Human ITCH E3 Ubiquitin Ligase Deficiency Causes Syndromic Multisystem Autoimmune Disease
Author(s) -
Naomi J. Lohr,
Jean P. Molleston,
Kevin A. Strauss,
Wilfredo TorresMartinez,
Eric A. Sherman,
Robert H. Squires,
Nicholas L. Rider,
Kudakwashe Chikwava,
Oscar W. Cummings,
D. Holmes Morton,
Erik G. Puffenberger
Publication year - 2010
Publication title -
the american journal of human genetics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 6.661
H-Index - 302
eISSN - 1537-6605
pISSN - 0002-9297
DOI - 10.1016/j.ajhg.2010.01.028
Subject(s) - ubiquitin ligase , ubiquitin , medicine , disease , autoimmune disease , immunology , genetics , biology , gene
Ubiquitin ligases play an important role in the regulation of the immune system. Absence of Itch E3 ubiquitin ligase in mice has been shown to cause severe autoimmune disease. Using autozygosity mapping in a large Amish kindred, we identified a linkage region on chromosome 20 and selected candidate genes for screening. We describe, in ten patients, identification of a mutation resulting in truncation of ITCH. These patients represent the first reported human phenotype associated with ITCH deficiency. These patients not only have multisystem autoimmune disease but also display morphologic and developmental abnormalities. This disorder underscores the importance of ITCH ubiquitin ligase in many cellular processes.
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