Transgenerational inheritance of diminished ovarian reserve triggered by prenatal propylparaben exposure in mice

作者：Milu Li, Yaling Wu, Siting Wei, Tianyu Zhang, Wei Yan, Yueyue Gao, Yingying Chen, Dianxing Hu, Tong Wu, Mo Li, Wenwen Wang, Yan Li, Su Zhou, Ximiao He, Shixuan Wang, Jinjin Zhang · 发表于：Nature Communications · 年份：2025 · DOI：10.1038/s41467-025-63440-z · 被引用次数：4 · 研究领域：Mitochondrial Function and Pathology、Metabolism and Genetic Disorders、Anesthesia and Neurotoxicity Research

Diminished ovarian reserve (DOR) is associated with heightened risk of infertility, premature menopause, and various long-term health issues. Our previous research demonstrated a correlation between prenatal propylparaben exposure and DOR in F1 mice. Here, we further reveal that the DOR phenotypes can be transgenerationally inherited in F1-F3 mice, manifested through increased follicular atresia and decreased anti-Müllerian hormone levels. Excessive apoptosis of granulosa cells is found to underlie these pathological processes. By combining diverse sequencing techniques, we identify persistent Rhobtb1 hypomethylation across multiple generations. Further exploration reveals that RhoBTB1 regulates FGF18 via ubiquitination, triggering MAPK pathway activation and subsequent granulosa cell apoptosis. Notably, similar Rhobtb1 hypomethylation patterns are observed in blood samples from DOR patients. Furthermore, intervention with a methyl-donor diet effectively ameliorates DOR phenotypes in F1-F3 offspring. These findings highlight the transgenerational effects of DOR, elucidate its underlying causes and pathogenic mechanisms, and propose potential epigenetic therapy strategies. The authors show that prenatal propylparaben exposure causes transgenerational inheritance of diminished ovarian reserve via Rhobtb1 hypomethylation, with similar patterns in patient samples. Methyl-donor diet counteracts this, suggesting therapeutic potential.