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  Mutations in the deubiquitinase gene USP8 cause Cushing's disease

Reincke, M., Sbiera, S., Hayakawa, A., Theodoropoulou, M., Osswald, A., Beuschlein, F., et al. (2015). Mutations in the deubiquitinase gene USP8 cause Cushing's disease. NATURE GENETICS, 47(1), 31-+. doi:10.1038/ng.3166.

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 Creators:
Reincke, Martin1, Author
Sbiera, Silviu1, Author
Hayakawa, Akira1, Author
Theodoropoulou, Marily2, Author           
Osswald, Andrea1, Author
Beuschlein, Felix1, Author
Meitinger, Thomas1, Author
Mizuno-Yamasaki, Emi1, Author
Kawaguchi, Kohei1, Author
Saeki, Yasushi1, Author
Tanaka, Keiji1, Author
Wieland, Thomas1, Author
Graf, Elisabeth1, Author
Saeger, Wolfgang1, Author
Ronchi, Cristina L.1, Author
Allolio, Bruno1, Author
Buchfelder, Michael1, Author
Strom, Tim M.1, Author
Fassnacht, Martin1, Author
Komada, Masayuki1, Author
Affiliations:
1external, ou_persistent22              
2Clinical Research, Max Planck Institute of Psychiatry, Max Planck Society, ou_2035296              

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 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 downregulation and sustaining EGF signaling. USP8 mutants enhanced promoter activity of the gene encoding proopiomelanocortin. In summary, our data show that dominant mutations in USP8 cause Cushing's disease via activation of EGF receptor signaling.

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Language(s): eng - English
 Dates: 2015-01
 Publication Status: Issued
 Pages: -
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 Table of Contents: -
 Rev. Type: -
 Identifiers: ISI: 000346990400008
DOI: 10.1038/ng.3166
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Title: NATURE GENETICS
Source Genre: Journal
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Publ. Info: New York, NY 10013-1917 USA : Nature Publishing Group
Pages: - Volume / Issue: 47 (1) Sequence Number: - Start / End Page: 31 - + Identifier: ISSN: 1061-4036