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Updated: May 15, 2026

Aip1p Dynamics Are Altered by the R256H Mutation in Actin
Published on: July 30, 2014
ARHGAP18 complexes with both YAP and Merlin and is required for basal actin bundles
Emma C Murray1, Gillian M Hodge1, Khanh Pham2
1Department of Biochemistry, State University of New York at Buffalo, Buffalo 14203 NY.
The Hippo and RhoA pathways coordinate cell structure. ARHGAP18 links these pathways, and its loss disrupts the actin cytoskeleton and cell signaling.
Area of Science:
- Cell Biology
- Molecular Biology
- Biochemistry
Background:
- Cytoskeletal filament organization relies on signaling cascades.
- Rho family GTPases and the Hippo pathway are key regulators of the actin cytoskeleton.
- These pathways influence cell morphology, actin structures, and are implicated in cancer progression.
Purpose of the Study:
- Investigate the interplay between Hippo and Rho Family signaling pathways in human epithelial cells.
- Characterize the role of ARHGAP18 in connecting these two signaling networks.
- Elucidate the impact of ARHGAP18 loss on cytoskeletal organization and YAP localization.
Main Methods:
- CRISPR/CAS9 gene editing to knockout ARHGAP18.
- Super-resolution STORM microscopy to analyze cytoskeletal changes at the single-filament level.
- Co-immunoprecipitation to identify protein complex formation.
Main Results:
- ARHGAP18 forms a complex with Hippo pathway components Merlin (NF2) and YAP.
- Loss of ARHGAP18 leads to actin cytoskeleton alterations.
- ARHGAP18 knockout results in RhoA signaling dysregulation and aberrant nuclear YAP localization.
Conclusions:
- ARHGAP18 acts as a crucial link between RhoA and Hippo signaling pathways.
- Coordinated regulation of the actin cytoskeleton by Hippo and Rho GTPase signaling is supported.
- Findings provide insights into cytoskeletal control and potential cancer mechanisms.
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