Georges Adrien, Auguste Aurelie, Bessière Laurianne, Vanet Anne, Todeschini Anne-Laure, Veitia Reiner A
CNRS UMR 7592, Institut Jacques Monod, 15 Rue Hélène Brion, 75013 Paris, France Université Paris Diderot, Paris VII, Paris, France.
J Mol Endocrinol. 2013 Dec 19;52(1):R17-33. doi: 10.1530/JME-13-0159. Print 2014 Feb.
Forkhead box L2 (FOXL2) is a gene encoding a forkhead transcription factor preferentially expressed in the ovary, the eyelids and the pituitary gland. Its germline mutations are responsible for the blepharophimosis ptosis epicanthus inversus syndrome, which includes eyelid and mild craniofacial defects associated with primary ovarian insufficiency. Recent studies have shown the involvement of FOXL2 in virtually all stages of ovarian development and function, as well as in granulosa cell (GC)-related pathologies. A central role of FOXL2 is the lifetime maintenance of GC identity through the repression of testis-specific genes. Recently, a highly recurrent somatic FOXL2 mutation leading to the p.C134W subtitution has been linked to the development of GC tumours in the adult, which account for up to 5% of ovarian malignancies. In this review, we summarise data on FOXL2 modulators, targets, partners and post-translational modifications. Despite the progresses made thus far, a better understanding of the impact of FOXL2 mutations and of the molecular aspects of its function is required to rationalise its implication in various pathophysiological processes.
叉头框L2(FOXL2)是一个编码叉头转录因子的基因,该因子在卵巢、眼睑和垂体中优先表达。其种系突变导致睑裂狭小、上睑下垂、内眦赘皮综合征,该综合征包括与原发性卵巢功能不全相关的眼睑和轻度颅面缺陷。最近的研究表明,FOXL2几乎参与卵巢发育和功能的所有阶段,以及颗粒细胞(GC)相关的病理过程。FOXL2的核心作用是通过抑制睾丸特异性基因来维持GC身份的终生稳定性。最近,一种导致p.C134W替换的高度复发性体细胞FOXL2突变与成人GC肿瘤的发生有关,GC肿瘤占卵巢恶性肿瘤的比例高达5%。在这篇综述中,我们总结了关于FOXL2调节剂、靶点、相互作用蛋白和翻译后修饰的数据。尽管迄今为止已取得进展,但仍需要更好地了解FOXL2突变的影响及其功能的分子层面,以便合理地解释其在各种病理生理过程中的作用。