| Literature DB >> 31082376 |
Steffen Hörer1, Slaheddine Marrakchi2, Franz P W Radner3, Gerd Zolles4, Lisa Heinz5, Thomas O Eichmann6, Cristina Has7, Pavel Salavei8, Nadia Mahfoudh9, Hamida Turki2, Andreas D Zimmer5, Judith Fischer10.
Abstract
Trichilemmal cysts are common hair follicle-derived intradermal cysts. The trait shows an autosomal dominant mode of transmission with incomplete penetrance. Here, we describe the pathogenetic mechanism for the development of hereditary trichilemmal cysts. By whole-exome sequencing of DNA from the blood samples of 5 affected individuals and subsequent Sanger sequencing of a family cohort including 35 affected individuals, this study identified a combination of the Phospholipase C Delta 1 germline variants c.903A>G, p.(Pro301Pro) and c.1379C>T, p.(Ser460Leu) as a high-risk factor for trichilemmal cyst development. Allele-specific PCRs and cloning experiments showed that these two variants are present on the same allele. The analysis of tissue from several cysts revealed that an additional somatic Phospholipase C Delta 1 mutation on the same allele is required for cyst formation. In two different functional in vitro assays, this study showed that the protein function of the cyst-specific 1-phosphatidylinositol 4, 5-bisphosphate phosphodiesterase delta-1 protein variant is modified. This pathologic mechanism defines a monoallelic model of the two-hit mechanism proposed for tumor development and other hereditary cyst diseases.Entities:
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Year: 2019 PMID: 31082376 DOI: 10.1016/j.jid.2019.04.015
Source DB: PubMed Journal: J Invest Dermatol ISSN: 0022-202X Impact factor: 8.551