Open Biology (Jan 2012)

Crystal structure of folliculin reveals a hidDENN function in genetically inherited renal cancer

  • Ravi K. Nookala,
  • Lars Langemeyer,
  • Angela Pacitto,
  • Bernardo Ochoa-Montaño,
  • Jane C. Donaldson,
  • Beata K. Blaszczyk,
  • Dimitri Y. Chirgadze,
  • Francis A. Barr,
  • J. Fernando Bazan,
  • Tom L. Blundell

DOI
https://doi.org/10.1098/rsob.120071
Journal volume & issue
Vol. 2, no. 8

Abstract

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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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