The human epididymal protease inhibitor (Eppin) gene is specifically expressed in testis and epididymis and is important in male reproduction. However, to date, there is no report on variants of this gene, particularly in relation to male fertility. To investigate the association between Eppin genetic variants and semen quality, variant genotyping and semen analysis was performed in 473 males with definite idiopathic infertility by polymerase chain reaction-restriction fragment length polymorphism and computer-assisted semen analysis. It was found that rs6124715 GG/CG genotypes were associated with a significantly higher curvilinear velocity (VCL) (P=0.029 and 0.021 respectively) and average path velocity (VAP) (P=0.043 and 0.016 respectively) compared with the CC genotype. The straight line velocity (VSL) between rs6124715 CG and CC genotype was also significantly different (P=0.019). Regarding variant rs11594, subjects with C allele (CC or AC) had significantly lower VCL (P=0.011 and 0.046 respectively), VSL (P=0.025 and 0.041 respectively) and VAP (P=0.026 and 0.030 respectively) in comparison with AA homozygote. The sperm number per ejaculate was also significantly different between rs2231829 TT and CC genotype (P=0.042). These findings indicate, for the first time, that the genetic variants in the Eppin gene may be associated with semen quality.
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http://dx.doi.org/10.1016/j.rbmo.2009.10.025 | DOI Listing |
Proc Natl Acad Sci U S A
December 2024
Center for Drug Discovery, Department of Pathology & Immunology, Baylor College of Medicine, Houston, TX 77030.
Despite 96 million years of evolution separating humans and rodents, 11 closely related reproductive tract-specific genes in humans-, , , , , , , , , , and -and the 13 reproductive tract-specific orthologous genes in mice, form highly conserved syntenic gene clusters indicative of conserved, combined critical functions. Further, despite significant progress toward a nonhormonal male contraceptive targeting the protein encoded by one of these genes, epididymal peptidase inhibitor (EPPIN), and associations found between mutations in and an increased risk of male infertility, neither EPPIN nor any closely related whey acidic protein four-disulfide core (WFDC) gene have been explored functionally. To clarify the involvement of WFDC genes in male fertility, we strategically used CRISPR/Cas9 to generate mice lacking 13, 10, 5, or 4 genes within the cluster and demonstrated that males with deletions of 13, 10, or 4 genes (Wfdc6a, Eppin, Wfdc8, and Wfdc6a) were sterile due to an arrest in spermatogenesis, preventing formation beyond round spermatids.
View Article and Find Full Text PDFHum Reprod Update
September 2023
Department of Biophysics and Pharmacology, Institute of Biosciences of Botucatu, São Paulo State University, Botucatu, Brazil.
Front Oncol
November 2021
Department of Pathology, The Affiliated Hospital of Qingdao University, Qingdao, China.
Goblet cell adenocarcinoma (GCA) is a rare amphicrine tumor and difficult to diagnose. GCA is traditionally found in the appendix, but extra-appendiceal GCA may be underestimated. Intestinal adenocarcinoma with signet ring cell component is also very rare, and some signet ring cell carcinomas are well cohesive, having some similar morphological features to GCAs.
View Article and Find Full Text PDFReprod Biol
June 2021
Department of Toxicology, School of Public Health, Medical College of Soochow University, Suzhou, China; Jiangsu Key Laboratory of Preventive and Translational Medicine for Geriatric Diseases, School of Public Health, Medical College of Soochow University, Suzhou, China. Electronic address:
Epididymal protease inhibitor (EPPIN) is differentially expressed in the reproductive tissues (such as testicles, outlet tubes, epididymis, vas deferens, and seminal vesicles). Its critical role in sperm function and male reproduction has shed light on EPPIN as a candidate target for male contraceptive vaccines. In this study, we endeavored to further reveal the mechanism through which EPPIN exerts its function.
View Article and Find Full Text PDFFuture Oncol
December 2020
Department of Aeronautics & Astronautics, Fudan University, Shanghai, 200433, PR China.
To uncover the molecular mechanisms of early-onset ovarian serous cystadenocarcinoma (EOOSC; patients <50 years old) and late-onset ovarian serous cystadenocarcinoma (LOOSC; patients ≥50 years old). Bioinformatics was utilized to identify the key factors. 478 EOOSC and 899 LOOSC individual differentially expressed genes were identified and enriched in different pathways.
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