Expression profiles of meiotic genes in male vs. female gonads and gametes: Insights into fertility issues

Front Genet. 2023 Mar 14:14:1125097. doi: 10.3389/fgene.2023.1125097. eCollection 2023.

Abstract

Gametes are specialized cells that, at fertilization, give rise to a totipotent zygote capable of generating an entire organism. Female and male germ cells undergo meiosis to produce mature gametes; however, sex-specific events of oogenesis and spermatogenesis contribute to specific roles of gametes in reproductive issues. We investigate the differential gene expression (DGE) of meiosis-related genes in human female and male gonads and gametes in normal and pathological conditions. The transcriptome data for the DGE analysis was obtained through the Gene Expression Omnibus repository, comprising human ovary and testicle samples of the prenatal period and adulthood, additionally to male (non-obstructive azoospermia (NOA) and teratozoospermia), and female (polycystic ovary syndrome (PCOS) and advanced maternal age) reproductive conditions. Gene ontology terms related to meiosis were associated with 678 genes, of which 17 genes in common were differentially expressed between the testicle and ovary during the prenatal period and adulthood. Except for SERPINA5 and SOX9, the 17 meiosis-related genes were downregulated in the testicle during the prenatal period and upregulated in adulthood compared to the ovary. No differences were observed in the oocytes of PCOS patients; however, meiosis-related genes were differentially expressed according to the patient's age and maturity of the oocyte. In NOA and teratozoospermia, 145 meiosis-related genes were differentially expressed in comparison to the control, including OOEP; despite no recognized role in male reproduction, OOEP was co-expressed with genes related to male fertility. Taking together, these results shed light on potential genes that might be relevant to comprehend human fertility disorders.

Keywords: germinal vesicle; infertility; mature oocyte; oogenesis; spermatogenesis.

Grants and funding

This work was supported by the Fundo de Incentivo à Pesquisa e Evento (FIPE) do Hospital de Clínicas de Porto Alegre (grants numbers 2019-0173 and 2019-0479), as well as Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES–grant number 88887.503016/2020-00).