| Literature DB >> 24496061 |
Xue Wang1, Qian Xin1, Lin Li2, Jiangxia Li1, Changwu Zhang3, Rongfang Qiu1, Chenmin Qian4, Hailing Zhao1, Yongchao Liu1, Shan Shan1, Jie Dang1, Xianli Bian1, Changshun Shao1, Yaoqin Gong1, Qiji Liu1.
Abstract
Split-hand/foot malformation (SHFM) is a congenital limb deformity due to the absence or dysplasia of central rays of the autopod. Six SHFM loci have already been identified. Here we describe a Chinese family with autosomal-dominant SHFM1 that has previously been mapped to 7q21.2-21.3. The two affected family members, mother and son, showed deep median clefts between toes, ectrodactyly and syndactyly; the mother also showed triphalangeal thumbs. Exome sequencing and variant screening of candidate genes in the six loci known to be responsible for SHFM revealed a novel heterozygous mutation, c.558G>T (p.(Gln186His)), in distal-less homeobox 5 (DLX5). As DLX5 encodes a transcription factor capable of transactivating MYC, we also tested whether the mutation could affect DLX5 transcription acitivity. Results from luciferase reporter assay revealed that a mutation in DLX5 compromised its transcriptional activity. This is the first report of a mutation in DLX5 leading to autosomal-dominant SHFM1.Entities:
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Year: 2014 PMID: 24496061 PMCID: PMC4135423 DOI: 10.1038/ejhg.2014.7
Source DB: PubMed Journal: Eur J Hum Genet ISSN: 1018-4813 Impact factor: 4.246