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Update of cylindromatosis gene ( CYLD ) mutations in Brooke‐Spiegler syndrome: novel insights into the role of deubiquitination in cell signaling
Author(s) -
Blake Patrick W.,
Toro Jorge R.
Publication year - 2009
Publication title -
human mutation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.981
H-Index - 162
eISSN - 1098-1004
pISSN - 1059-7794
DOI - 10.1002/humu.21024
Subject(s) - biology , germline , genetics , deubiquitinating enzyme , gene , mutation , exon , germline mutation , signal transducing adaptor protein , ubiquitin , microbiology and biotechnology , cancer research
Abstract Germline mutations in the cylindromatosis ( CYLD ) gene have been described in families with cylindromas, trichoepitheliomas, and/or spiradenomas. Brooke‐Spiegler syndrome (BSS) is the autosomal dominant predisposition to skin appendageal neoplasms including cylindromas, trichoepitheliomas, and/or spiradenomas. We review the clinical features, molecular genetics, and the animal models of BSS. To date, a total of 51 germline CYLD mutations have been reported, occurring in exons 9–20, in 73 families with diverse ethnic and racial backgrounds. Of 51 mutations, 86% are expected to lead to truncated proteins. The seven missense mutations reported to date occur only within the ubiquitin (Ub)‐specific protease (USP) domain of the CYLD protein and most are associated exclusively with multiple familial trichoepithelioma (MFT). CYLD functions as a tumor suppressor gene. CYLD encodes a deubiquitinating (DUB) enzyme that negatively regulates the nuclear factor (NF)‐κB and c‐Jun N‐terminal kinase (JNK) pathways. CYLD DUB activity is highly specific for lysine 63 (K63)‐linked Ub chains but has been shown to act on K48‐linked Ub chains as well. In 2008, the CYLD USP domain was crystallized, revealing that the truncated Fingers subdomain confers CYLD's unique specificity for K63‐linked Ub chains. Recent work using animal models revealed new roles for CYLD in immunity, lipid metabolism, spermatogenesis, osteoclastogenesis, antimicrobial defense, and inflammation. Hum Mutat 30:1–12, 2009. Published 2009 Wiley‐Liss, Inc.