Department of Nephrology, National Center for Child Health and Development, Tokyo, Japan.
Pediatr Nephrol. 2010 Jun;25(6):1073-9. doi: 10.1007/s00467-010-1454-9. Epub 2010 Feb 13.
Hepatocyte nuclear factor 1beta (HNF1beta) abnormalities have been recognized to cause congenital anomalies of the kidney and urinary tract (CAKUT), predominantly affecting bilateral renal malformations. To further understand the spectrum of HNF1beta related phenotypes, we performed HNF1B gene mutation and deletion analyses in Japanese patients with renal hypodysplasia (n = 31), unilateral multicystic dysplastic kidney (MCDK; n = 14) and others (n = 5). We identified HNF1B alterations in 5 out of 50 patients (10%). De novo heterozygous complete deletions of HNF1B were found in 3 patients with unilateral MCDK. Two of the patients showed contralateral hypodysplasia, whereas the other patient showed a radiologically normal contralateral kidney with normal renal function. Copy number variation analyses showed 1.4 Mb microdeletions involving the whole HNF1B gene with breakpoints in flanking segmental duplications. We also identified 1 novel truncated mutation (1007insC) and another missense mutation (226G>T) in patients with bilateral hypodysplasia. HNF1B alterations leading to haploinsufficiency affect a diverse spectrum of CAKUT. The existence of a patient with unilateral MCDK with normal renal function might provide genetic insight into the etiology of these substantial populations of only unilateral MCDK. The recurrent microdeletions encompassing HNF1B could have a significant impact on the mechanism of HNF1B deletions.
肝细胞核因子 1β(HNF1β)异常已被认为会导致肾脏和泌尿道先天性异常(CAKUT),主要影响双侧肾脏畸形。为了进一步了解 HNF1β 相关表型的范围,我们对 31 例肾发育不全(n = 31)、14 例单侧多囊性发育不良肾(MCDK;n = 14)和其他疾病(n = 5)的日本患者进行了 HNF1B 基因突变和缺失分析。我们在 50 例患者中的 5 例(10%)中发现了 HNF1B 改变。3 例单侧 MCDK 患者存在新生杂合性完全 HNF1B 缺失。其中 2 例患者对侧存在发育不全,而另 1 例患者对侧肾脏影像学正常,肾功能正常。拷贝数变异分析显示,存在涉及整个 HNF1B 基因的 1.4 Mb 微缺失,断裂点位于侧翼片段重复。我们还在双侧发育不全的患者中发现了 1 个新的截断突变(1007insC)和另一个错义突变(226G>T)。导致单倍体功能不全的 HNF1B 改变会影响到广泛的 CAKUT 谱。单侧 MCDK 患者肾功能正常的存在可能为这些单侧 MCDK 大量人群的病因提供遗传见解。包含 HNF1B 的复发性微缺失可能对 HNF1B 缺失的机制有重大影响。