Expression profiles of circular RNAs in spermatozoa from aging men

Author:

Zhou Qiao1,Liu Anming1,Ji Hui2,Ji Juan1,Sun Jingwen1,Ling Zhonghui1,Li Guangyao1,Ling Xiufeng1,Xu Lu1,Chen Xiaoning3ORCID

Affiliation:

1. Women's Hospital of Nanjing Medical University: Nanjing Maternity and Child Health Care Hospital

2. Women's College Hospital

3. Nanjing Medical University Affiliated Healthcare Hospital for Women and Infants: Nanjing Maternity and Child Health Care Hospital

Abstract

Abstract Background Advanced paternal age (APA) is associated with decreased fertility, but the mechanism underlying APA remains unknown. CircRNAs have been reported to be ideal candidate biomarkers for diagnostic and therapeutic applications in many diseases and are also involved in spermatogenesis. Hence, we aimed to assess the circRNA expression profile of spermatozoa from aging men. Methods and Results We recruited 6 subjects, including 3 in the younger group (men age < 40) and 3 in the APA group (men age≥40). RNA sequencing was exploited to identify the expression profiles of circRNAs between the two groups. The expression levelsof circRNAs were validated using real-time quantitative polymerase chain reaction (RT–qPCR). Kyoto Encyclopedia of Genes and Genomes biological pathway analysis and Gene Ontologyanalysis were performed to evaluate the functions of differentially expressed circRNAs (DE-circRNAs) between the two groups. In total, 18,787 circRNAs were sequenced in the spermatozoa of two groups. Our analysis revealed that there were 1056 downregulated circRNAs and 1228 upregulated circRNAs between the two groups, and KEGG analysis showed they were mainly involved in pathways including the DNA repair signaling pathway, meiotic recombination signaling pathway, and PI3K/AKT signaling pathway. Conclusions In conclusion, our study suggested that circRNAs play a vital role in spermatozoa from aging men and provided a fresh perspective on the specific regulatory mechanism of spermatozoa from aging men.

Publisher

Research Square Platform LLC

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