Heterozygosis deficit of polymorphic markers linked to the β-globin gene cluster region in the Iranian population

Moradi, Tahereh and Vallian, Reihaneh and Fazeli, Zahra and Haghighatnia, Asieh and Vallian, Sadeq (2015) Heterozygosis deficit of polymorphic markers linked to the β-globin gene cluster region in the Iranian population. Iranian Journal of Basic Medical Sciences, 18 (6). pp. 571-575.

IJBMS_Volume 18_Issue 6_Pages 571-575.pdf

Download (344kB) | Preview
Official URL: http://ijbms.mums.ac.ir/article_4531.html


Objective(s): Iran is considered as one of the high-prevalence areas for β-thalassemia with a rate of about 10 carrier frequency. Molecular diagnosis of the disease is performed both by direct sequencing and indirectly by the use of polymorphic markers present in the beta globin gene cluster. However, to date there is no reliable information on the application of the markers in the Iranian population. Here we report the results of an extended molecular analysis of five RFLP markers, XmnI, HindIIIA, HindIIIG, RsaI and HinfI, located within the β-globin gene cluster region in four subpopulations of Iran. Materials and Methods:A total of 552 blood samples taken from the Iranian subpopulations including Isfahan, Chaharmahal-O-Bakhtiari, Khuzestan and Hormozgan were genotyped using PCR-RFLP and sequencing. The allele frequency, the expected and observed heterozygosity, and Shannon's information index (I) of these markers were calculated. Results:Distribution of the allele frequencies for XmnI, HindIIIA, HindIIIG, RsaI and HinfI polymorphic markers did not differ significantly among the subpopulations examined. Overall observed heterozygosity ranged from 0.1706 for HindIIIA to 0.4484 for RsaI. The Shannon index was Conclusion:The results suggested that genotyping of these markers is not informative enough once used as single markers for prenatal diagnosis and carrier detection of β-thalassemia in the Iranian population. However, haplotyping of these markers may provide more useful data in linkage analysis and prenatal diagnosis as well as carrier detections for β-thalassemia in Iranians.

Item Type: Article
Subjects: QT physiology
Divisions: Journals > Iranian J Basic Medical Sciences
Depositing User: ijbms ijbms
Date Deposited: 03 Oct 2017 13:16
Last Modified: 03 Oct 2017 13:16
URI: http://eprints.mums.ac.ir/id/eprint/7342

Actions (login required)

View Item View Item