期刊
MECHANISMS OF DEVELOPMENT
卷 127, 期 7-8, 页码 385-392出版社
ELSEVIER SCIENCE BV
DOI: 10.1016/j.mod.2009.12.002
关键词
Neural tube defects; VANGL genes; Convergent extension; Planar cell polarity; Zebrafish model
资金
- Canadian Institutes for Health Research [PG. MT-13425]
- SickKids Foundation
- Fonds de la Recherche en Sante du Quebec
- Natural Science and Engineering Research Council
- Genome Quebec
- Genome Canada
- Gaslini Foundation
- Telethon-Italy [GGP08051]
In humans, rare non-synonymous variants in the planar cell polarity gene VANGL1 are associated with neural tube defects (NTDs). These variants were hypothesized to be pathogenic based mainly on genetic studies in a large cohort of NTD patients. In this study, we validate the potential pathogenic effect of these mutations in vivo by investigating their effect on convergent extension in zebrafish. Knocking down the expression of tri, the ortholog of Vangl2, using an antisense morpholino (MO), as shown previously, led to a defective convergent extension (CE) manifested by a shortened body axis and widened somites. Co-injection of the human VANGL1 with the tri-MO was able to partially rescue the tri-MO induced phenotype in zebrafish. In contrast, co-injection of two human VANGL1 variants, p.Val239Ile and p.Met328Thr, failed to rescue this phenotype. We next carried out overexpression studies where we measured the ability of the human VANGL1 alleles to induce a CE phenotype when injected at high doses in zebrafish embryos. While overexpressing the wild-type allele led to a severely defective CE, overexpression of either p.Val239Ile or p.Met328Thr variant failed to do so. Results from both tri-MO knockdown/rescue results and overexpression assays suggest that these two variants most likely represent loss-of-function alleles that affect protein function during embryonic development. Our study demonstrates a high degree of functional conservation of VANGL genes across evolution and provides a model system for studying potential variants identified in human NTDs. (C) 2009 Elsevier Ireland Ltd. All rights reserved.
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