Institute for Molecular Bioscience, The University of Queensland, St. Lucia 4072, Australia.
Dev Biol. 2010 Aug 15;344(2):1071-87. doi: 10.1016/j.ydbio.2010.05.495. Epub 2010 May 24.
Here we describe the first detailed catalog of gene expression in the developing lower urinary tract (LUT), including epithelial and mesenchymal portions of the developing bladder, urogenital sinus, urethra, and genital tubercle (GT) at E13 and E14. Top compartment-specific genes implicated by the microarray data were validated using whole-mount in situ hybridization (ISH) over the entire LUT. To demonstrate the potential of this resource to implicate developmentally critical features, we focused on gene expression patterns and pathways in the sexually indeterminate, androgen-independent GT. GT expression patterns reinforced the proposed similarities between development of GT, limb, and craniofacial prominences. Comparison of spatial expression patterns predicted a network of Wnt7a-associated GT-enriched epithelial genes, including Gjb2, Dsc3, Krt5, and Sostdc1. Known from other contexts, these genes are associated with normal epidermal differentiation, with disruptions in Dsc3 and Gjb2 showing palmo-plantar keratoderma in the limb. We propose that this gene network contributes to normal foreskin, scrotum, and labial development. As several of these genes are known to be regulated by, or contain cis elements responsive to retinoic acid, estrogen, or androgen, this implicates this pathway in the later androgen-dependent development of the GT.
在这里,我们描述了第一个详细的下尿路(LUT)发育过程中的基因表达目录,包括膀胱、尿生殖窦、尿道和生殖嵴(GT)的上皮和间充质部分,在 E13 和 E14 时进行了研究。通过微阵列数据鉴定的顶级隔室特异性基因,使用整个 LUT 的全胚胎原位杂交(ISH)进行了验证。为了证明该资源有潜力涉及发育关键特征,我们专注于性未分化、雄激素非依赖性 GT 中的基因表达模式和途径。GT 的表达模式强化了 GT、肢体和颅面突起发育之间相似性的假设。空间表达模式的比较预测了一个与 Wnt7a 相关的 GT 上皮基因网络,包括 Gjb2、Dsc3、Krt5 和 Sostdc1。从其他背景中已知,这些基因与正常表皮分化有关,Dsc3 和 Gjb2 的破坏在肢体中导致掌跖角化病。我们提出,这个基因网络有助于正常的包皮、阴囊和阴唇发育。由于这些基因中的几个已知受到视黄酸、雌激素或雄激素的调节,或者包含对其有反应的顺式元件,这表明该途径参与了 GT 的后期雄激素依赖性发育。