Department of Pediatrics, Dell Pediatric Research Institute, University of Texas at Austin Dell Medical School, Austin, TX, USA.
Departments of Molecular and Cellular Biology and Medicine, Baylor College of Medicine, Houston, TX, USA.
Hum Mol Genet. 2019 Jan 15;28(2):200-208. doi: 10.1093/hmg/ddy339.
Spina bifida (SB) is a complex disorder of failed neural tube closure during the first month of human gestation, with a suspected etiology involving multiple gene and environmental interactions. GPR161 is a ciliary G-protein coupled receptor that regulates Sonic Hedgehog (Shh) signaling. Gpr161 null and hypomorphic mutations cause neural tube defects (NTDs) in mouse models. Herein we show that several genes involved in Shh and Wnt signaling were differentially expressed in the Gpr161 null embryos using RNA-seq analysis. To determine whether there exists an association between GPR161 and SB in humans, we performed direct Sanger sequencing on the GPR161 gene in a cohort of 384 SB patients and 190 healthy controls. We identified six rare variants of GPR161 in six SB cases, of which two of the variants were novel and did not exist in any databases. Both of these variants were predicted to be damaging by SIFT and/or PolyPhen analysis. The novel GPR161 rare variants mislocalized to the primary cilia, dysregulated Shh and Wnt signaling and inhibited cell proliferation in vitro. Our results demonstrate that GPR161 mutations cause NTDs via dysregulation of Shh and Wnt signaling in mice, and novel rare variants of GPR161 can be risk factors for SB in humans.
脊髓裂(SB)是一种在人类妊娠第一个月期间神经管闭合失败的复杂疾病,其发病机制涉及多个基因和环境相互作用。GPR161 是一种纤毛 G 蛋白偶联受体,可调节 Sonic Hedgehog(Shh)信号。Gpr161 缺失和功能降低突变会导致小鼠模型中的神经管缺陷(NTDs)。在此,我们通过 RNA-seq 分析表明,Gpr161 缺失胚胎中涉及 Shh 和 Wnt 信号的几个基因表达存在差异。为了确定 GPR161 是否与人类 SB 存在关联,我们在 384 名 SB 患者和 190 名健康对照者的 GPR161 基因中进行了直接 Sanger 测序。我们在 6 例 SB 病例中发现了 GPR161 的 6 种罕见变异,其中 2 种是新的,不存在于任何数据库中。这两种变异都被 SIFT 和/或 PolyPhen 分析预测为有害。新型 GPR161 罕见变异导致初级纤毛定位异常,Shh 和 Wnt 信号失调,并抑制体外细胞增殖。我们的研究结果表明,GPR161 突变通过在小鼠中失调 Shh 和 Wnt 信号导致 NTDs,新型 GPR161 罕见变异可能是人类 SB 的风险因素。