Screening of the Single Nucleotide Polymorphisms in the Protamine 1 and 2 Genes of Korean Infertile Men.
- Author:
Hyoung Song LEE
1
;
Hye Won CHOI
;
Yong Seog PARK
;
Ju Tae SEO
;
Mi Kyoung KOONG
;
Jin Hyun JUN
Author Information
1. Laboratory of Reproductive Biology and Infertility, Sungkyunkwan University School of Medicine, Seoul, Korea. junjh55@hanmail.net
- Publication Type:Original Article
- Keywords:
Protamine 1 and 2 (PRM1 and PRM2);
Single nucleotide polymorphism (SNP);
Fertility;
Haploinsufficiency;
Spermatogenesis
- MeSH:
Amino Acids;
Animals;
Azoospermia;
Clinical Coding;
DNA;
Fertility;
Genotype;
Hand;
Haploinsufficiency;
Humans;
Infertility, Male;
Introns;
Male;
Mass Screening*;
Mice;
Nucleotides;
Oligospermia;
Phenotype;
Polymerase Chain Reaction;
Polymorphism, Single Nucleotide*;
Spermatogenesis
- From:Korean Journal of Fertility and Sterility
2005;32(3):279-286
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
OBJECTIVE: Although several genetic factors have been associated with defects in human spermatogenesis, the unambiguous causative genes have not been elucidated. The male infertility by haploinsufficiency of PRM1 or PRM2 has been reported in mouse model. The aim of this study was to identify the single nucleotide polymorphisms (SNPs) of PRM1 and PRM2, related to the genotype of Korean infertile men. METHODS: Genomic DNAs were extracted from peripheral bloods of infertile men with oligozoospermia or azoospermia, and analyzed using polymerase chain reaction (PCR) and direct sequencing. We carried out the direct sequencing analysis of amplified fragments in PRM1 (557 nucleotides from -42 to 515) and PRM2 (599 nucleotides from 49 to 648) genes, respectively. RESULTS: Three SNPs of coding region in the PRM1 gene was found in the analysis of 130 infertile men. However, the SNPs at a133g (aa 96.9%, ag 3.1% and gg 0.0%), c160a (cc 99.2%, ca 0.8% and aa 0.0%) and c321a (cc 56.9%, ca 35.4% and aa 7.7%) coded the same amino acids, in terms of silence phenotypes. On the other hand, as results of the PRM2 gene sequencing in 164 infertile men, only two SNPs, g398c (gg 62.2%, gc 31.1% and ga 6.7%) and a473c (aa 63.4%, ac 29.9% and cc 6.7%), were identified in the intron of the PRM2 gene. CONCLUSIONS: There was no mutation and significant SNPs on PRM1 and PRM2 gene in Korean infertile men. These results suggest that the PRM1 and PRM2 genes are highly conserved and essential for normal fertility of men.
