Stévant Isabelle, Abberbock Elisheva, Ridnik Meshi, Weiss Roni, Swisa Linoy, Futtner Christopher R, Maatouk Danielle M, Lovell-Badge Robin, Malysheva Valeriya, Gonen Nitzan
The Mina and Everard Goodman Faculty of Life Sciences and the Institute of Nanotechnology and Advanced Materials, Bar-Ilan University, Ramat Gan 5290002, Israel.
Department of Endocrinology, Northwestern University, Chicago, IL 60611, USA.
Sci Adv. 2025 Jul 25;11(30):eadv1885. doi: 10.1126/sciadv.adv1885.
Gonadal sex determination relies on tipping a delicate balance involving the activation and repression of several transcription factors and signaling pathways. This is likely mediated by numerous noncoding regulatory elements that shape sex-specific transcriptomic programs. To explore the dynamics of these in detail, we performed paired time series of transcriptomic and chromatin accessibility assays on pre-granulosa and Sertoli cells throughout their development in the embryo, making use of new and existing mouse reporter lines. Regulatory elements were associated with their putative target genes by linkage analysis, and this was complemented and verified experimentally using promoter capture Hi-C. We identified the transcription factor motifs enriched in these regulatory elements along with their occupancy, pinpointing LHX9/EMX2 as potentially critical regulators of ovarian development. Variations in the DNA sequence of these regulatory elements are likely to be responsible for many of the unexplained cases of individuals with differences of sex development.
性腺性别决定依赖于打破一种微妙的平衡,这种平衡涉及多种转录因子和信号通路的激活与抑制。这可能是由众多非编码调控元件介导的,这些元件塑造了性别特异性转录组程序。为了详细探究这些动态变化,我们利用新的和现有的小鼠报告基因系,在胚胎发育过程中对前颗粒细胞和支持细胞进行了配对的转录组和染色质可及性分析的时间序列实验。通过连锁分析将调控元件与其假定的靶基因关联起来,并使用启动子捕获Hi-C进行实验补充和验证。我们确定了这些调控元件中富集的转录因子基序及其占据情况,确定LHX9/EMX2为卵巢发育的潜在关键调节因子。这些调控元件DNA序列的变异可能是许多无法解释的性发育差异个体病例的原因。