Stottmann R W, Bjork B C, Doyle J B, Beier D R
Genesis. 2010 May;48(5):303-8. doi: 10.1002/dvg.20618.
Mutations in Interferon Regulatory Factor 6 (IRF6) have been identified in two human allelic syndromes with cleft lip and/or palate: Van der Woude (VWS) and Popliteal Pterygium syndromes (PPS). Furthermore, common IRF6 haplotypes and single nucleotide polymorphisms (SNP) alleles are strongly associated with nonsyndromic clefting defects in multiple ethnic populations. Mutations in the mouse often provide good models for the study of human diseases and developmental processes. We identified the cleft palate 1 (clft1) mouse mutant in a forward genetic screen for phenotypes modeling human congenital disease. In the clft1 mutant, we have identified a novel missense point mutation in the mouse Irf6 gene, which confers an amino acid alteration that has been found in a VWS family. Phenotypic comparison of clft1 mutants to previously reported Irf6 mutant alleles demonstrates the Irf6(clft1) allele is a hypomorphic allele. The cleft palate seen in these mutants appears to be due to abnormal adhesion between the palate and tongue. The Irf6(clft1) allele provides the first mouse model for the study of an etiologic IRF6 missense mutation observed in a human VWS family.
在两种伴有唇裂和/或腭裂的人类等位基因综合征中已鉴定出干扰素调节因子6(IRF6)的突变:范德伍德综合征(VWS)和腘翼状胬肉综合征(PPS)。此外,常见的IRF6单倍型和单核苷酸多态性(SNP)等位基因与多个种族人群的非综合征性腭裂缺陷密切相关。小鼠中的突变通常为人类疾病和发育过程的研究提供良好的模型。我们在一个用于模拟人类先天性疾病表型的正向遗传筛选中鉴定出腭裂1(clft1)小鼠突变体。在clft1突变体中,我们在小鼠Irf6基因中鉴定出一个新的错义点突变,该突变导致了在一个VWS家族中发现的氨基酸改变。将clft1突变体与先前报道的Irf6突变等位基因进行表型比较表明,Irf6(clft1)等位基因是一个亚效等位基因。这些突变体中出现的腭裂似乎是由于腭与舌之间的异常粘连所致。Irf6(clft1)等位基因为研究在一个人类VWS家族中观察到的病因性IRF6错义突变提供了首个小鼠模型。