Two new mutations were identified for the first time in Tunisia. They are located within the promoter region of beta-globin gene at position -56 (G>C) and -83 (G>A). Linkage analysis using beta-globin gene cluster haplotypes showed that these two mutations were associated with Mediterranean beta-haplotype IX [-+-++++] and framework 2 (FW2) [CCTCT]. ConclusionsThe two newly described mutations lead to the beta(+)-thalassemia among Tunisian patients. The haplotype analysis and framework assignment have helped to identify the chromosomal background associated with these mutations, and determine their origin and spread. Am. J. Hum. Biol. 27:716-719, 2015. (c) 2015 Wiley Periodicals, Inc.

Type de document :

Article dans une revue

American Journal of Human Biology, Wiley, 2015, 27 (5), pp.716 - 719. 〈10.1002/ajhb.22695〉

Domaine :

Sciences du Vivant [q-bio]

Sciences du Vivant [q-bio] / Médecine humaine et pathologie / Hématologie

Sciences du Vivant [q-bio] / Génétique / Génétique des populations [q-bio.PE]

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https://hal-riip.archives-ouvertes.fr/pasteur-01375041
Contributeur : Institut Pasteur Tunis <>
Soumis le : dimanche 2 octobre 2016 - 20:02:28
Dernière modification le : lundi 5 février 2018 - 15:22:12

Two new β + -thalassemia mutation [ β -56 (G → C); HBBc. −106 G → C ] and [ β −83 (G → A); HBBc. −133 G → A ] described among the Tunisian population

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Two new β + -thalassemia mutation [ β -56 (G → C); HBBc. −106 G → C ] and [ β −83 (G → A); HBBc. −133 G → A ] described among the Tunisian population

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