Transcriptomic analysis reveals gene expression changes due to prenatal NeuroMix exposure in males and females, suggesting sex-specific effects on the HPG axis.
Endocrine-disrupting chemicals (EDCs) are exogenous chemicals ubiquitous in our environment and found in everyday items. We previously reported that prenatal exposure of rats to a human-relevant mixture of EDCs, “NeuroMix,” led to alterations in physiological and behavioral phenotypes. Here, we used hypothalamic-pituitary-gonadal (HPG) tissues from these same male and female rats and conducted 3’ Tag-based RNA sequencing (TagSeq) to investigate underlying molecular mechanisms. TagSeq revealed unique tissue- and sex-specific differentially expressed genes. In males, among the HPG tissues, NMX had the greatest effects in the hypothalamic arcuate nucleus (ARC), with 613 differentially expressed genes (DEGs). GO-enrichment analysis revealed genes up-regulated in the ARC of NMX males were involved in synaptic plasticity, while genes down-regulated related to responses to estradiol and glucocorticoids. In females, prenatal NMX exposure induced the largest transcriptome change in the ovaries, with 1295 DEGs. GO-enrichment analysis revealed up-regulation of genes involved in cilium organization and movement, while genes down-regulated in this region were related to immune-related processes. Using Qiagen Ingenuity Pathway Analysis, we identified the beta-estradiol pathway to be activated in all NMX female tissues and NMX male pituitary, and inhibited in NMX male, ARC, VMN, and testes. To our knowledge this is one of the first studies to conduct transcriptomic profiling across HPG tissues, with these results demonstrating that prenatal exposure to NMX affects gene expression across the HPG axis in a sex-dependent matter.
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Milewski et al. (2025) studied this question.
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