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The association between TNP2 gene polymorphisms and Iranian infertile men with varicocele: A case-control study

BACKGROUND: Numerous researches have provided great evidence that revealed the relationship between varicocele and sperm DNA damage. OBJECTIVE: Because of the crucial role of nuclear transition proteins (TPs) in sperm DNA condensation and integrity, this case-control study was designed to study TNP2...

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Autores principales: Heidari, Mohammad Mehdi, Danafar, Amirhossein, Moezzi, Fahime, Khatami, Mehri, Talebi, Ali Reza
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Knowledge E 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6745086/
https://www.ncbi.nlm.nih.gov/pubmed/31583373
http://dx.doi.org/10.18502/ijrm.v17i8.4821
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author Heidari, Mohammad Mehdi
Danafar, Amirhossein
Moezzi, Fahime
Khatami, Mehri
Talebi, Ali Reza
author_facet Heidari, Mohammad Mehdi
Danafar, Amirhossein
Moezzi, Fahime
Khatami, Mehri
Talebi, Ali Reza
author_sort Heidari, Mohammad Mehdi
collection PubMed
description BACKGROUND: Numerous researches have provided great evidence that revealed the relationship between varicocele and sperm DNA damage. OBJECTIVE: Because of the crucial role of nuclear transition proteins (TPs) in sperm DNA condensation and integrity, this case-control study was designed to study TNP2 gene nucleotide variations in Iranian patients with varicocele. MATERIALS AND METHODS: PCR-SSCP and DNA sequencing were used to search for mutations in exons 1 & 2 of the TNP2 gene in 156 infertile patients with varicocele and 150 fertile men. RESULTS: The results of sequencing showed three variants at positions c.301C░>░T (p.R101C), c.391C░>░T (p.R131░W), and g.IVS1-26G░>░C (rs8043625) of TNP2 gene. It was found that varicocele risk in men who have the CC genotype of g.IVS1-26G░>░C SNP is higher than those who don't have these genotypes (according to Co-dominant model, Dominant model, Recessive model, and Over-dominant model). The haplotype-based analysis showed that (C/C/T) and (C/T/T) haplotypes were a risk factor of in patients with varicocele compared to controls (OR░=░3.278, p░=░0.000 and OR░=░9.304, p░=░0.038, respectively). CONCLUSION: Because of the significant difference in the genotype and allele frequencies of g.IVS1-26G░>░C SNP in the intronic region of TNP2 in patients with varicocele compared with controls and also because of the high conservation of this SNP position during evolution, this SNP may be involved in some important processes associated with the expression of this gene like mRNA splicing, but the exact mechanism is not clear.
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spelling pubmed-67450862019-10-03 The association between TNP2 gene polymorphisms and Iranian infertile men with varicocele: A case-control study Heidari, Mohammad Mehdi Danafar, Amirhossein Moezzi, Fahime Khatami, Mehri Talebi, Ali Reza Int J Reprod Biomed Original Article BACKGROUND: Numerous researches have provided great evidence that revealed the relationship between varicocele and sperm DNA damage. OBJECTIVE: Because of the crucial role of nuclear transition proteins (TPs) in sperm DNA condensation and integrity, this case-control study was designed to study TNP2 gene nucleotide variations in Iranian patients with varicocele. MATERIALS AND METHODS: PCR-SSCP and DNA sequencing were used to search for mutations in exons 1 & 2 of the TNP2 gene in 156 infertile patients with varicocele and 150 fertile men. RESULTS: The results of sequencing showed three variants at positions c.301C░>░T (p.R101C), c.391C░>░T (p.R131░W), and g.IVS1-26G░>░C (rs8043625) of TNP2 gene. It was found that varicocele risk in men who have the CC genotype of g.IVS1-26G░>░C SNP is higher than those who don't have these genotypes (according to Co-dominant model, Dominant model, Recessive model, and Over-dominant model). The haplotype-based analysis showed that (C/C/T) and (C/T/T) haplotypes were a risk factor of in patients with varicocele compared to controls (OR░=░3.278, p░=░0.000 and OR░=░9.304, p░=░0.038, respectively). CONCLUSION: Because of the significant difference in the genotype and allele frequencies of g.IVS1-26G░>░C SNP in the intronic region of TNP2 in patients with varicocele compared with controls and also because of the high conservation of this SNP position during evolution, this SNP may be involved in some important processes associated with the expression of this gene like mRNA splicing, but the exact mechanism is not clear. Knowledge E 2019-09-03 /pmc/articles/PMC6745086/ /pubmed/31583373 http://dx.doi.org/10.18502/ijrm.v17i8.4821 Text en Copyright © 2019 Mohammad Mehdi Heidari et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Original Article
Heidari, Mohammad Mehdi
Danafar, Amirhossein
Moezzi, Fahime
Khatami, Mehri
Talebi, Ali Reza
The association between TNP2 gene polymorphisms and Iranian infertile men with varicocele: A case-control study
title The association between TNP2 gene polymorphisms and Iranian infertile men with varicocele: A case-control study
title_full The association between TNP2 gene polymorphisms and Iranian infertile men with varicocele: A case-control study
title_fullStr The association between TNP2 gene polymorphisms and Iranian infertile men with varicocele: A case-control study
title_full_unstemmed The association between TNP2 gene polymorphisms and Iranian infertile men with varicocele: A case-control study
title_short The association between TNP2 gene polymorphisms and Iranian infertile men with varicocele: A case-control study
title_sort association between tnp2 gene polymorphisms and iranian infertile men with varicocele: a case-control study
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6745086/
https://www.ncbi.nlm.nih.gov/pubmed/31583373
http://dx.doi.org/10.18502/ijrm.v17i8.4821
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