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Publication : Oocyte-Derived Factors (GDF9 and BMP15) and FSH Regulate AMH Expression Via Modulation of H3K27AC in Granulosa Cells.

First Author  Roy S Year  2018
Journal  Endocrinology Volume  159
Issue  9 Pages  3433-3445
PubMed ID  30060157 Mgi Jnum  J:265699
Mgi Id  MGI:6200570 Doi  10.1210/en.2018-00609
Citation  Roy S, et al. (2018) Oocyte-Derived Factors (GDF9 and BMP15) and FSH Regulate AMH Expression Via Modulation of H3K27AC in Granulosa Cells. Endocrinology 159(9):3433-3445
abstractText  Anti-Mullerian hormone (AMH) produced by ovarian granulosa cells (GCs) plays a crucial role in ovarian function. It is used as a diagnostic and/or prognostic marker of fertility as well as for pathophysiological conditions in women. In this study, we investigated the underlying mechanism for regulation of AMH expression in GCs using primary mouse GCs and a human GC tumor-derived KGN cell line. We find that growth differentiation factor 9 (GDF9) and bone morphogenetic factor 15 (BMP15) together (GDF9 + BMP15), but not when tested separately, significantly induce AMH expression in vitro and in vivo (serum AMH). Our results show that GDF9 + BMP15 through the PI3K/Akt and Smad2/3 pathways synergistically recruit the coactivator p300 on the AMH promoter region that promotes acetylation of histone 3 lysine 27 (H3K27ac), facilitating AMH/Amh expression. Intriguingly, we also find that FSH inhibits GDF9 + BMP15-induced increase of AMH/Amh expression. This inhibition occurs through FSH-induced protein kinase A/SF1-mediated expression of gonadotropin inducible ovarian transcription factor 1, a transcriptional repressor, that recruits histone deacetylase 2 to deacetylate H3K27ac, resulting in the suppression of AMH/Amh expression. Furthermore, we report that ovarian Amh mRNA levels are significantly higher in Fshbeta-null mice (Fshbeta-/-) compared with those in wild-type (WT) mice. In addition, ovarian Amh mRNA levels are restored in Fshbeta-null mice expressing a human WT FSHbeta transgene (FSHbeta-/-hFSHbetaWT). Our study provides a mechanistic insight into the regulation of AMH expression that has many implications in female reproduction/fertility.
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