Journal
MOLECULAR REPRODUCTION AND DEVELOPMENT
Volume 88, Issue 3, Pages 238-248Publisher
WILEY
DOI: 10.1002/mrd.23463
Keywords
CL; methoxychlor; miRNA; pig; RNA‐ Seq
Funding
- National Science Centre, Poland
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This study investigated the impact of neonatal exposure to MXC on luteal function in pigs, showing changes in luteal steroid and prostaglandin concentrations. The results also indicated differential expression of miRNAs and genes related to various physiological processes in the luteal tissue. Negative correlation analysis suggested potential interactions between miRNAs and specific messenger RNAs, potentially mediating the long-term effects of MXC on CL function in pigs.
This study investigated the effects of neonatal exposure to methoxychlor (MXC), a synthetic organochlorine used as an insecticide with estrogenic, antiestrogenic, and antiandrogenic activities, on luteal function in pigs. Piglets were injected subcutaneously with MXC (20 mu g/kg body weight) or corn oil (control) between postnatal Days 1 and 10 (N = 5/group). Corpora lutea from sexually mature gilts were examined for luteal steroid and prostaglandin concentrations and processed for total RNA isolation and subsequent RNA sequencing. Intra-luteal concentrations of androstenedione and prostaglandin E-2 were greater, while that of estrone was lower when compared to control. Fifty-three differentially expressed (DE) microRNAS (miRNAs) (p-adjusted <.05 and log2(fold change) >=.5) and 359 DE genes (p-adjusted <.05 and log2(fold change) >= 1) were identified in luteal tissue in response to neonatal MXC treatment. MXC was found to affect the expression of genes related to lipogenesis, steroidogenesis, membrane transport, immune response, cell signaling and adhesion. These results suggest an earlier onset of structural luteolysis in pigs caused by MXC actions in neonates. Since negative correlation analysis showed the potential interactions of miRNAs with specific messenger RNAs, we propose that these miRNAs are potential mediators of the long-term MXC effect on the CL function in pigs.
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