Cnossen Wybrich R, te Morsche René H M, Hoischen Alexander, Gilissen Christian, Venselaar Hanka, Mehdi Soufi, Bergmann Carsten, Losekoot Monique, Breuning Martijn H, Peters Dorien J M, Veltman Joris A, Drenth Joost P H
Department of Gastroenterology and Hepatology, Institute for Genetic & Metabolic Disease (IGMD), Radboud Institute for Molecular LifeSciences (RIMLS), Radboud university medical center, Nijmegen, The Netherlands.
Department of Human Genetics, Institute for Genetic & Metabolic Disease (IGMD), Radboud Institute for Molecular LifeSciences (RIMLS), Radboud university medical center, Nijmegen, The Netherlands.
Eur J Hum Genet. 2016 Feb;24(2):237-42. doi: 10.1038/ejhg.2015.86. Epub 2015 Apr 29.
Mutations in Polycystic Kidney Disease proteins (PKD1 or PKD2) are causative for autosomal dominant polycystic kidney disease (ADPKD). However, a small subset of ADPKD probands do not harbor a mutation in any of the known genes. Low density lipoprotein Receptor-related Protein 5 (LRP5) was recently associated with hepatic cystogenesis in isolated polycystic liver disease (PCLD). Here, we demonstrate that this gene may also have a role in unlinked and sporadic ADPKD patients. In a cohort of 79 unrelated patients with adult-onset ADPKD, we identified a total of four different LRP5 variants that were predicted to be pathogenic by in silico tools. One ADPKD patient has a positive family history for ADPKD and variant LRP5 c.1680G>T; p.(Trp560Cys) segregated with the disease. Although also two PKD1 variants probably affecting protein function were identified, luciferase activity assays presented for three LRP5 variants significant decreased signal activation of canonical Wnt signaling. This study contributes to the genetic spectrum of ADPKD. Introduction of the canonical Wnt signaling pathway provides new avenues for the study of the pathophysiology.
多囊肾病蛋白(PKD1或PKD2)的突变是常染色体显性多囊肾病(ADPKD)的病因。然而,一小部分ADPKD先证者在任何已知基因中都没有突变。低密度脂蛋白受体相关蛋白5(LRP5)最近被发现与孤立性多囊肝病(PCLD)中的肝囊肿形成有关。在此,我们证明该基因在散发性ADPKD患者中可能也起作用。在一组79例成年发病的非相关ADPKD患者中,我们共鉴定出四种不同的LRP5变异体,计算机模拟工具预测它们具有致病性。一名ADPKD患者有ADPKD家族史,变异体LRP5 c.1680G>T;p.(Trp560Cys)与疾病共分离。虽然还鉴定出两个可能影响蛋白功能的PKD1变异体,但针对三个LRP5变异体的荧光素酶活性测定显示,经典Wnt信号的信号激活显著降低。本研究丰富了ADPKD的遗传谱。经典Wnt信号通路的引入为病理生理学研究提供了新途径。