LaVoie Holly A
Department of Cell and Developmental Biology and Anatomy, University of South Carolina School of Medicine, Columbia, SC 29208, USA.
Mol Cell Endocrinol. 2005 Nov 24;243(1-2):12-8. doi: 10.1016/j.mce.2005.09.005. Epub 2005 Oct 10.
The dynamic nature of the ovarian follicle makes it an ideal model to study the coordinated activation and inactivation of genes related to cell growth and differentiation. Much progress has been made in identifying transcription factors that promote the transcription of ovarian genes mediating gonadotropin action and steroidogenesis, but how these factors promote transcription in the context of chromatin is not well understood. Over the past 5 years, epigenetic regulation of ovarian genes through histone modifications has been the focus of an increasing number of studies. Several coactivators and corepressors associated with transcription factors are in fact histone acetyltransferases and histone deacetylases mediating the hyperacetylation and hypoacetylation of histones, respectively. Hyperacetylation of lysine residues in the core histone tails promotes chromatin alterations that favor transcription, whereas hypoacetylation of histones promotes gene silencing or repression. Not only does the acetylation status of the core histones determine whether chromatin remodeling occurs, but histone phosphorylation and methylation may serve equally important roles. For example, the combination of histone H3 phosphorylation and acetylation concertedly favors transcription. In addition, specific lysine methylations (e.g., K9 of histone H3) repress gene expression whereas other methylations promote gene expression. It is most likely the combination of histone modification events that regulate the initiation of transcription. Understanding how ovarian hormones control specific histone modifications will help us understand how follicular cells can switch from active gene pools governing cell proliferation to those gene groups controlling terminal differentiation. Progress in elucidating the ovarian specific regulation of histone modifying enzymes as well as identification of their target gene pools at different stages of the follicular cycle is expected in the next few years.
卵巢卵泡的动态特性使其成为研究与细胞生长和分化相关基因的协同激活和失活的理想模型。在识别促进介导促性腺激素作用和类固醇生成的卵巢基因转录的转录因子方面已经取得了很大进展,但这些因子如何在染色质环境中促进转录尚不清楚。在过去5年中,通过组蛋白修饰对卵巢基因进行表观遗传调控已成为越来越多研究的焦点。实际上,与转录因子相关的几种共激活因子和共抑制因子分别是介导组蛋白高乙酰化和低乙酰化的组蛋白乙酰转移酶和组蛋白去乙酰化酶。核心组蛋白尾巴中赖氨酸残基的高乙酰化促进有利于转录的染色质改变,而组蛋白的低乙酰化促进基因沉默或抑制。不仅核心组蛋白的乙酰化状态决定染色质重塑是否发生,组蛋白磷酸化和甲基化可能也起着同样重要的作用。例如,组蛋白H3磷酸化和乙酰化的组合协同促进转录。此外,特定的赖氨酸甲基化(例如组蛋白H3的K9)抑制基因表达,而其他甲基化促进基因表达。很可能是组蛋白修饰事件的组合调节转录的起始。了解卵巢激素如何控制特定的组蛋白修饰将有助于我们理解卵泡细胞如何从控制细胞增殖的活跃基因库转变为控制终末分化的基因组。预计在未来几年内,在阐明组蛋白修饰酶的卵巢特异性调控以及在卵泡周期不同阶段鉴定其靶基因库方面将取得进展。