Bohaczuk Stephanie C, Tonsfeldt Karen J, Slaiwa Theresa I, Dunn Geneva A, Gillette Dominique L M, Yeo Seung E, Shi Chengxian, Cassin Jessica, Thackray Varykina G, Mellon Pamela L
Department of Obstetrics, Gynecology, and Reproductive Sciences, Center for Reproductive Science and Medicine, University of California, San Diego, La Jolla, CA 92093, USA.
Endocrinology. 2025 Apr 22;166(6). doi: 10.1210/endocr/bqaf073.
Follicle-stimulating hormone (FSH) is necessary for fertility in both sexes as a regulator of gametogenesis and hormone synthesis. Humans with loss-of-function mutations within the gene encoding the FSH beta subunit (FSHB) are infertile. Similarly, female Fshb knock-out mice are infertile and fail to ovulate, and males are subfertile. We recently reported the discovery and characterization of an upstream enhancer of FSHB located 26 Kb upstream of the transcriptional start site in humans (-17 Kb in mouse) that also amplifies activin and gonadotropin-releasing hormone induction of FSHB. Notably, the upstream enhancer contains a polymorphic, fertility-associated site in humans, rs11031006 (G/A), and the minor allele (A) increased enhancer activity in vitro as compared to the major allele (G), likely by increasing the affinity of an SF1 binding element. To investigate the role of the novel enhancer and rs11031006 variant in vivo, we created mouse models to assess deletion of the upstream enhancer and the impact of the G>A point mutation at the rs11031006-equivalent base. A full characterization of the -17 Kb enhancer deletion model revealed no apparent differences in fertility or serum FSH/LH levels, nor did a larger deletion that also included an additional putative regulatory element. In contrast, female mice homozygous for the mutated A allele at the rs11031006-equivalent position had fewer litters over a 120-day fertility assay, abnormal estrous cycling at 10 months, and reduced pituitary Lhb transcript abundance. Overall, while the mouse -17 Kb Fshb enhancer is dispensable for fertility, the rs11031006-equivalent G>A mutation results in subfertility in females.
促卵泡生成素(FSH)作为配子发生和激素合成的调节因子,对两性生育能力均至关重要。编码FSHβ亚基(FSHB)的基因发生功能丧失性突变的人类无法生育。同样,雌性Fshb基因敲除小鼠不育且不排卵,雄性则生育力低下。我们最近报告了在人类转录起始位点上游26 Kb处(小鼠为-17 Kb)发现并鉴定了FSHB的上游增强子,该增强子还能增强激活素和促性腺激素释放激素对FSHB的诱导作用。值得注意的是,该上游增强子在人类中包含一个与生育相关的多态性位点rs11031006(G/A),与主要等位基因(G)相比,次要等位基因(A)在体外增强了增强子活性,这可能是通过增加SF1结合元件的亲和力实现的。为了研究新型增强子和rs11031006变体在体内的作用,我们构建了小鼠模型,以评估上游增强子缺失以及rs11031006等效碱基处G>A点突变的影响。对-17 Kb增强子缺失模型的全面表征显示,生育能力或血清FSH/LH水平没有明显差异,包含另一个假定调控元件的更大缺失也未显示出差异。相比之下,在rs11031006等效位置纯合突变A等位基因的雌性小鼠在120天的生育试验中产仔数减少,10个月时发情周期异常,垂体Lhb转录本丰度降低。总体而言,虽然小鼠-17 Kb Fshb增强子对生育能力并非必需,但rs11031006等效的G>A突变导致雌性生育力低下。