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KMID : 0617319950050010111
Journal of Pharmacetical Sceiences Ewha Womans University
1995 Volume.5 No. 1 p.111 ~ p.116
Polymerase Chain Reaction and Denaturing Gradient Gel Electrophoresis for Screening New Alleles in HLA-DQ¥á
Nam, Hyun Suk
Kim, Kyun Eun/Lee, Kong-Joo/Kim, Eun-Hee
Abstract
The sequences of HLA-DQ¥á alleles are relatively polymorphic and HLA-DQ typing methods developed to date sometimes fail to discern minute base differences among alleles. Thus this study tried to apply the denaturing gradient gel electrophorcsis (DGGE) method for screening new alleles in HLA-DQ¥á typing. DGGE is a method in which double stranded, equal length DNA molecules with one base difference can be resuolved because of their different melting behavior. 242 bp of the second exon of HLA-DQ¥á gene was amplified by polymerase chain reaction with a GC-clamped printer and subsequently subjected to DGGE. The optimum polymerase chain reaction condition for HLA-DQ¥á with a 39 bp GC-clamped primer was investigated. A computer algorithm to simulate melting behavior was used in order to optimize DGGE condition. Also extensive experimental adjustment was done regarding the denaturant gradient range and gel running time. Computational simulation and experimental results were compared. Tentative new alleles were discovered among alleles which were typed as the same alleles using the sequence specific oligonucleotide probe method. This study demonstrated the superior sensitivity of DGGE as an HLA-DQ¥á allele typing method.
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