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Sephardic origins revealed for rare skin disorder, recessive dystrophic epidermolysis bullosa, in individuals carrying the unique c.6527insC mutation.

Sephardic origins revealed for rare skin disorder, recessive dystrophic epidermolysis bullosa, in individuals carrying the unique c.6527insC mutation. Journal of medical genetics Warshauer, E. M., Maier, P. A., Runfeldt, G., Fuentes, I., Escamez, M. J., Valinotto, L., Natale, M., Manzur, G., Illera, N., Garcia, M., Del Rio, M., Mencia, A., Holguin, A., Larcher, F., Hellenthal, G., Brown, A. R., Consuegra, L., Rivera, C., Nogueiro, I., Tang, J., Oro, A., Marinkovich, P., Palisson, F., Titeux, M., Hovnanian, A. A., Sprecher, E., Skorecki, K., Norris, D., Bruckner, A., Kogut, I., Bilousova, G., Roop, D. 2025

Abstract

Recessive dystrophic epidermolysis bullosa (RDEB) is a rare and severe blistering skin disorder caused by loss-of-function mutations in the type VII collagen gene (COL7A1). The COL7A1 c.6527insC mutation is curiously prevalent among individuals with RDEB and is found worldwide in Europe and the Americas. Previous research has suggested the possibility of a Sephardic Jewish origin of the mutation; however, individuals with RDEB are not known to have predominant Jewish ancestry.In this study, a global cohort of individuals with RDEB with the c.6527insC founder mutation from Spain, France, Argentina, Chile, Colombia and the USA were investigated by autosomal genotyping, pairwise identical-by-descent matching and a local ancestry analysis. Age estimation analysis was performed to determine when Jewish founders introduced the c.6527insC mutation into Iberian and Native American populations (~900?CE and 1492 CE, respectively).Sephardic ancestry was identified at the haplotype spanning the c.6527insC mutation in 85% of the individuals, despite mixed ancestry elsewhere in the genome and no known recent Sephardic ancestry. Identical-by-descent matching between this RDEB subpopulation and a known crypto-Jewish community in Belmonte, Portugal was also ascertained, providing support for crypto-Jewish ancestry in this RDEB subpopulation.The identification of this unique RDEB subpopulation unified by the single most prevalent c.6527insC mutation holds great potential to facilitate promising new RDEB therapies using CRISPR Cas 9 gene and base editing. The identification of a single guide RNA allowing efficient and safe editing of this variant would represent a unique drug to treat a large cohort of patients with the same founder mutation.

View details for DOI 10.1136/jmg-2025-110967

View details for PubMedID 40992924