Human folliculin delays cell cycle progression through late S and G2/M-phases: effect of phosphorylation and tumor associated mutations

• Published in: PloS one 2013-07, Vol.8 (7), p.e66775-e66775
• Main Authors: Laviolette, Laura A, Wilson, Jonas, Koller, Julia, Neil, Christopher, Hulick, Peter, Rejtar, Tomas, Karger, Barry, Teh, Bin Tean, Iliopoulos, Othon
• Format: Article
• Language: English
• Subjects: Animals; Biology; Bone disorder agents; Cancer; Carcinoma, Renal Cell - genetics; Carcinoma, Renal Cell - metabolism; Cell cycle; Cell Division - genetics; Cell Line, Tumor; Cells (Biology); Cysts; Embryo fibroblasts; Embryos; Estrone - genetics; Estrone - metabolism; Fibroblasts; Fibroblasts - metabolism; Flox; G2 Phase - genetics; Gene mutation; Genetic aspects; Genetic engineering; Genetic polymorphisms; Germ-Line Mutation; Hematology; Humans; Kidney cancer; Kidney Neoplasms - genetics; Kidney Neoplasms - metabolism; Laboratories; Lungs; Medical research; Medicine; Mice; Mutants; Mutation; Nocodazole; Oncology; Penicillin; Phosphorylation; Proteins; Reintroduction; Renal cell carcinoma; Tumor suppressor genes; Tumor Suppressor Proteins - genetics; Tumor Suppressor Proteins - metabolism; Tumors
• ISSN: 1932-6203; 1932-6203
• DOI: 10.1371/journal.pone.0066775

The Birt-Hogg-Dube disease occurs as a result of germline mutations in the human Folliculin gene (FLCN), and is characterized by clinical features including fibrofolliculomas, lung cysts and multifocal renal neoplasia. Clinical and genetic evidence suggest that FLCN acts as a tumor suppressor gene. The human cell line UOK257, derived from the renal cell carcinoma of a patient with a germline mutation in the FLCN gene, harbors a truncated version of the FLCN protein. Reconstitution of the wild type FLCN protein into UOK257 cells delays cell cycle progression, due to a slower progression through the late S and G2/M-phases. Similarly, Flcn (-/-) mouse embryonic fibroblasts progress more rapidly through the cell cycle than wild type controls (Flcn (flox/flox)). The reintroduction of tumor-associated FLCN mutants (FLCN ΔF157, FLCN 1-469 or FLCN K508R) fails to delay cell cycle progression in UOK257 cells. Additionally, FLCN phosphorylation (on Serines 62 and 73) fluctuates throughout the cell cycle and peaks during the G2/M phase in cells treated with nocodazole. In keeping with this observation, the reintroduction of a FLCN phosphomimetic mutant into the UOK257 cell line results in faster progression through the cell cycle compared to those expressing the wild type FLCN protein. These findings suggest that the tumor suppression function of FLCN may be linked to its impact on the cell cycle and that FLCN phosphorylation is important for this activity. Additionally, these observations describe a novel in vitro assay for testing the functional significance of FLCN mutations and/or genetic polymorphisms.