STUDY OF THREE SINGLE NUCLEOTIDE POLYMORPHISMS IN THE SLC6A14 GENE IN ASSOCIATION WITH MALE INFERTILITY
Noveski P1, Mircevska M1, Plaseski T2, Peterlin B3, Plaseska-Karanfilska D1,*
*Corresponding Author: Dijana Plaseska-Karanfilska, M.D., Ph.D., Research Centre for Genetic Engineering and Biotechnology “Georgi D. Efremov,” Macedonian Academy of Sciences and Arts, Krste Misirkov 2, 1000 Skopje, Republic of Macedonia. Tel. +389-2-3235-410. Fax: +389-2-3115-434. E-mail: dijana@manu.edu.mk
page: 61

RESULTS

Because we studied only male subjects and the SLC6A14 gene is on the X chromosome, we calculated only allelic and haplotype frequencies and compared results within populations. When we analyzed allelic frequencies, only the rs2011162 SNP showed difference in the distribution among infertile patients and fertile men. In both Macedonians and Slovenians, the rs2011162(G) allele was present with lower frequencies in infertile patients (Table 3). However, statistical significance was obtained only for the Macedonian population [p = 0.0439; odds ratio (OR) = 1.69; 95% confidence interval (95% CI) = 1.01-2.81]. Five different haplotypes for rs2312054, rs2071877 and rs2011162 were observed in both populations: ACG, ATC, TCG, ACC and TTC (Table 3). Only one haplotype (ACG) showed statistically significant difference in distribution, but only in Macedonian men. It was less frequent (36.6%) in infertile Macedonian men than in fertile Macedonian controls (52.0%) [p = 0.0144; OR = 1.87; 95% CI = 1.13-3.11]. Analysis of the effect of the rs2011162 alleles on RNA secondary structure showed significant structural change in the alternative allele in comparison to the wild type allele when using Mode 1 for analysis (p = 0.0783) (Figure 2).



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