Folliculin directs the formation of a Rab34–RILP complex to control the nutrient‐dependent dynamic distribution of lysosomes
Autor: | Starling, Georgina P, Yip, Yan Y, Sanger, Anneri, Morton, Penny E, Eden, Emily R, Dodding, Mark P |
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Jazyk: | angličtina |
Rok vydání: | 2016 |
Předmět: |
Estrone
Gene Expression Golgi Apparatus folliculin Article Cell Line Proto-Oncogene Proteins Journal Article Humans Membrane & Intracellular Transport Adaptor Proteins Signal Transducing Tumor Suppressor Proteins Nuclear Proteins Articles Intracellular Membranes Recombinant Proteins Protein Transport Metabolism Rab34 rab GTP-Binding Proteins lysosome BHD syndrome RILP Carrier Proteins Lysosomes Protein Binding Signal Transduction |
Zdroj: | EMBO Reports Starling, G P, Yip, Y Y, Sanger, A, Morton, P E, Eden, E R & Dodding, M P 2016, ' Folliculin directs the formation of a Rab34-RILP complex to control the nutrient-dependent dynamic distribution of lysosomes ', EMBO Reports, vol. 17, no. 6, pp. 823-841 . https://doi.org/10.15252/embr.201541382 |
ISSN: | 1469-3178 1469-221X |
DOI: | 10.15252/embr.201541382 |
Popis: | The spatial distribution of lysosomes is important for their function and is, in part, controlled by cellular nutrient status. Here, we show that the lysosome associated Birt–Hoge–Dubé (BHD) syndrome renal tumour suppressor folliculin (FLCN) regulates this process. FLCN promotes the peri‐nuclear clustering of lysosomes following serum and amino acid withdrawal and is supported by the predominantly Golgi‐associated small GTPase Rab34. Rab34‐positive peri‐nuclear membranes contact lysosomes and cause a reduction in lysosome motility and knockdown of FLCN inhibits Rab34‐induced peri‐nuclear lysosome clustering. FLCN interacts directly via its C‐terminal DENN domain with the Rab34 effector RILP. Using purified recombinant proteins, we show that the FLCN‐DENN domain does not act as a GEF for Rab34, but rather, loads active Rab34 onto RILP. We propose a model whereby starvation‐induced FLCN association with lysosomes drives the formation of contact sites between lysosomes and Rab34‐positive peri‐nuclear membranes that restrict lysosome motility and thus promote their retention in this region of the cell. |
Databáze: | OpenAIRE |
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