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小GTP酶Cdc42的脂化作用作为其生理和病理生理功能的调节因子

Lipidation of small GTPase Cdc42 as regulator of its physiological and pathophysiological functions.

作者信息

Wirth Alexander, Ponimaskin Evgeni

机构信息

Cellular Neurophysiology, Hannover Medical School, Hannover, Germany.

出版信息

Front Physiol. 2023 Jan 9;13:1088840. doi: 10.3389/fphys.2022.1088840. eCollection 2022.


DOI:10.3389/fphys.2022.1088840
PMID:36699687
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9868626/
Abstract

The protein cell division cycle 42 (Cdc42) is a small GTPase of the Rho family regulating a plethora of physiological functions in a tissue, cell and subcellular-specific manner participating in multiple signaling pathways. Since the corresponding signaling hubs are mainly organized along the cellular membranes, cytosolic proteins like Cdc42 need to be properly targeted and held at the membrane. Here, lipid modifications come into play: Cdc42 can be associated with membranes by different lipid anchors including prenylation (Cdc42-prenyl) and palmitoylation (Cdc42-palm). While Cdc42-prenyl is ubiquitously expressed, Cdc42-palm splicing variant in mainly expressed in the brain. Mechanisms underlying Cdc42 lipidation as well as its regulation are the main topic of this review. Furthermore, we will discuss the functional importance of Cdc42 lipid modifications with the focus on the role of different lipids in regulating defined Cdc42 functions. Finally, we will provide an overview of the possible implementation of Cdc42 lipidation in pathological conditions and different diseases.

摘要

蛋白质细胞分裂周期42(Cdc42)是Rho家族的一种小GTP酶,以组织、细胞和亚细胞特异性方式调节多种生理功能,参与多个信号通路。由于相应的信号枢纽主要沿细胞膜组织,像Cdc42这样的胞质蛋白需要正确靶向并固定在膜上。在此,脂质修饰发挥作用:Cdc42可通过不同的脂质锚定与膜相关联,包括异戊二烯化(Cdc42-异戊二烯)和棕榈酰化(Cdc42-棕榈酰)。虽然Cdc42-异戊二烯广泛表达,但Cdc42-棕榈酰剪接变体主要在大脑中表达。Cdc42脂化及其调节的潜在机制是本综述的主要主题。此外,我们将讨论Cdc42脂质修饰的功能重要性,重点关注不同脂质在调节特定Cdc42功能中的作用。最后,我们将概述Cdc42脂化在病理状况和不同疾病中的可能应用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/037d/9868626/c92063eecbf5/fphys-13-1088840-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/037d/9868626/ab065695365c/fphys-13-1088840-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/037d/9868626/c92063eecbf5/fphys-13-1088840-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/037d/9868626/ab065695365c/fphys-13-1088840-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/037d/9868626/c92063eecbf5/fphys-13-1088840-g002.jpg

相似文献

[1]
Lipidation of small GTPase Cdc42 as regulator of its physiological and pathophysiological functions.

Front Physiol. 2023-1-9

[2]
Dual lipidation of the brain-specific Cdc42 isoform regulates its functional properties.

Biochem J. 2013-12-15

[3]
Palmitoylation of the small GTPase Cdc42 by DHHC5 modulates spine formation and gene transcription.

J Biol Chem. 2022-6

[4]
Identification of a novel prenyl and palmitoyl modification at the CaaX motif of Cdc42 that regulates RhoGDI binding.

Mol Cell Biol. 2013-1-28

[5]
Selective axonal translation of the mRNA isoform encoding prenylated Cdc42 supports axon growth.

J Cell Sci. 2021-4-1

[6]
Monitoring RhoGDI Extraction of Lipid-Modified Rho GTPases from Membranes Using Click Chemistry.

Methods Mol Biol. 2019

[7]
Different roles of the small GTPases Rac1, Cdc42, and RhoG in CALEB/NGC-induced dendritic tree complexity.

J Neurochem. 2016-10

[8]
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J Biol Chem. 2005-4-8

[9]
Transforming activity of the Rho family GTPase, Wrch-1, a Wnt-regulated Cdc42 homolog, is dependent on a novel carboxyl-terminal palmitoylation motif.

J Biol Chem. 2005-9-23

[10]
New insights into how the Rho guanine nucleotide dissociation inhibitor regulates the interaction of Cdc42 with membranes.

J Biol Chem. 2009-8-28

引用本文的文献

[1]
CDC42 Regulates the ERK Pathway to Improve Oxygen‒Glucose Deprivation/Reoxygenation-Induced Neural Oxidative Stress and Apoptosis.

Mol Neurobiol. 2025-3-4

[2]
The influences of ARHGEF9 on myoblasts migration and differentiation.

J Muscle Res Cell Motil. 2025-2-24

[3]
Oleate Promotes Triple-Negative Breast Cancer Cell Migration by Enhancing Filopodia Formation through a PLD/Cdc42-Dependent Pathway.

Int J Mol Sci. 2024-4-2

本文引用的文献

[1]
The brain-specific splice variant of the CDC42 GTPase works together with the kinase ACK to downregulate the EGF receptor in promoting neurogenesis.

J Biol Chem. 2022-11

[2]
Protein Prenyltransferases and Their Inhibitors: Structural and Functional Characterization.

Int J Mol Sci. 2022-5-12

[3]
Palmitoylation of the small GTPase Cdc42 by DHHC5 modulates spine formation and gene transcription.

J Biol Chem. 2022-6

[4]
Trapping of CDC42 C-terminal variants in the Golgi drives pyrin inflammasome hyperactivation.

J Exp Med. 2022-6-6

[5]
Identification of substrates of palmitoyl protein thioesterase 1 highlights roles of depalmitoylation in disulfide bond formation and synaptic function.

PLoS Biol. 2022-3

[6]
Selective axonal translation of the mRNA isoform encoding prenylated Cdc42 supports axon growth.

J Cell Sci. 2021-4-1

[7]
The Growing Spectrum of Human Diseases Caused by Inherited CDC42 Mutations.

J Clin Immunol. 2020-5

[8]
A toxic palmitoylation of Cdc42 enhances NF-κB signaling and drives a severe autoinflammatory syndrome.

J Allergy Clin Immunol. 2020-11

[9]
The two splice variant forms of Cdc42 exert distinct and essential functions in neurogenesis.

J Biol Chem. 2020-2-18

[10]
S-acylated Golga7b stabilises DHHC5 at the plasma membrane to regulate cell adhesion.

EMBO Rep. 2019-8-12

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