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Nature Research, Nature Genetics, 5(46), p. 482-486, 2014

DOI: 10.1038/ng.2941

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Rare missense variants in POT1 predispose to familial cutaneous malignant melanoma

Journal article published in 2014 by Brigitte Bressac de Paillerets, Jianxin Shi, Yang Xr, Xiaohong R. Yang, Bari Ballew, Melissa Rotunno, Donato Calista, Fargnoli Mc, Maria Concetta Fargnoli, Paola Ghiorzo, Brigitte Bressac-De Paillerets, Avril Mf, Eduardo Nagore, Brigitte Bressac-De Paillerets, Caporaso Ne and other authors.
This paper is available in a repository.
This paper is available in a repository.

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Data provided by SHERPA/RoMEO

Abstract

Although CDKN2A is the most frequent high-risk melanoma susceptibility gene, the underlying genetic factors for most melanoma-prone families remain unknown. Using whole-exome sequencing, we identified a rare variant that arose as a founder mutation in the telomere shelterin gene POT1 (chromosome 7, g.124493086C>T; p.Ser270Asn) in five unrelated melanoma-prone families from Romagna, Italy. Carriers of this variant had increased telomere lengths and numbers of fragile telomeres, suggesting that this variant perturbs telomere maintenance. Two additional rare POT1 variants were identified in all cases sequenced in two separate Italian families, one variant per family, yielding a frequency for POT1 variants comparable to that for CDKN2A mutations in this population. These variants were not found in public databases or in 2,038 genotyped Italian controls. We also identified two rare recurrent POT1 variants in US and French familial melanoma cases. Our findings suggest that POT1 is a major susceptibility gene for familial melanoma in several populations.