Department of Clinical Science and Education, Södersjukhuset, Karolinska Institutet, Stockholm, Sweden.
Hum Mutat. 2012 Jul;33(7):1063-6. doi: 10.1002/humu.22097. Epub 2012 May 11.
Mutations in the Sonic hedgehog limb enhancer, the zone of polarizing activity regulatory sequence (ZRS, located within the gene LMBR1), commonly called the ZRS), cause limb malformations. In humans, three classes of mutations have been proposed based on the limb phenotype; single base changes throughout the region cause preaxial polydactyly (PPD), single base changes at one specific site cause Werner mesomelic syndrome, and large duplications cause polysyndactyly. This study presents a novel mutation-a small insertion. In a Swedish family with autosomal-dominant PPD, we found a 13 base pair insertion within the ZRS, NG_009240.1:g.106934_106935insTAAGGAAGTGATT (traditional nomenclature: ZRS603ins13). Computational transcription factor-binding site predictions suggest that this insertion creates new binding sites and a mouse enhancer assay shows that this insertion causes ectopic gene expression. This study is the first to discover a small insertion in an enhancer that causes a human limb malformation and suggests a potential mechanism that could explain the ectopic expression caused by this mutation.
Sonic hedgehog 肢芽增强子(位于 LMBR1 基因内的极性活动调节序列 (ZRS))中的突变通常被称为 ZRS),可导致肢体畸形。在人类中,根据肢体表型提出了三类突变;整个区域的单个碱基变化导致前轴多指(PPD),一个特定部位的单个碱基变化导致 Werner 中胚层综合征,而大片段重复则导致并指。本研究提出了一种新的突变——小插入。在一个瑞典常染色体显性 PPD 家族中,我们发现 ZRS 内有一个 13 碱基对的插入,NG_009240.1:g.106934_106935insTAAGGAAGTGATT(传统命名法:ZRS603ins13)。计算转录因子结合位点预测表明,该插入产生了新的结合位点,而小鼠增强子试验表明该插入导致异位基因表达。本研究首次发现了一个导致人类肢体畸形的增强子中的小插入,并提出了一种可能的机制,可以解释该突变引起的异位表达。