Mutations in POGLUT1, encoding protein o-glucosyltransferase 1, cause autosomal-dominant Dowling-Degos disease

Item Type:	Article
Title:	Mutations in POGLUT1, encoding protein o-glucosyltransferase 1, cause autosomal-dominant Dowling-Degos disease
Creators Name:	Basmanav, F.B. and Oprisoreanu, A.M. and Pasternack, S.M. and Thiele, H. and Fritz, G. and Wenzel, J. and Größer, L. and Wehner, M. and Wolf, S. and Fagerberg, C. and Bygum, A. and Altmüller, J. and Rütten, A. and Parmentier, L. and El Shabrawi-Caelen, L. and Hafner, C. and Nürnberg, P. and Kruse, R. and Schoch, S. and Hanneken, S. and Betz, R.C.
Abstract:	Dowling-Degos disease (DDD) is an autosomal-dominant genodermatosis characterized by progressive and disfiguring reticulate hyperpigmentation. We previously identified loss-of-function mutations in KRT5 but were only able to detect pathogenic mutations in fewer than half of our subjects. To identify additional causes of DDD, we performed exome sequencing in five unrelated affected individuals without mutations in KRT5. Data analysis identified three heterozygous mutations from these individuals, all within the same gene. These mutations, namely c.11G>A (p.Trp4∗), c.652C>T (p.Arg218∗), and c.798-2A>C, are within POGLUT1, which encodes protein O-glucosyltransferase 1. Further screening of unexplained cases for POGLUT1 identified six additional mutations, as well as two of the above described mutations. Immunohistochemistry of skin biopsies of affected individuals with POGLUT1 mutations showed significantly weaker POGLUT1 staining in comparison to healthy controls with strong localization of POGLUT1 in the upper parts of the epidermis. Immunoblot analysis revealed that translation of either wild-type (WT) POGLUT1 or of the protein carrying the p.Arg279Trp substitution led to the expected size of about 50 kDa, whereas the c.652C>T (p.Arg218∗) mutation led to translation of a truncated protein of about 30 kDa. Immunofluorescence analysis identified a colocalization of the WT protein with the endoplasmic reticulum and a notable aggregating pattern for the truncated protein. Recently, mutations in POFUT1, which encodes protein O-fucosyltransferase 1, were also reported to be responsible for DDD. Interestingly, both POGLUT1 and POFUT1 are essential regulators of Notch activity. Our results furthermore emphasize the important role of the Notch pathway in pigmentation and keratinocyte morphology.
Keywords:	DNA Sequence Analysis, Exome, Genetic Skin Diseases, Genome-Wide Association Study, Glucosyltransferases, Heterozygote, Hyperpigmentation, Keratinocytes, Mutation, Papulosquamous Skin Diseases, Pedigree, Protein Conformation, Skin, Young Adult
Source:	American Journal of Human Genetics
ISSN:	0002-9297
Publisher:	Cell Press
Volume:	94
Number:	1
Page Range:	135-143
Date:	2 January 2014
Official Publication:	https://doi.org/10.1016/j.ajhg.2013.12.003
PubMed:	View item in PubMed

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