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Genetic polymorphisms of KIR2DS4 gene among ethnic Hans from southern China / 中华医学遗传学杂志
Article in Chinese | WPRIM (Western Pacific) | ID: wpr-345333
Responsible library: WPRO
ABSTRACT
<p><b>OBJECTIVE</b>To study genetic polymorphisms of the KIR2DS4 gene among ethnic Hans from southern China.</p><p><b>METHODS</b>Genomic DNA was isolated from 306 unrelated individuals and amplified with KIR2DS4-specific PCR primers. KIR2DS4-positive samples were genotyped for the entire coding sequence by sequencing-based typing (SBT). Assignment of allelic genotypes was accomplished by using Assign 3.5 software. For samples with inconclusive SBT results, RT-PCR products covering the entire coding sequence of the KIR2DS4 gene were subjected to cloning and haplotype sequencing.</p><p><b>RESULTS</b>Among all tested samples, 297 were demonstrated to have carried the KIR2DS4 framework gene. For KIR2DS4-positive samples subjected to SBT for the entire coding sequences, no background was observed with the obtained sequences. Three of the seven identified alleles were of novel types, which were officially named by the KIR subcommittee of the World Health Organization Nomenclature Committee for Factors of HLA System. The observed frequencies for the 7 alleles were KIR2DS4*00101 (78.8%), *003 (10.5%), *004 (16.0%), *010 (23.2%), *017 (0.3%), *00105 (0.3%) and *018 (0.7%), respectively. Allele KIR2DS4*007 was not found. The overall frequency for normal cell-surface expression KIR2DS4 alleles including 2DS4*00101, *017 and *00105 was 79.4%, and that for non cell-surface expression alleles including 2DS4*003, *004, *010 and *018 was 50.4%. The ratio between the two was 1.61.</p><p><b>CONCLUSION</b>The present study has elucidated the allelic diversity of KIR2DS4 among ethnic Hans from southern China, which may provide valuable data for transplantation as well as studies on KIR-associated disease and evolution.</p>
Subject(s)
Full text: Available Health context: Sustainable Health Agenda for the Americas / SDG3 - Health and Well-Being Health problem: Goal 11: Inequalities and inequities in health / Target 3.8 Achieve universal access to health Database: WPRIM (Western Pacific) Main subject: Polymorphism, Genetic / Haplotypes / Base Sequence / China / Sequence Analysis, DNA / Asian People / Alleles / Receptors, KIR / Genotyping Techniques / Gene Frequency Type of study: Prognostic study Aspects: Equity and inequality Limits: Humans Country/Region as subject: Asia Language: Chinese Journal: Chinese Journal of Medical Genetics Year: 2017 Document type: Article
Full text: Available Health context: Sustainable Health Agenda for the Americas / SDG3 - Health and Well-Being Health problem: Goal 11: Inequalities and inequities in health / Target 3.8 Achieve universal access to health Database: WPRIM (Western Pacific) Main subject: Polymorphism, Genetic / Haplotypes / Base Sequence / China / Sequence Analysis, DNA / Asian People / Alleles / Receptors, KIR / Genotyping Techniques / Gene Frequency Type of study: Prognostic study Aspects: Equity and inequality Limits: Humans Country/Region as subject: Asia Language: Chinese Journal: Chinese Journal of Medical Genetics Year: 2017 Document type: Article
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