Abundance of selected genes implicated in testicular Functions in Camelus dromedarius with high and low epididymal semen quality

• Published in: Biology of reproduction Vol. 110; no. 3; pp. 501 - 508
• Main Authors: Rashad, Dina E. M., Ibrahim, Sally, El-Sokary, Mohamed M. M., Mahmoud, Karima Gh. M., Abou El-Roos, Mahmoud E. A., Sosa, Gamal A. M., Kandiel, Mohamed M. M.
• Format: Journal Article
• Language: English
• Published: United States Society for the Study of Reproduction 13-03-2024; Oxford University Press
• Subjects: Biometrics; Breeding seasons; Camelidae; Camelids; DNA-directed RNA polymerase; dromedary camel; epididymal semen; Epididymis; ESR1 protein; Fertility; Gene expression; Gene regulation; Genes; Interleukin 6; Polymerase chain reaction; RESEARCH ARTICLE; Reverse transcription; Semen; Sperm; Testes; testis; Testosterone; dromedary camel; epididymal semen; testis; testosterone; gene expression
• ISSN: 0006-3363; 1529-7268
• DOI: 10.1093/biolre/ioad177

Studying testicular genes' expression may give key insights into precise regulation of its functions that influence epididymal sperm quality. The current study aimed to investigate the abundance of candidate genes involved in the regulation of testicular functions specially those regulate sperm function (PLA2G4D, SPP1, and CLUAP1), testicular steroidogenic function (ESR1 and AR), materials transport (AQP12B and LCN15), and defense mechanisms (DEFB110, GPX5, SOCS3, and IL6). Therefore, blood samples and testes with epididymis were collected from mature middle-aged (5–10 years) dromedary camels (n = 45) directly prior and after their slaughtering, respectively, during breeding season. Sera were evaluated for testosterone level and testicular biometry was measured with caliper. The epididymal tail semen was evaluated manually. Samples were distinguished based on testosterone level, testicular biometry, as well as epididymal semen features into high and low fertile groups. Total RNA was isolated from testicular tissues and gene expression was done using Quantitative Reverse Transcription Polymerase Chain Reaction (qRT-PCR). Results revealed that testosterone levels were significantly (P< 0.005) higher in camels with good semen quality than those of low quality. There was a significant (P< 0.0001) increase in testicular weight, length, width, thickness, and volume in high fertile than low fertile camels. PLA2G4D, SPP1, CLUAP1, ESR1, AR, AQP12B, LCN15, DEFB110, GPX5, and SOCS3 genes were upregulated (P< 0.001), and IL6 gene was downregulated (P< 0.01) in the testes of high fertile camels compared to the low fertile one. Thus, it could be concluded that examined genes might be valuable monitors of testicular functional status and fertility in dromedary camels. Graphical Abstract