Cited by 23Protein Kinase Regulation and GTPase SignalingSphingolipid Metabolism and SignalingCellular transport and secretion

Regulation of Small GTPase Prenylation in the Nervous System

Reddy, Jairus M., Raut, Namrata G. R., Seifert, Jennifer L., Hynds, DiAnna L.·2020·Molecular Neurobiology

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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Crossref · 10.1007/s12035-020-01870-0

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2 of 2 references verified0 citation errors · 0 not checkable

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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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