Study of the Allelic Frequency on Polymorphic Loci in the Short Arm of Chromosome 3 in Normal Koreans.
- Author:
Young Jin SON
1
;
In Who KIM
;
Jin Han YOON
Author Information
1. Department of Urology, Dong-A University College of Medicine, Pusan, Korea.
- Publication Type:Original Article
- Keywords:
renal cell carcinoma;
polymerase chain reaction
- MeSH:
Arm*;
Carcinogenesis;
Carcinoma, Renal Cell;
Chromosomes, Human, Pair 3*;
Female;
Genes, Tumor Suppressor;
Genetic Diseases, Inborn;
Genetic Loci;
Humans;
Male;
Polymerase Chain Reaction;
Polymorphism, Restriction Fragment Length
- From:Korean Journal of Urology
1996;37(10):1087-1092
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
The results of allelic frequency of polymorphic loci in the short arm of chromosome 3 in normal Koreans are shown using a polymerase chain reaction (PCR) based restriction fragment length polymorphism analysis on blood samples of 20 males and 20 females without any tumor or hereditary diseases. The allelic frequency of two loci, D3S2 (MspI) and D3F15S2 (Hind III ) was quite different between renal cell carcinoma in Koreans and Caucasians, but THRB (MspI) locus was similar This suggests the importance of determining specific loci to Koreans. The study of tumor suppressor gene on these genetic loci due to D3S2 (MspI) and THRB (EcoRI) loci showed high constitutional heterozygosity, contrast to D3F15S2 (Hind III), THRB (BamHI) and THRB (MspI) loci where low constitutional heterozygosity were seen. Therefore, the study of tumor suppressor gene should be directed to investigate. This study showed the allelic distribution of Koreans differing from Caucasians and the genetic locus with the high frequency of heterozygosity among the polymorphic loci comparable to Koreans were due to the difference of heterozygosity frequency according to genetic loci. Therefore, the author thinks that the need for the detection of specific genetic loci for Koreans to study the correlation among many cases for classifying the tumorigenesis and active research should be initiated to find other genetic locus related to multi-step tumorigenesis.
