Please use this identifier to cite or link to this item: https://scholarbank.nus.edu.sg/handle/10635/111765
Title: A rapid HLA-DRB1*04 subtyping method using PCR and DNA heteroduplex generators
Authors: Savage, D.A. 
Tang, J.P. 
Wood, N.A.P.
Evans, J.
Bidwell, J.L.
Wee, J.L.K.
Oei, A.A. 
Hui, K.M. 
Keywords: DNA heteroduplex generator
HLA-DRB1*04
PCR-restriction fragment length polymorphism
PCR-sequence-specific oligonucleotide
PCR-sequence-specific primer
PCR-single strand conformation polymorphism
Polymerase chain reaction
Issue Date: 1996
Citation: Savage, D.A., Tang, J.P., Wood, N.A.P., Evans, J., Bidwell, J.L., Wee, J.L.K., Oei, A.A., Hui, K.M. (1996). A rapid HLA-DRB1*04 subtyping method using PCR and DNA heteroduplex generators. Tissue Antigens 47 (4) : 284-292. ScholarBank@NUS Repository.
Abstract: We describe here a rapid polymerase chain reaction (PCR)-based method for the identification of HLA-DRB1*0401-*0412 alleles. The method is based on the generation of specific DNA heteroduplex patterns between PCR products derived from selective group-specific amplification of the various DRB1*04 alleles and PCR products derived from two synthetic DNA heteroduplex generator (DHG) molecules following non-denaturing polyacrylamide minigel electrophoresis. One DHG was designed to detect DRB1*0401, *0405, *0407, *0408, and *0409 alleles, whilst the other was designed to detect DRB1*0402, *0403, *0404, *0406, *0410, *0411, and *0412 alleles. Characteristic heteroduplex patterns were obtained for all DRB1*04 alleles tested both in homozygous and heterozygous situations. Both DHG and PCR-SSP (sequence-specific primer) typing were performed on 41 DRB1*04 positive DNAs from Singaporean Chinese blood donors and complete concordance in results was obtained. HLA-DRB1*0403, *0405, and *0406 were found to account for 95% of the DRB1*04 alleles in the population studied. The DHG technique described is technically simple and rapid since it essentially involves only two PCR amplifications per individual subtyping. The technique is particularly useful for resolving DRB1*04 combinations which are indistinguishable by PCR-SSO (sequence-specific oligonucleotide) or PCR-SSP subtyping. © Munksgaard, 1996.
Source Title: Tissue Antigens
URI: http://scholarbank.nus.edu.sg/handle/10635/111765
ISSN: 00012815
Appears in Collections:Staff Publications

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