Killer-cell immunoglobulin-like receptor genes linkage disequilibrium analysis in population of Vojvodina
Killer Immunoglobulin-like Receptors (KIRs) form a group of regulatory molecules that modulate cytolytic activity of natural killer cells and T cells through interaction with specific human leukocyte antigen (HLA) molecules on target cells. KIRs are encoded by the family of 16 homologous genes that...
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Published in | Genetika (Beograd) Vol. 47; no. 2; pp. 439 - 450 |
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Main Authors | , |
Format | Journal Article |
Language | English |
Published |
2015
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Online Access | Get full text |
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Summary: | Killer Immunoglobulin-like Receptors (KIRs) form a group of regulatory
molecules that modulate cytolytic activity of natural killer cells and T
cells through interaction with specific human leukocyte antigen (HLA)
molecules on target cells. KIRs are encoded by the family of 16 homologous
genes that vary substantially between haplotypes and display sequence
polymorphism with allelic variation that also contributes to diversity within
the complex. The aim of the study is to estimate two locus linkage
disequilibrium for 16 KIR loci. In this study, we report the evaluation of
KIR gene content, allele, haplotype and genotype frequencies in 175 unrelated
healthy individuals from Vojvodina who were KIR typed by polymerase chain
reaction-sequence specific primers genotyping assay. The linkage
disequilibrium (LD) was studied at the structural level (presence or absence
of 16 KIR genes). Our results revealed that linkage disequilibrium is present
between telomeric gene pairs KIR2DL1~KIR2DL4, KIR2DP1~KIR2DL4,
KIR2DP1~KIR3DL1, KIR2DL1~KIR3DL2, KIR2DP1~KIR3DL2, KIR2DL4~KIR3DL1,
KIR2DL4~KIR2DS4, KIR2DL4~KIR3DL2 where (r2=1), but positive association
between KIR genes, with higher observed than expected haplotype frequencies
were observed for KIR3DS1~KIR2DS1 and KIR2DL5~KIR2DS1 pair of genes
(r2=0.646) and (r2=0.371), respectively. Thirty-eight different genotypes
were identified, where 12% of the individuals have unique genotype, present
in only one person. Our results will help to understand the genetic
background of the Vojvodina population, in illustrating the population
migration events in the northern part of Serbia, in explaining the extensive
genetic admixture amongst the different ethnic groups of the region and also
in KIR-related disease studies.
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 0534-0012 1820-6069 |
DOI: | 10.2298/GENSR1502439V |