Gustavsson Peter, Greene Nicholas D E, Lad Dina, Pauws Erwin, de Castro Sandra C P, Stanier Philip, Copp Andrew J
Neural Development Unit, Institute of Child Health, University College London, Guilford Street, London WC1N 1EH, UK.
Hum Mol Genet. 2007 Nov 1;16(21):2640-6. doi: 10.1093/hmg/ddm221. Epub 2007 Aug 24.
Neural tube defects (NTDs), such as spina bifida, are common and severe birth defects in humans but the underlying causes are poorly understood. The pathogenesis and etiology of spina bifida in the curly tail mouse closely resemble defects in humans, providing a well-characterized model of NTDs. Grainyhead-like-3 (Grhl3), which encodes a transcription factor, was recently identified as a candidate gene for curly tail based on chromosomal location and the occurrence of spina bifida in Grhl3 null mice. However, the causative curly tail mutation has not been established, while the relationship between Grhl3 gene expression and the known cellular defect leading to NTDs in curly tail is unknown. Spina bifida in curly tail results from a cell type-specific proliferation defect in the hindgut endoderm, and we find that Grhl3 is expressed specifically in this tissue during the final stages of spinal neural tube closure in wild type embryos. Moreover, Grhl3 expression is diminished in the spinal region of neurulation-stage curly tail embryos. Curly tail mice do not carry a coding region mutation in Grhl3, however, we found a putative regulatory mutation upstream of the Grhl3 gene, which may be responsible for the expression deficit. In order to test the hypothesis that spina bifida in curly tail mice results from insufficient expression of Grhl3, we generated Grhl3-expressing curly tail mice by bacterial artificial chromosome-mediated transgenesis and demonstrated complete rescue of spina bifida. This study provides evidence for a critical role of diminished Grhl3 expression in causing spinal NTDs in the curly tail mouse model.
神经管缺陷(如脊柱裂)是人类常见且严重的出生缺陷,但其根本原因尚不清楚。卷尾小鼠脊柱裂的发病机制和病因与人类缺陷极为相似,为神经管缺陷提供了一个特征明确的模型。颗粒头样蛋白3(Grhl3)编码一种转录因子,基于染色体定位以及Grhl3基因敲除小鼠中脊柱裂的发生情况,它最近被确定为卷尾的候选基因。然而,导致卷尾的致病突变尚未明确,同时Grhl3基因表达与导致卷尾小鼠神经管缺陷的已知细胞缺陷之间的关系也不清楚。卷尾小鼠的脊柱裂是由后肠内胚层细胞类型特异性增殖缺陷引起的,我们发现野生型胚胎在脊髓神经管闭合的最后阶段,Grhl3在该组织中特异性表达。此外,在神经胚形成阶段的卷尾胚胎的脊髓区域,Grhl3表达减少。卷尾小鼠在Grhl3中没有编码区突变,然而,我们在Grhl3基因上游发现了一个推定的调控突变,这可能是导致表达缺陷的原因。为了验证卷尾小鼠脊柱裂是由Grhl3表达不足引起的这一假设,我们通过细菌人工染色体介导的转基因技术构建了表达Grhl3的卷尾小鼠,并证明脊柱裂得到了完全挽救。这项研究为Grhl3表达减少在卷尾小鼠模型中导致脊髓神经管缺陷的关键作用提供了证据。