Folliculin – A tumor suppressor at the intersection of metabolic signaling and membrane traffic
Open accessAbstract
The Birt-Hoge-Dubé syndrome tumor suppressor Folliculin is a regulator of metabolism and has as a wide range of cellular and organismal phenotypes associated with its disruption. However, the molecular mechanisms which underlie its functions are poorly understood. Folliculin has been described to associate with lysosomes in response to nutrient depletion and form a key part of the signaling network that controls the activity of mTORC1. We recently reported that Folliculin can control the nutrient dependent cytoplasmic distribution of lysosomes by promoting the formation of a complex with the Golgi-associated small GTPase Rab34 and its effector RILP. We thus define a mechanistic connection between the lysosomal nutrient signaling network and the transport machinery that controls the distribution and dynamics of this organelle. Here we summarise the main conclusions from that study, attempt to integrate our findings with other recent studies on lysosome distribution/dynamics, and discuss the potential consequences of the dysregulation of this processes caused by Folliculin loss for Birt-Hoge-Dubé syndrome and normal cell function.
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A growing body of work supports an intrinsic role of FLCN and its associated interacting proteins in regulating lysosome positioning in response to cellular metabolism.
“It is intriguing to note that a growing body of work also supports the intrinsic role of FLCN and its associated interacting proteins in regulating lysosome positioning in response to cellular metabolism (Starling et al., 2016; Dodding, 2017).”
From Signal integration in the (m)TORC1 growth pathway (2018) · cites this paper as Dodding, 2017
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References 50 · Cited by 8
- Authors
- Dodding, M. P.
- Affiliations
- King's College London (GB)
- Corresponding author
- Dodding, Mark P.
- ORCID
- Dodding, Mark P.
- Venue
- Small GTPases
- Publisher
- Informa UK Limited
- Published
- 2016-06-29
- Volume
- 8
- Issue
- 2
- Pages
- 100-105
- ISSN
- 2154-1248 (ISSN-L)
- 2154-1256
- PMC
- PMC5464117
- OpenAlex
- W2460743054
- Cited by
- 8
- References
- 50
- Citations by year
- 2024: 1 · 2023: 1 · 2021: 2 · 2020: 2 · 2019: 1 · 2018: 1
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Small GTPases (publishedVersion)
- Europe PMC (PubMed Central) (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Explore Bristol Research (acceptedVersion, other-oa)
- Bristol Research (University of Bristol) (submittedVersion, other-oa)
- Research Portal (King's College London) (submittedVersion)
- Funders
- Wellcome Trust (097316/Z/11/Z, /Z/11/Z, 097316)
- Directorate for Biological Sciences
- Biotechnology and Biological Sciences Research Council (BB/L006774/1)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Cellular transport and secretion
- Health Sciences › Medicine › Epidemiology › Autophagy in Disease and Therapy
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › PI3K/AKT/mTOR signaling in cancer
- Keywords
- folliculin, Birt-Hogg-Dubé syndrome, tumor suppressor, Rab34, RILP, mTORC1 signaling, nutrient signaling, membrane trafficking, metabolic signaling
- MeSH terms
- Cell Membrane, Humans, Lysosomes, Signal Transduction, Protein Transport, Tumor Suppressor Proteins
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