Author/Authors :
Heydarian، Neda نويسنده Royan Institute for Reproductive Biomedicine, Reproductive Biomedicine Research Center,Department of Genetics,Academic Center for Education, Culture and Research (ACECR),Tehran,Iran , , Favaedi، Raha نويسنده Reproductive Biomedicine Research Center, Royan Institute for Reproductive Biomedicine,Department of Genetics,Academic Center for Education, Culture and Research (ACECR),Iran , , Sadighi Gilani، Mohammad Ali نويسنده Reproductive Biomedicine Research Center, Royan Institute for Reproductive Biomedicine,Department of Andrology,Academic Center for Education, Culture and Research (ACECR),Tehran,Iran , , Shahhoseini، Maryam نويسنده Reproductive Biomedicine Research Center, Royan Institute for Reproductive Biomedicine,Department of Genetics,Academic Center for Education, Culture and Research (ACECR),Tehran,Iran ,
Abstract :
Background: The availability of testis specific genes will be of help in choosing the most promising biomarkers for the detection of testicular sperm retrieval in patients with non-obstructive azoospermia (NOA). Testis specific chromodomain protein Y 1 (CDY1) is a histone acetyltransferase which concentrates in the round spermatid nucleus, where histone hyperacetylation occurs and causes the replacement of histones by the sperm-specific DNA packaging proteins, TNPs and PRMs. Objective: The aim was to evaluate CDY1 gene as a marker for predicting of successful sperm retrieval in NOA patients. Materials and Methods: This research was conducted on 29 patients with NOA who had undergone testicular sperm extraction (TESE) procedure. NOA patients were subdivided into patients with successful sperm retrieval (NOA+, n=12) and patients with unsuccessful sperm retrieval (NOA-, n=17). Relative expression of CDY1 gene and chromatin incorporation of CDY1 protein were measured by quantitative real-time polymerase chain reaction (qRT-PCR) and ELISA assay, respectively.
Results: Quantification of mRNA relative expression and incorporation of CDY1 protein in chromatin showed significant lower expressions and protein levels of CDY1 in testis tissues of NOA- in comparison to NOA+ group. Conclusion: The findings in this study demonstrated a correlation between the low levels of CDY1 function and unsuccessful sperm recovery in the testicular tissues of NOA- compared to NOA+ patients. Therefore, it can be reasonable to consider CDY1 as a potential biomarker for predicting the presence of spermatozoa, although the claim needs more samples to be confirmed.
Keywords :
Azoospermia , CDY1 , Gene expression , Marker