Genomic characterisation of the Jk(a-b-) phenotype in Thai blood donors

Background. The Kidd (JK) blood group antigens are encoded by the JK gene. The rare Jk(a-b-) phenotype can be caused by homozygosity for a silent JK allele. Currently, JK null alleles have been identified among different populations; however, information on its presence among Thais is not available...

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Main Authors: Pramote Sriwanitchrak, Kanchana Sriwanitchrak, Jintana Tubrod, Pawinee Kupatawintu, Chollanot Kaset, Oytip Nathalang
Other Authors: Thammasat University
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Published: 2018
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Online Access:https://repository.li.mahidol.ac.th/handle/123456789/14806
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spelling th-mahidol.148062018-06-11T12:11:19Z Genomic characterisation of the Jk(a-b-) phenotype in Thai blood donors Pramote Sriwanitchrak Kanchana Sriwanitchrak Jintana Tubrod Pawinee Kupatawintu Chollanot Kaset Oytip Nathalang Thammasat University Mahidol University Thai Red Cross Agency Medicine Background. The Kidd (JK) blood group antigens are encoded by the JK gene. The rare Jk(a-b-) phenotype can be caused by homozygosity for a silent JK allele. Currently, JK null alleles have been identified among different populations; however, information on its presence among Thais is not available. Materials and methods. Screening for the Jk(a-b-) phenotype by the urea lysis test was performed in 25,340 blood samples from Thai blood donors. The Jk(a-b-) phenotypes were confirmed by an indirect antiglobulin test (IAT). Additionally, polymerase chain reaction amplification and sequence analysis of the JK gene were performed using previously described methods. Results. Five samples were confirmed as having a Jk(a-b-) phenotype by a urea lysis test and IAT; four of these samples were investigated. Two samples of JK*02 alleles were homozygous for a g > a mutation at the 3′ acceptor splice site of intron 5 of the JK gene, as in previous studies in Asians and Polynesians. Moreover, one sample of JK*02 alleles was homozygous for an 896G > A mutation at exon 9 (Gly299Glu), as in a previous study in Polynesians. Interestingly, missense dual mutations of JK*01 alleles from a female blood donor were identified. The first mutation was 956C > T (Thr319Met) in exon 10, as in a recent study in African-Americans. The second mutation was 130G > A (Glu44Lys) at exon 4, as in previous studies among Caucasians. Conclusion. There are various different molecular bases of the Jk(a-b-) phenotype. This is the first report of JK null alleles among Thais. The information presented in this study could be beneficial in planning genotyping strategies for blood donors and patients. © SIMTI Servizi Srl. 2018-06-11T05:11:19Z 2018-06-11T05:11:19Z 2012-05-08 Article Blood Transfusion. Vol.10, No.2 (2012), 181-185 10.2450/2011.0038-11 17232007 2-s2.0-84860530022 https://repository.li.mahidol.ac.th/handle/123456789/14806 Mahidol University SCOPUS https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84860530022&origin=inward
institution Mahidol University
building Mahidol University Library
continent Asia
country Thailand
Thailand
content_provider Mahidol University Library
collection Mahidol University Institutional Repository
topic Medicine
spellingShingle Medicine
Pramote Sriwanitchrak
Kanchana Sriwanitchrak
Jintana Tubrod
Pawinee Kupatawintu
Chollanot Kaset
Oytip Nathalang
Genomic characterisation of the Jk(a-b-) phenotype in Thai blood donors
description Background. The Kidd (JK) blood group antigens are encoded by the JK gene. The rare Jk(a-b-) phenotype can be caused by homozygosity for a silent JK allele. Currently, JK null alleles have been identified among different populations; however, information on its presence among Thais is not available. Materials and methods. Screening for the Jk(a-b-) phenotype by the urea lysis test was performed in 25,340 blood samples from Thai blood donors. The Jk(a-b-) phenotypes were confirmed by an indirect antiglobulin test (IAT). Additionally, polymerase chain reaction amplification and sequence analysis of the JK gene were performed using previously described methods. Results. Five samples were confirmed as having a Jk(a-b-) phenotype by a urea lysis test and IAT; four of these samples were investigated. Two samples of JK*02 alleles were homozygous for a g > a mutation at the 3′ acceptor splice site of intron 5 of the JK gene, as in previous studies in Asians and Polynesians. Moreover, one sample of JK*02 alleles was homozygous for an 896G > A mutation at exon 9 (Gly299Glu), as in a previous study in Polynesians. Interestingly, missense dual mutations of JK*01 alleles from a female blood donor were identified. The first mutation was 956C > T (Thr319Met) in exon 10, as in a recent study in African-Americans. The second mutation was 130G > A (Glu44Lys) at exon 4, as in previous studies among Caucasians. Conclusion. There are various different molecular bases of the Jk(a-b-) phenotype. This is the first report of JK null alleles among Thais. The information presented in this study could be beneficial in planning genotyping strategies for blood donors and patients. © SIMTI Servizi Srl.
author2 Thammasat University
author_facet Thammasat University
Pramote Sriwanitchrak
Kanchana Sriwanitchrak
Jintana Tubrod
Pawinee Kupatawintu
Chollanot Kaset
Oytip Nathalang
format Article
author Pramote Sriwanitchrak
Kanchana Sriwanitchrak
Jintana Tubrod
Pawinee Kupatawintu
Chollanot Kaset
Oytip Nathalang
author_sort Pramote Sriwanitchrak
title Genomic characterisation of the Jk(a-b-) phenotype in Thai blood donors
title_short Genomic characterisation of the Jk(a-b-) phenotype in Thai blood donors
title_full Genomic characterisation of the Jk(a-b-) phenotype in Thai blood donors
title_fullStr Genomic characterisation of the Jk(a-b-) phenotype in Thai blood donors
title_full_unstemmed Genomic characterisation of the Jk(a-b-) phenotype in Thai blood donors
title_sort genomic characterisation of the jk(a-b-) phenotype in thai blood donors
publishDate 2018
url https://repository.li.mahidol.ac.th/handle/123456789/14806
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