Regulation of Small GTPase Prenylation in the Nervous System
Abstract
Mevalonate pathway inhibitors have been extensively studied for their roles in cholesterol depletion and for inhibiting the prenylation and activation of various proteins. Inhibition of protein prenylation has potential therapeutic uses against neurological disorders, like neural cancers, neurodegeneration, and neurotramatic lesions. Protection against neurodegeneration and promotion of neuronal regeneration is regulated in large part by Ras superfamily small guanosine triphosphatases (GTPases), particularly the Ras, Rho, and Rab subfamilies. These proteins are prenylated to target them to cellular membranes. Prenylation can be specifically inhibited through altering the function of enzymes of the mevalonate pathway necessary for isoprenoid production and attachment to target proteins to elicit a variety of effects on neural cells. However, this approach does not address how prenylation affects a specific protein. This review focuses on the regulation of small GTPase prenylation, the different techniques to inhibit prenylation, and how this inhibition has affected neural cell processes.
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Small GTPases need post-translational modification to target them to cellular membranes and be active.
“All these small GTPase need post-translational modification to target them to cellular membranes and be active [16,17].”
From Brain Cholesterol Biosynthetic Pathway Is Altered in a Preclinical Model of Fragile X Syndrome (2022) · cites this paper as [16]
Cites
PROTEIN PRENYLATION: GENES, ENZYMES, TARGETS, AND FUNCTIONS
Schafer, W. R., & Rine, J. (1992) · Annual Review of Genetics · doi:10.1146/annurev.ge.26.120192.001233 · Cited by 377 · see citing works
van der Kant, R., Langness, V. F., Herrera, C. M., Williams, D. A., Fong, L. K., Leestemaker, Y., Steenvoorden, E., Rynearson, K. D., Brouwers, J. F., Helms, J. B., et al. (2019) · Cell Stem Cell · doi:10.1016/j.stem.2018.12.013 · Cited by 350 · see citing works
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RhoA Signaling in Neurodegenerative Diseases
Schmidt, S. I., Blaabjerg, M., Freude, K., & Meyer, M. (2022) · Cells · doi:10.3390/cells11091520 · Cited by 110 · see citing works
Brain Cholesterol Biosynthetic Pathway Is Altered in a Preclinical Model of Fragile X Syndrome
Parente, M., Tonini, C., Buzzelli, V., Carbone, E., Trezza, V., & Pallottini, V. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23063408 · Cited by 11 · see citing works
“All these small GTPase need posttranslational modification to target them to cellular membranes and be active [16,17].”
Background
- Authors
- Reddy, J. M., Raut, N. G. R., Seifert, J. L., & Hynds, D. L.
- Affiliations
- Texas Woman's University (US)
- Corresponding author
- Hynds, DiAnna L.
- Venue
- Molecular Neurobiology
- Published
- 2020-01-27
- Volume
- 57
- Issue
- 5
- Pages
- 2220-2231
- ISSN
- 0893-7648 (ISSN-L)
- 1559-1182
- OpenAlex
- W3002636413
- Cited by
- 23
- References
- 2
- Citations by year
- 2026: 2 · 2025: 2 · 2024: 3 · 2023: 2 · 2022: 8 · 2021: 2 · 2020: 4
- FWCI
- 0.38
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Molecular Neurobiology (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Texas Woman's University Department of Biology (none)
- Texas Woman's University Research Enhancement Program (none)
- Texas Woman's University Center for Student Research (none)
- Texas Woman's University Biology Summer Research Award (none)
- National Science Foundation (DUE0806963, DUE1154394)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Protein Kinase Regulation and GTPase Signaling
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Sphingolipid Metabolism and Signaling
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Cellular transport and secretion
- Keywords
- protein prenylation, small GTPases, Ras superfamily, isoprenoid biosynthesis, Rho GTPases, Rab GTPases, neurodegeneration, neuronal regeneration, neurotrauma, cholesterol depletion, membrane targeting
- MeSH terms
- Acyl Coenzyme A, Animals, Cell Membrane, Dimethylallyltranstransferase, Enzyme Activation, Humans, Methylation, Mevalonic Acid, Nerve Tissue Proteins, Protein Binding, Terpenes, Protein Prenylation, GTP Phosphohydrolases, Amino Acid Motifs, Biosynthetic Pathways
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