Institute for Anatomy and Cell Biology, University Hospital Bonn, University of Bonn, Bonn, Germany.
Institute for Neuroanatomy, University Hospital Bonn, University of Bonn, Bonn, Germany.
Commun Biol. 2022 Nov 9;5(1):1203. doi: 10.1038/s42003-022-04092-3.
Classic bladder exstrophy represents the most severe end of all human congenital anomalies of the kidney and urinary tract and is associated with bladder cancer susceptibility. Previous genetic studies identified one locus to be involved in classic bladder exstrophy, but were limited to a restrict number of cohort. Here we show the largest classic bladder exstrophy genome-wide association analysis to date where we identify eight genome-wide significant loci, seven of which are novel. In these regions reside ten coding and four non-coding genes. Among the coding genes is EFNA1, strongly expressed in mouse embryonic genital tubercle, urethra, and primitive bladder. Re-sequence of EFNA1 in the investigated classic bladder exstrophy cohort of our study displays an enrichment of rare protein altering variants. We show that all coding genes are expressed and/or significantly regulated in both mouse and human embryonic developmental bladder stages. Furthermore, nine of the coding genes residing in the regions of genome-wide significance are differentially expressed in bladder cancers. Our data suggest genetic drivers for classic bladder exstrophy, as well as a possible role for these drivers to relevant bladder cancer susceptibility.
经典膀胱外翻代表了人类所有肾脏和泌尿道先天异常中最严重的一种,与膀胱癌易感性相关。先前的遗传研究确定了一个与经典膀胱外翻相关的基因座,但这些研究仅限于少数队列。在这里,我们进行了迄今为止最大的经典膀胱外翻全基因组关联分析,鉴定出 8 个全基因组显著的基因座,其中 7 个是新的。这些区域包含 10 个编码基因和 4 个非编码基因。在这些编码基因中,EFNA1 在小鼠胚胎生殖结节、尿道和原始膀胱中强烈表达。我们对本研究中经典膀胱外翻队列中的 EFNA1 进行了重新测序,显示出罕见的蛋白质改变变异体的富集。我们表明,所有编码基因在小鼠和人类胚胎发育膀胱阶段都有表达和/或显著调控。此外,位于全基因组显著水平的 9 个编码基因在膀胱癌中差异表达。我们的数据表明了经典膀胱外翻的遗传驱动因素,以及这些驱动因素与膀胱癌易感性的可能关系。