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The CAG repeat polymorphism of mitochondrial polymerase gamma (POLG) is associated with male infertility in Tunisia
Author(s) -
BakloutiGargouri S.,
Ghorbel M.,
Chakroun N.,
Sellami A.,
Fakhfakh F.,
AmmarKeskes L.
Publication year - 2012
Publication title -
andrologia
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.633
H-Index - 59
eISSN - 1439-0272
pISSN - 0303-4569
DOI - 10.1111/j.1439-0272.2010.01139.x
Subject(s) - male infertility , biology , genotype , infertility , mitochondrial dna , genotyping , genetics , azoospermia , andrology , population , sperm , gene , medicine , pregnancy , environmental health
Summary Male fertility largely depends on sperm quality, which may be affected by environmental and genetic factors. Recent data emphasised the implication of the polymorphism of mitochondrial DNA polymerase gamma (POLG) CAG repeats in male infertility. In this report, we explored a possible role of the (POLG) gene polymorphism in male infertility in Tunisian men. The polymorphic CAG repeat in the nuclear POLG gene was studied in 339 male subjects (216 patients with infertility (69 azoospermic, 115 oligoasthenoteratospermic and 32 normospermic) and 123 fertile) after DNA amplification by PCR, followed by genotyping using an automatic sequencer. The heterozygous and the homozygous mutant genotypes (10/≠10 and ≠10/≠10) were significantly more frequent among infertile patients than among fertile controls (11.2% versus 1.6%, P = 1.3 × 10 −3 and 4.6% versus 0.8%, P = 4.2 × 10 −7 respectively). We also found a significant difference between the frequencies of 10/≠10 genotype in azoospermic (4.4%) and in oligoasthenoteratospermic (15.6%) infertile patients ( P = 2.6 × 10 −2 ). However, the homozygous mutant genotype (≠10/≠10) was seen at similar frequencies in azoospermic, normospermic and oligoasthenospermic men (4.4%, 3.1% and 5.2% respectively). Under our conditions, the findings showed an association between POLG CAG repeat polymorphism and male infertility in Tunisian population.