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 - Archive ouverte HAL Access content directly
Journal Articles American Journal of Human Biology Year : 2015

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

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.

Dates and versions

pasteur-01375041 , version 1 (02-10-2016)

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Kais Douzi, Imen Moumni, Amine Zorai, Maha Ben Mustapha, Ikbel Mosbahi Ben Mansour, et al.. 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. American Journal of Human Biology, 2015, 27 (5), pp.716 - 719. ⟨10.1002/ajhb.22695⟩. ⟨pasteur-01375041⟩

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