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Phenotypic expansion of POFUT1 loss of function mutations in a disorder featuring segmental dyspigmentation with eczematous and folliculo‐centric lesions
Author(s) -
Atzmony Lihi,
Zaki Theodore D.,
Antaya Richard J.,
Choate Keith A.
Publication year - 2019
Publication title -
american journal of medical genetics part a
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.064
H-Index - 112
eISSN - 1552-4833
pISSN - 1552-4825
DOI - 10.1002/ajmg.a.61362
Subject(s) - frameshift mutation , biology , phenotype , loss of heterozygosity , genetics , mutation , germline , exome sequencing , germline mutation , gene , allele
Appearance of mosaic disorders in thin Blaschko lines suggests that somatic mutations in keratinocyte precursors underlie their pathogenesis. Germline heterozygous mutations in POFUT1 gene cause Dowling–Degos disease (DDD), a skin disease that features flexural reticulated hyperpigmentation and follicular‐based lesions. POFUT1 mosaicism has not been described to date. Here, we describe a 9‐year‐old female with segmental hyper‐ and hypopigmented patches with overlying eczematous plaques and follicular papules. Employing paired whole exome sequencing of saliva and keratinocytes isolated from affected skin, we found a novel germline heterozygous POFUT1 deletion causing frameshift and premature codon termination and somatic copy‐neutral loss of heterozygosity on chromosome 20 encompassing POFUT1 . Expression levels of POFUT1 as well as other key regulators of the notch signaling pathway— NOTCH1 , NOTCH2 , and HES1 —were reduced in affected keratinocytes compared with normal keratinocytes. Our findings provide the first evidence of POFUT1 postzygotic mutation and a phenotypic expansion of POFUT1 loss of function mutations. We show that a recessive loss of function mutation in POFUT1 produces a distinct clinical presentation with features (e.g., dermatitis) that are absent in the generalized form of DDD. This study demonstrates how analysis of mosaic disorders can reveal unexpected phenotypes for known genes.