Institute for Biomedical Sciences, George Washington University, Washington, District of Columbia, USA.
FASEB J. 2011 May;25(5):1596-605. doi: 10.1096/fj.10-169771. Epub 2011 Feb 3.
Polydactyly is a common malformation and can be an isolated anomaly or part of a pleiotropic syndrome. The elucidation of the mutated genes that cause polydactyly provides insight into limb development pathways. The extra-toes spotting (Xs) mouse phenotype manifests anterior polydactyly, predominantly in the forelimbs, with ventral hypopigmenation. The mapping of Xs(J) to chromosome 7 was confirmed, and the interval was narrowed to 322 kb using intersubspecific crosses. Two mutations were identified in eukaryotic translation initiation factor 3 subunit C (Eif3c). An Eif3c c.907C>T mutation (p.Arg303X) was identified in Xs(J), and a c.1702_1758del mutation (p.Leu568_Leu586del) was identified in extra-toes spotting-like (Xsl), an allele of Xs(J). The effect of the Xs(J) mutation on the SHH/GLI3 pathway was analyzed by in situ hybridization analysis, and we show that Xs mouse embryos have ectopic Shh and Ptch1 expression in the anterior limb. In addition, anterior limb buds show aberrant Gli3 processing, consistent with perturbed SHH/GLI3 signaling. Based on the occurrence of Eif3c mutations in 2 Xs lines and haploinsufficiency of the Xs(J) allele, we conclude that the Xs phenotype is caused by a mutation in Eif3c, a component of the translation initiation complex, and that the phenotype is associated with aberrant SHH/GLI3 signaling.
多指畸形是一种常见的畸形,可作为孤立的异常,也可作为多效性综合征的一部分。阐明导致多指畸形的突变基因,为肢体发育途径提供了深入的了解。额外趾斑点(Xs)小鼠表型表现为前多指畸形,主要发生在前肢,并伴有腹侧色素减退。Xs(J)被映射到 7 号染色体,通过亚种间杂交将间隔缩小到 322 kb。在真核翻译起始因子 3 亚基 C(Eif3c)中鉴定出两个突变。Xs(J)中发现了 Eif3c c.907C>T 突变(p.Arg303X),Xs 样(Xsl)中发现了 c.1702_1758del 突变(p.Leu568_Leu586del),Xsl 是 Xs(J)的等位基因。通过原位杂交分析,分析了 Xs(J)突变对 SHH/GLI3 途径的影响,我们发现 Xs 小鼠胚胎在前肢中具有异位 Shh 和 Ptch1 表达。此外,前肢芽显示异常 Gli3 加工,与 SHH/GLI3 信号传导紊乱一致。基于 2 个 Xs 系中 Eif3c 突变的发生和 Xs(J)等位基因的单倍不足,我们得出结论,Xs 表型是由翻译起始复合物的组成部分 Eif3c 的突变引起的,并且表型与异常的 SHH/GLI3 信号传导有关。