Crystal structure of folliculin reveals a hidDENN function in genetically inherited renal cancer
Author(s) -
Ravi K. Nookala,
Lars Langemeyer,
A. Pacitto,
Bernardo OchoaMontaño,
Jane C. Donaldson,
Beata K. Blaszczyk,
Dimitri Y. Chirgadze,
Francis A. Barr,
J. Fernando Bazán,
Tom L. Blundell
Publication year - 2012
Publication title -
open biology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.078
H-Index - 53
ISSN - 2046-2441
DOI - 10.1098/rsob.120071
Subject(s) - folliculin , biology , mutation , guanine nucleotide exchange factor , microbiology and biotechnology , suppressor , cancer , cancer research , genetics , gtpase , gene
Mutations in the renal tumour suppressor protein, folliculin, lead to proliferative skin lesions, lung complications and renal cell carcinoma. Folliculin has been reported to interact with AMP-activated kinase, a key component of the mammalian target of rapamycin pathway. Most cancer-causing mutations lead to a carboxy-terminal truncation of folliculin, pointing to a functional importance of this domain in tumour suppression. We present here the crystal structure of folliculin carboxy-terminal domain and demonstrate that it is distantly related to differentially expressed in normal cells and neoplasia (DENN) domain proteins, a family of Rab guanine nucleotide exchange factors (GEFs). Using biochemical analysis, we show that folliculin has GEF activity, indicating that folliculin is probably a distantly related member of this class of Rab GEFs.
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