Abstract
Hand-foot-genital syndrome (HFGS) is a rare autosomal dominant inherited syndrome characterized by limb malformations and urogenital defects. HFGS is caused by mutations in the HOXA13 gene. The aim of this study was to identify causative mutations in individuals and to explore the molecular pathogenesis in a Chinese family with HFGS. We performed Sanger sequencing and identified a recurrent missense mutation in the homeodomain (c.1123G>T, p.V375F) of HOXA13, molecular modelling predicted the mutation would affect DNA binding, and a luciferase reporter assay indicated that it impaired the ability of HOXA13 to activate transcription of the human EPHA7 promoter. This is the first report of the molecular basis for HFGS caused by missense mutations of HOXA13.
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Acknowledgements
This work was supported by the Natural Science Foundation of China (nos 81000253, 81670896) and the Specialized Research Fund for the Doctoral Programme of Higher Education of China (no. 20102104120024). We thank all the family members for their generous participation.
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Cao, L., Chen, C., Leng, Y. et al. A missense mutation of HOXA13 underlies hand-foot-genital syndrome in a Chinese family. J Genet 96, 647–652 (2017). https://doi.org/10.1007/s12041-017-0810-y
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DOI: https://doi.org/10.1007/s12041-017-0810-y