Department of Plastic and Reconstructive Surgery and Hand Surgery, Erasmus MC, University Medical Center Rotterdam, Rotterdam, The Netherlands.
Department of Bioengineering and Therapeutic Sciences, University of California-San Francisco, San Francisco, California, USA.
Genet Med. 2018 Nov;20(11):1405-1413. doi: 10.1038/gim.2018.18. Epub 2018 Mar 15.
The zone of polarizing activity regulatory sequence (ZRS) is an enhancer that regulates sonic hedgehog during embryonic limb development. Recently, mutations in a noncoding evolutionary conserved sequence 500 bp upstream of the ZRS, termed the pre-ZRS (pZRS), have been associated with polydactyly in dogs and humans. Here, we report the first case of triphalangeal thumb-polysyndactyly syndrome (TPT-PS) to be associated with mutations in this region and show via mouse enhancer assays how this mutation leads to ectopic expression throughout the developing limb bud.
We used linkage analysis, whole-exome sequencing, Sanger sequencing, fluorescence in situ hybridization, multiplex ligation-dependent probe amplification, single-nucleotide polymorphism array, and a mouse transgenic enhancer assay.
Ten members of a TPT-PS family were included in this study. The mutation was linked to chromosome 7q36 (LOD score 3.0). No aberrations in the ZRS could be identified. A point mutation in the pZRS (chr7:156585476G>C; GRCh37/hg19) was detected in all affected family members. Functional characterization using a mouse transgenic enhancer essay showed extended ectopic expression dispersed throughout the entire limb bud (E11.5).
Our work describes the first mutation in the pZRS to be associated with TPT-PS and provides functional evidence that this mutation leads to ectopic expression of this enhancer within the developing limb.
极性活动调节序列(ZRS)是一个增强子,在胚胎肢发育过程中调节 sonic hedgehog。最近,在 ZRS 上游 500bp 的非编码进化保守序列中发现的突变,称为前 ZRS(pZRS),与犬和人类的多指畸形有关。在这里,我们报告了首例与该区域突变相关的三叉状拇指多指并指综合征(TPT-PS),并通过小鼠增强子实验展示了这种突变如何导致整个发育中的肢芽异位表达。
我们使用连锁分析、全外显子组测序、Sanger 测序、荧光原位杂交、多重连接依赖性探针扩增、单核苷酸多态性微阵列和小鼠转基因增强子实验。
本研究共纳入了 10 名 TPT-PS 家族成员。该突变与 7q36 染色体(LOD 评分 3.0)连锁。在 ZRS 中未发现异常。在所有受影响的家族成员中均检测到 pZRS 中的点突变(chr7:156585476G>C;GRCh37/hg19)。使用小鼠转基因增强子实验进行功能表征显示,异位表达扩展到整个肢芽(E11.5)。
我们的工作描述了首例与 TPT-PS 相关的 pZRS 突变,并提供了功能证据,证明该突变导致该增强子在发育中的肢内异位表达。