Human catalase gene polymorphism (CAT C-262T) and risk of male infertility

S Sabouhi1, Z Salehi, M H Bahadori

  • 1Department of Biology, Faculty of Sciences, University of Guilan, Rasht, Iran.

Andrologia
|January 25, 2014
PubMed

Insights

The catalase C-262T gene variant may offer protection against idiopathic male infertility. Specifically, the CAT-262T/T genotype appears to reduce susceptibility in men, warranting further investigation.

Area of Science:

  • Genetics
  • Reproductive Biology
  • Biochemistry

Background:

  • Infertility affects couples trying to conceive for over a year.
  • Reactive oxygen species (ROS) are implicated in various diseases.
  • Catalase is an antioxidant enzyme that neutralizes hydrogen peroxide (H2O2).

Purpose of the Study:

  • To investigate the association between catalase C-262T gene polymorphism and idiopathic male infertility.
  • To determine if specific catalase genotypes influence male infertility risk.

Main Methods:

  • Genomic DNA was extracted from leukocytes of 195 infertile men and 190 healthy controls.
  • Allele-specific PCR (AS-PCR) was used to determine genotype and allele frequencies.
  • Statistical analysis was performed to compare frequencies between groups.

Main Results:

  • Significant differences in genotype frequencies were observed between infertile men and healthy controls (P < 0.05).
  • The CAT-262T/T genotype was less prevalent in infertile subjects compared to controls.
  • The CAT-CC and CAT-CT genotypes were more prevalent in infertile men.

Conclusions:

  • The catalase C-262T polymorphism is associated with idiopathic male infertility.
  • The CAT-262T/T genotype may confer a protective effect against male infertility.
  • Larger studies are needed to confirm these findings and their clinical implications.

Related Concept Videos

X-Inactivation01:58

X-Inactivation

The human X chromosome contains over ten times the number of genes as in the Y chromosome. Since males have only one X chromosome, and females have two, one might expect females to produce twice as many of the proteins, with undesirable results.
38.9K
Incomplete Dominance01:43

Incomplete Dominance

Gregor Mendel's work (1822 - 1884) was primarily focused on pea plants. Through his initial experiments, he determined that every gene in a diploid cell has two variants called alleles inherited from each parent. He suggested that amongst these two alleles, one allele is dominant in character and the other recessive. The combination of alleles determines the phenotype of a gene in an organism.
19.0K
Mutations01:39

Mutations

Overview
66.8K
Pharmacogenetics of Phase I Enzymes: Cytochrome P450 Isozymes01:28

Pharmacogenetics of Phase I Enzymes: Cytochrome P450 Isozymes

Cytochrome P450 (CYP450) enzymes are a superfamily of heme-containing monooxygenases that play a pivotal role in Phase I drug metabolism by catalyzing oxidation and reduction reactions.These enzymes transform lipophilic xenobiotics into more hydrophilic metabolites, facilitating subsequent Phase II conjugation and eventual excretion. The CYP450 family is classified into families (e.g., CYP1–CYP3) and subfamilies (e.g., CYP2A, CYP2C), based on amino acid sequence homology.CYP450...
338
Animal Mitochondrial Genetics02:59

Animal Mitochondrial Genetics

Among all the organelles in an animal cell, only mitochondria have their own independent genomes. Animal mitochondrial DNA is a double-stranded, closed-circular molecule with around 20,000 base pairs. Mitochondrial DNA is unique in that one of its two strands, the heavy, or H, -strand is guanine rich, whereas the complementary strand is cytosine rich and called the light, or L, -strand. Compared to nuclear DNA, mitochondrial DNA has a very low percentage of non-coding regions and is marked by...
7.8K
Infertility in Males01:23

Infertility in Males

Male infertility affects millions of couples worldwide, arising from various factors that impact different stages of the reproductive process. An endocrine imbalance resulting from conditions like hypogonadism, Klinefelter syndrome, or pituitary disorders can disrupt hormone levels and reduce sperm production. Testicular defects, such as tumors, cryptorchidism, atrophic testes, abnormal sperm morphology, and low sperm count or motility, may arise due to genetic factors, structural...
665