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Kernanec, P.-Y.

Publications and source records attributed to Kernanec, P.-Y..

2 recordsLinked to original sources

Transgenerational effects induced by thiacloprid in Anterior prostate tissue are associated with alterations in DNA methylation at developmental genes.

BackgroundNeonicotinoids 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. ObjectivesIn this project, we described the epigenetic effects of thiacloprid on anterior prostate tissue in directly exposed F1 males and nondirectly exposed F3 males MethodsWe 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 resultsWe 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. ConclusionOur 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.

developmental biology↗

EXOSC10/Rrp6 is essential for the eight-cell embryo/morula transition

The conserved 3-5 exoribonuclease EXOSC10/Rrp6 is required for gametogenesis, brain development, erythropoiesis and blood cell enhancer function. The human ortholog is essential for mitosis in cultured cancer cells. Little is known, however, about the role of Exosc10 during embryo development and organogenesis. We generated an Exosc10 knockout model and find that Exosc10-/- mice show an embryonic lethal phenotype. We demonstrate that Exosc10 maternal wild type mRNA is present in mutant oocytes and that the gene is expressed during all stages of early embryogenesis. Furthermore, we observe that EXOSC10 early on localizes to the periphery of nucleolus precursor bodies in blastomeres, which is in keeping with the proteins role in rRNA processing and may indicate a function in the establishment of chromatin domains during initial stages of embryogenesis. Finally, we infer from genotyping data for embryonic days e7.5, e6.5 and e4.5 and embryos cultured in vitro that Exosc10-/- mutants arrest at the eight-cell embryo/morula transition. Our results demonstrate a novel essential role for Exosc10 during early embryogenesis, and they are consistent with earlier work showing that impaired ribosome biogenesis causes a developmental arrest at the morula stage.

developmental biology↗