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编码R-spondin 4(RSPO4)的基因发生突变可导致遗传性无甲,RSPO4是一种参与Wnt信号传导的分泌蛋白。

The gene encoding R-spondin 4 (RSPO4), a secreted protein implicated in Wnt signaling, is mutated in inherited anonychia.

作者信息

Blaydon Diana C, Ishii Yoshiyuki, O'Toole Edel A, Unsworth Harriet C, Teh Muy-Teck, Rüschendorf Franz, Sinclair Claire, Hopsu-Havu Väinö K, Tidman Nicholas, Moss Celia, Watson Rosemarie, de Berker David, Wajid Muhammad, Christiano Angela M, Kelsell David P

机构信息

Centre for Cutaneous Research, Institute of Cell & Molecular Science, Queen Mary's School of Medicine and Dentistry, Queen Mary, University of London, Whitechapel, London E1 4AT, UK.

出版信息

Nat Genet. 2006 Nov;38(11):1245-7. doi: 10.1038/ng1883. Epub 2006 Oct 15.

Abstract

Anonychia and hyponychia congenita (OMIM 206800) are rare autosomal recessive conditions in which the only presenting phenotype is the absence or severe hypoplasia of all fingernails and toenails. After determining linkage to chromosome 20p13, we identified homozygous or compound heterozygous mutations in the gene encoding R-spondin 4 (RSPO4), a secreted protein implicated in Wnt signaling, in eight affected families. Rspo4 expression was specifically localized to developing mouse nail mesenchyme at embryonic day 15.5, suggesting a crucial role in nail morphogenesis.

摘要

先天性无甲和甲床发育不全(OMIM 206800)是罕见的常染色体隐性疾病,其唯一的表现型是所有手指甲和脚趾甲缺失或严重发育不全。在确定与20号染色体p13区域连锁后,我们在8个患病家族中,于编码R-spondin 4(RSPO4)的基因中鉴定出纯合或复合杂合突变,RSPO4是一种参与Wnt信号传导的分泌蛋白。在胚胎第15.5天,Rspo4表达特异性定位于发育中的小鼠指甲间充质,提示其在指甲形态发生中起关键作用。

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