Article

Genotype patterns and characteristics of PRNP in the Korean population.

Korea Centers for Disease Control and prevention, Division of Arboviruses, Center for Immunology & Pathology, National Institute of Health, Gangoe-myeon, Cheongwon-gun, Chungcheongbuk-do 363-951, Korea (South), Republic of.
Prion (impact factor: 2.85). 09/2012; 6(4):375-82. DOI:10.4161/pri.20195 pp.375-82
Source: PubMed

ABSTRACT Creutzfeldt-Jakob disease (CJD), included in the human transmissible spongiform encephalopathies (TSE), is widely known to be caused by an abnormal accumulation of misfolding prion protein in the brain. Human prion protein gene (PRNP) is mapped in chromosome 20p13 and many single nucleotide polymorphisms (SNPs) in PRNP have been discovered. However, the functionality of SNPs in PRNP is yet unclear, though several SNPs have been known as important mutation related with susceptibility human prion diseases. Our aim is to identify specific genotype patterns and characteristics in the PRNP genomic region and to understand susceptibility among Korean discriminated prion disease patients, suspected CJD patients and the KARE data group. Here, we have researched genotypes and SNPs allele frequencies in PRNP in discriminated prion disease patients group (n = 22), suspected prion diseases patients group (n = 163) and the Korea Association REsource (KARE) data group (n = 296) in Korea. The sequencing regions were promoter region, exon1 and exon2 with their junction parts among 481 samples. A total of 25 SNPs were shown in this study. Nucleotide frequencies of all SNPs are exceedingly tended to bias toward dominant homozygote types except in rs2756271. Genotype frequencies at codon 129 and 219 coding region were similar with previous studies in Korea and Japan. Pathogenic mutations such as 102P/L, 200E/K and 203V/I were observed in discriminated CJD patients group, and 180V/I and 232M/R were shown in suspected prion disease patients group and the KARE data group. A total of 10 SNPs were newly identified, six in the promoter region, one in exon 2 and three in the 3' UTR. The strong and unique linkage disequilibrium (D' = 0.94, r ( 2) = 0.89) was observed between rs57633656 and rs1800014 which is located in codon 219 coding region. We expect that these data can be provided to determine specific susceptibility and a protective factor of prion diseases not only in Koreans but also in East Asians.

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Keywords

219 coding region
 
CJD patients
 
codon 219 coding region
 
discriminated CJD patients group
 
exon 2
 
exon2
 
Human prion protein gene
 
human transmissible spongiform encephalopathies
 
KARE data group
 
Korea Association REsource
 
Korean discriminated prion disease patients
 
misfolding prion protein
 
prion diseases
 
prion diseases patients group
 
PRNP genomic region
 
promoter region
 
sequencing regions
 
SNPs allele frequencies
 
specific genotype patterns
 
susceptibility human prion diseases
 

Sol Moe Lee