Literature DB >> 21453056

IVSII-666 of human beta-globin gene: a polymorphic marker linked to codon 8(-AA) mutation.

Haleh Akhavan-Niaki1, Siamak Shafiezadeh Seresti, Beheshteh Asghari, Ali Banihashemi.   

Abstract

AIMS: IVSII-666 (C-T) is one of the polymorphic sites located in the second intron of the β-globin gene. Its polymorphism rate and relationship to a specific mutation are studied for the first time on 211 DNA samples of thalassemia trait patients living in Mazandaran province in North Iran using Ssp1 restriction enzyme. β-Globin haplotype determination at XmnI/(G)γ, HincII/3'Ψβ, HinfI/5'β, RsaI/5'β, and SspI/β sites was also performed by analysis of family members.
RESULTS: Nineteen different haplotypes were encountered in 211 unrelated thalassemia trait patients. One hundred twenty-seven patients (60.2%) were homozygous (+/+), 81 (38.4%) were heterozygous (+/-), and 3 (1.4%) were homozygous (-/-) for Ssp1 polymorphism. Of 24 mutant chromosomes negative for SspI, 16 were linked to mutation in codon 8(-AA). All codon 8(-AA) mutations were linked to the SspI-negative site.
CONCLUSION: The SspI site can be used as a marker for tracking either normal β-globin gene (11.9%) or mutant alleles at codon 8 during prenatal diagnosis.

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Year:  2011        PMID: 21453056     DOI: 10.1089/gtmb.2010.0242

Source DB:  PubMed          Journal:  Genet Test Mol Biomarkers        ISSN: 1945-0257


  1 in total

1.  Beta globin frameworks in thalassemia major patients from north iran.

Authors:  Haleh Akhavan-Niaki; Ali Banihashemi; Mandana Azizi
Journal:  Iran J Pediatr       Date:  2012-09       Impact factor: 0.364

  1 in total

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