Department of Animal and Food Sciences, Oklahoma State University, Stillwater, OK.
J Anim Sci. 2020 Jul 1;98(7). doi: 10.1093/jas/skaa205.
Ubiquitin-like with plant homeodomain and really interesting new gene finger domains 1 (UHRF1) is a multi-domain nuclear protein that plays an important role in epigenetics and tumorigenesis, but its role in normal ovarian follicle development remains unknown. Thus, the present study evaluated if UHRF1 mRNA abundance in bovine follicular cells is developmentally and hormonally regulated, and if changes in UHRF1 are associated with changes in DNA methylation in follicular cells. Abundance of UHRF1 mRNA was greater in granulosa cells (GC) and theca cells (TC) from small (<6 mm) than large (≥8 mm) follicles and was greater in small-follicle GC than TC. In GC and TC, fibroblast growth factor 9 (FGF9) treatment increased (P < 0.05) UHRF1 expression by 2-fold. Also, luteinizing hormone (LH) and insulin-like growth factor 1 (IGF1) increased (P < 0.05) UHRF1 expression in TC by 2-fold, and forskolin (an adenylate cyclase inducer) alone or combined with IGF1 increased (P < 0.05) UHRF1 expression by 3-fold. An E2F transcription factor inhibitor (E2Fi) decreased (P < 0.05) UHRF1 expression by 44% in TC and by 99% in GC. Estradiol, progesterone, and dibutyryl-cAMP decreased (P < 0.05) UHRF1 mRNA abundance in GC. Treatment of GC with follicle-stimulating hormone (FSH) alone had no effect but when combined with IGF1 enhanced the UHRF1 mRNA abundance by 2.7-fold. Beauvericin (a mycotoxin) completely inhibited the FSH plus IGF1-induced UHRF1 expression in small-follicle GC. Treatments that increased UHRF1 mRNA (i.e., FGF9) in GC tended to decrease (by 63%; P < 0.10) global DNA methylation, and those that decreased UHRF1 mRNA (i.e., E2Fi) in GC tended to increase (by 2.4-fold; P < 0.10) global DNA methylation. Collectively, these results suggest that UHRF1 expression in both GC and TC is developmentally and hormonally regulated, and that UHRF1 may play a role in follicular growth and development as well as be involved in ovarian epigenetic processes.
类泛素化蛋白与植物同源结构域和真核起始因子 1(UHRF1)是一种具有多种结构域的核蛋白,在表观遗传学和肿瘤发生中发挥重要作用,但它在正常卵巢卵泡发育中的作用尚不清楚。因此,本研究评估了牛卵泡细胞中 UHRF1mRNA 丰度是否受发育和激素调节,以及 UHRF1 的变化是否与卵泡细胞中 DNA 甲基化的变化相关。UHRF1mRNA 在小(<6mm)卵泡而非大(≥8mm)卵泡的颗粒细胞(GC)和膜细胞(TC)中丰度较高,且小卵泡 GC 中的丰度高于 TC。在 GC 和 TC 中,成纤维细胞生长因子 9(FGF9)处理使 UHRF1 表达增加了 2 倍(P<0.05)。此外,黄体生成素(LH)和胰岛素样生长因子 1(IGF1)使 TC 中的 UHRF1 表达增加了 2 倍(P<0.05),而单独使用福司可林(一种腺苷酸环化酶诱导剂)或与 IGF1 联合使用可使 UHRF1 表达增加 3 倍(P<0.05)。E2F 转录因子抑制剂(E2Fi)使 TC 中的 UHRF1 表达减少了 44%(P<0.05),GC 中的表达减少了 99%(P<0.05)。雌二醇、孕酮和二丁酰环腺苷酸(dibutyryl-cAMP)使 GC 中的 UHRF1mRNA 丰度降低(P<0.05)。单独用卵泡刺激素(FSH)处理 GC 没有影响,但与 IGF1 联合使用时可使 UHRF1mRNA 丰度增加 2.7 倍。白僵菌素(一种霉菌毒素)完全抑制了小卵泡 GC 中 FSH 加 IGF1 诱导的 UHRF1 表达。增加 GC 中 UHRF1mRNA(即 FGF9)的处理方法往往会降低(降低 63%;P<0.10)总体 DNA 甲基化,而降低 GC 中 UHRF1mRNA(即 E2Fi)的处理方法往往会增加(增加 2.4 倍;P<0.10)总体 DNA 甲基化。总的来说,这些结果表明,GC 和 TC 中的 UHRF1 表达受发育和激素调节,UHRF1 可能在卵泡生长和发育中发挥作用,并参与卵巢表观遗传过程。