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Null allele frequencies at HLA-G locus in Iranian healthy subjects
Roghayeh Rahimi1, Ahmad Zavaran Hosseini, Fatemeh Yari
1Department of Immunology, Faculty of Medical Sciences, Tarbiat Modares University, Tehran, Iran.
Background:
HLA-G gene contains 15 alleles including a null allele, HLA-G*0105N. Previous studies have shown that HLA-G*0105N does not encode the complete HLA-G1 or HLA-G5 isoforms but encodes a functional HLA-G protein with the ability to inhibit NK cell cytolysis. Thus, although the biological functions of HLA-G1 and HLA-G5 proteins are abrogated, other isoforms such as HLA-G2 can replace their roles. Studies on the null allele of HLA-G gene could be useful in understanding the genetic variants of HLA-G alleles in ethnic groups.
Objective:
The goal of this research was to determine the frequency of HLA-G*0105N null allele in Iranian healthy subjects.
Methods:
The frequency of HLA-G*0105N null allele was evaluated in Iranian healthy subjects by PCR-RFLP method. Genomic DNA was isolated from the whole blood of 100 randomly selected, healthy, unrelated Iranian individuals using salting-out technique followed by PCR amplification of the exon 3 of HLA-G gene. PCR products were digested with PpUM-1 and the resulted fragments were analyzed using gel electrophoresis.
Results:
In this study the restriction enzyme digestion confirmed homozygous HLA-G*0105N null allele for 9 % of the population. Furthermore obtained results indicated that the total frequency of HLA-G*0105N null allele was 20 % in the studied population of Iran.
Conclusion:
The final data analysis showed that the total frequency of this allele in Iranian people was higher than other ethnic groups that have been studied so far.
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