Male infertility and copy number variants (CNVs) in the dog: a two-pronged approach using Computer Assisted Sperm Analysis (CASA) and Fluorescent In Situ Hybridization (FISH).
Articolo
Data di Pubblicazione:
2013
Abstract:
Background
Infertility affects ~10-15% of couples trying to have children, in which the rate of male
fertility problems is approximately at 30-50%. Copy number variations (CNVs) are DNA
sequences greater than or equal to 1 kb in length sharing a high level of similarity and present
at a variable number of copies in the genome; in our study, we used the canine species as an
animal model to detect CNVs responsible for male infertility. We aim to identify CNVs
associated with male infertility in the dog genome with a two-pronged approach: we
performed a sperm analysis using the CASA system and a cytogenetic-targeted analysis on
genes involved in male gonad development and spermatogenesis with fluorescence in situ
hybridization (FISH), using dog-specific clones. This analysis was carried out to evaluate
possible correlations between CNVs on targeted genes and spermatogenesis impairments or
infertility factors.
Results
We identified two genomic regions hybridized by BACs CH82-321 J09 and CH82-509B23
showing duplication patterns in all samples except for an azoospermic dog. These two
regions harbor two important genes for spermatogenesis: DNM2 and TEKT1. The genomic
region encompassed by the BAC clone CH82-324I01 showed a single-copy pattern in all
samples except for one dog, assessed with low-quality sperm, displaying a marked
duplication pattern. This genomic region harbors SOX8, a key gene for testis development.
Conclusion
We present the first study involving functional and genetic analyses in male infertility. We
set up an extremely reliable analysis on dog sperm cells with a highly consistent statistical
significance, and we succeeded in conducting FISH experiments on sperm cells using BAC
clones as probes. We found copy number differences in infertile compared with fertile dogs
for genomic regions encompassing TEKT1, DNM2, and SOX8, suggesting they could have a
role in fertility if deleted or duplicated with respect to the reference copy number in fertility
biology. This method is of particular interest in the canine species due to the recognized role
of this species as an animal model for the study of human genetic diseases and could be
useful for other species of economic interest and for endangered animal species.
Tipologia CRIS:
01.01 Articolo in rivista
Elenco autori:
Pizzi, Flavia
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