Garcia-Moreno S Alexandra, Futtner Christopher R, Salamone Isabella M, Gonen Nitzan, Lovell-Badge Robin, Maatouk Danielle M
Department of Obstetrics and Gynecology, Northwestern University, Chicago, IL 60611, United States.
Department of Endocrinology, Northwestern University, Chicago, IL 60611, United States.
Dev Biol. 2019 Feb 15;446(2):168-179. doi: 10.1016/j.ydbio.2018.12.023. Epub 2018 Dec 27.
Cis-regulatory elements are critical for the precise spatiotemporal regulation of genes during development. However, identifying functional regulatory sites that drive cell differentiation in vivo has been complicated by the high numbers of cells required for whole-genome epigenetic assays. Here, we identified putative regulatory elements during sex determination by performing ATAC-seq and ChIP-seq for H3K27ac in purified XX and XY gonadal supporting cells before and after sex determination in mice. We show that XX and XY supporting cells initiate sex determination with similar chromatin landscapes and acquire sex-specific regulatory elements as they commit to the male or female fate. To validate our approach, we identified a functional gonad-specific enhancer downstream of Bmp2, an ovary-promoting gene. This work increases our understanding of the complex regulatory network underlying mammalian sex determination and provides a powerful resource for identifying non-coding regulatory elements that could harbor mutations that lead to Disorders of Sexual Development.
顺式调控元件对于发育过程中基因精确的时空调控至关重要。然而,由于全基因组表观遗传学检测需要大量细胞,因此在体内鉴定驱动细胞分化的功能性调控位点变得复杂。在这里,我们通过在小鼠性别决定前后对纯化的XX和XY性腺支持细胞进行H3K27ac的ATAC-seq和ChIP-seq,鉴定了性别决定过程中的假定调控元件。我们表明,XX和XY支持细胞在启动性别决定时具有相似的染色质景观,并在决定走向雄性或雌性命运时获得性别特异性调控元件。为了验证我们的方法,我们在促进卵巢发育的基因Bmp2下游鉴定了一个功能性的性腺特异性增强子。这项工作增进了我们对哺乳动物性别决定背后复杂调控网络的理解,并为鉴定可能携带导致性发育障碍突变的非编码调控元件提供了强大的资源。