Localization and function of Arf family GTPases
Abstract
Arfs are a family of Ras-related GTP-binding proteins that function in the regulation of membrane trafficking and structure. The six mammalian Arf proteins are expressed ubiquitously and so it is anticipated that each will have a distinct localization and function within the cell. It has been assumed that much of this specificity will be defined by determining which regulators of Arfs, the GEFs (guanine nucleotide-exchange factors) and GAPs (GTPase-activating proteins) function with which Arf proteins. Although in vitro assays may indicate Arf preferences for the numerous Arf GEFs and GAPs that have been identified, in the cell the different Arfs, GEFs and GAPs are targeted to specific compartments where they carry out their functions. We have embarked on studies to define regions of the Arf1 and Arf6 proteins that determine their sites of action and specific activities at the Golgi and plasma membrane respectively. Chimaeras were made between Arf1 and Arf6 in order to identify regions of the protein that contributed to targeting and function. Whereas Arf6 is targeted to the plasma membrane through multiple regions along the protein, we have found a Golgi-targeting region in Arf1 that is sufficient to target Arf6 to the Golgi complex.
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ARFs are a large family of ras-related GTPases that regulate membrane trafficking and organelle structure.
“ARFs are a large family of ras-related GTPases that regulate membrane trafficking and organelle structure (For review see [72]).”
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Higdon, C. W., Mitra, R. D., & Johnson, S. L. (2013) · PLoS ONE · doi:10.1371/journal.pone.0067801 · Cited by 125 · see citing works
Schlienger, S., Ramirez, R. A. M., & Claing, A. (2015) · Cellular Signalling · doi:10.1016/j.cellsig.2014.11.032 · Cited by 50 · see citing works
- Authors
- Donaldson, J. G., & Honda, A.
- Affiliations
- National Institutes of Health (US)
- Venue
- Biochemical Society Transactions
- Publisher
- Portland Press Ltd.
- Published
- 2005-08-01
- Volume
- 33
- Issue
- 4
- Pages
- 639-642
- ISSN
- 0300-5127 (ISSN-L)
- 1470-8752
- OpenAlex
- W2028273808
- Cited by
- 170
- References
- 0
- Citations by year
- 2026: 1 · 2025: 2 · 2024: 3 · 2023: 3 · 2022: 4 · 2021: 5 · 2020: 2 · 2019: 6 · 2018: 7 · 2017: 17 · 2016: 7 · 2015: 7 · 2014: 8 · 2013: 9 · 2012: 11
- FWCI
- 0.94
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Biochemical Society Transactions (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Cellular transport and secretion
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Protein Kinase Regulation and GTPase Signaling
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Fungal and yeast genetics research
- Keywords
- Arf GTPases, Arf1, ARF6, Golgi targeting, plasma membrane targeting, fusion protein, membrane trafficking, guanine nucleotide exchange factor, GTPase-activating protein, Golgi apparatus, subcellular localization
- MeSH terms
- ADP-Ribosylation Factor 6, Amino Acid Sequence, Animals, Drosophila melanogaster, Golgi Apparatus, Humans, Molecular Sequence Data, Sequence Alignment, Conserved Sequence, Sequence Homology, Amino Acid, ADP-Ribosylation Factors, ADP-Ribosylation Factor 1, Drosophila Proteins
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