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Title:

Mutations in the deubiquitinase gene USP8 cause Cushing's disease.

Document type:
Journal Article; Research Support, Non-U.S. Gov't; Comparative Study; Article
Author(s):
Reincke, Martin; Sbiera, Silviu; Hayakawa, Akira; Theodoropoulou, Marily; Osswald, Andrea; Beuschlein, Felix; Meitinger, Thomas; Mizuno-Yamasaki, Emi; Kawaguchi, Kohei; Saeki, Yasushi; Tanaka, Keiji; Wieland, Thomas; Graf, Elisabeth; Saeger, Wolfgang; Ronchi, Cristina L; Allolio, Bruno; Buchfelder, Michael; Strom, Tim M; Fassnacht, Martin; Komada, Masayuki
Abstract:
Cushing's disease is caused by corticotroph adenomas of the pituitary. To explore the molecular mechanisms of endocrine autonomy in these tumors, we performed exome sequencing of 10 corticotroph adenomas. We found somatic mutations in the USP8 deubiquitinase gene in 4 of 10 adenomas. The mutations clustered in the 14-3-3 protein binding motif and enhanced the proteolytic cleavage and catalytic activity of USP8. Cleavage of USP8 led to increased deubiqutination of the EGF receptor, impairing its...     »
Journal title abbreviation:
Nat Genet
Year:
2015
Journal volume:
47
Journal issue:
1
Pages contribution:
31-8
Language:
eng
Fulltext / DOI:
doi:10.1038/ng.3166
Pubmed ID:
http://view.ncbi.nlm.nih.gov/pubmed/25485838
Print-ISSN:
1061-4036
TUM Institution:
Institut für Humangenetik
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