Transgenerational effects induced by thiacloprid in Anterior prostate tissue are associated with alterations in DNA methylation at developmental genes
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Background
Neonicotinoids are widely used pesticides that cause a catastrophic decrease in bee and bumblebee populations worldwide. In addition to insects, neonicotinoids have toxic effects on other species, including lizards, birds, and mammals. Previous studies have shown that gestational exposure to thiacloprid has transgenerational effects on the testis and thyroids.
Objectives
In this project, we described the epigenetic effects of thiacloprid on anterior prostate tissue in directly exposed F1 males and nondirectly exposed F3 males
Methods
We used paraffin sections for morphological analysis, frozen tissue sections for immunofluorescence analysis, RT‒qPCR for gene expression analysis, histone purification and western blotting for protein analysis, and ChIP‒qPCR for histone H3K4me3 occupancy analysis.
The results
We observed a tendency toward an increase in epithelial hyperplasia in F1 and not a significant increase in F3. We detected elevated levels of phosphorylated histone H3 at serine 10, a marker of mitosis, in both the F1 and F3 prostates. A significant increase in the level of the Ki-67 marker of proliferation was detected in the F1 anterior prostate but not in the F3 anterior prostate. Hox gene expression was upregulated in F1 anterior prostate and downregulated in F3 anterior prostate. The changes in gene expression were associated with histone H3K4me3 alterations at the promoters of the genes. We determined that regions of Hox genes that play important roles in the anterior prostate have altered DNA methylation in the sperm of F1 and F3. These alterations in DNA methylation were negatively related to gene expression.
Conclusion
Our analysis revealed that gestational exposure to thiacloprid caused epigenetic alterations in the anterior prostates of F1 males and nondirectly exposed F3 males. DNA methylation changes at the promoters of anterior prostate development genes could be responsible for transgenerational effects in anterior prostates.
