A Rho GTPase-effector ensemble governs cell migration behavior

How can a cell navigate its environment without any external cues? Since such cues are not always present in the environment, cells rely on internal machinery to explore their surroundings. Although Rho GTPases are known for orchestrating cell motility, the intrinsic Rho GTPase-effector mechanisms governing spontaneous migration remain incompletely understood. Here we show an imaging-based method that profiles protein-protein interactions (PPIs) through phase-separated condensates. By applying this method to hundreds of interaction profiles between Rho small GTPases and their effector proteins, we uncovered two intrinsic mechanisms governing cell migration. Formin-like protein (FMNL) determines the front of the cell by restricting Cdc42 activity, establishing front-rear polarity. In contrast, Rac1-ROCK-interaction-mediated arc stress fiber formation at the front inherently enables spontaneous directional changes and enhances cellular responses to external cues. Our findings elucidate the intricate roles of the Rho GTPase-effector ensemble that governs cell migration behavior, revealing an intrinsic program for efficient motility strategies.

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Publication Details

Journal
Nature Communications
Published
2025-10-31
DOI
https://doi.org/10.1038/s41467-025-64635-0
Citations
1
Primary Topic
Cellular Mechanics and Interactions
Type
article
Field-Weighted Citation Impact
1.15

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article

A Rho GTPase-effector ensemble governs cell migration behavior

Yohan Oh, Ho Min Kim, Kwang‐Hyun Cho, Gabsang Lee et al.
1 citations
Nature Communications
Cellular Mechanics and Interactions
1.15
article

A Rho GTPase-effector ensemble governs cell migration behavior

Yohan Oh, Ho Min Kim, Kwang‐Hyun Cho, Gabsang Lee, Bobae Hyeon, Yeji Seo, Dongsan Kim, Won Do Heo, Sangkyu Lee, Hyun‐Jun Kim, Yong Jin Lee, Young-Hyun Han, Hee‐Young Lee, Juae Jin
article en
1 citations

Abstract

How can a cell navigate its environment without any external cues? Since such cues are not always present in the environment, cells rely on internal machinery to explore their surroundings. Although Rho GTPases are known for orchestrating cell motility, the intrinsic Rho GTPase-effector mechanisms governing spontaneous migration remain incompletely understood. Here we show an imaging-based method that profiles protein-protein interactions (PPIs) through phase-separated condensates. By applying this method to hundreds of interaction profiles between Rho small GTPases and their effector proteins, we uncovered two intrinsic mechanisms governing cell migration. Formin-like protein (FMNL) determines the front of the cell by restricting Cdc42 activity, establishing front-rear polarity. In contrast, Rac1-ROCK-interaction-mediated arc stress fiber formation at the front inherently enables spontaneous directional changes and enhances cellular responses to external cues. Our findings elucidate the intricate roles of the Rho GTPase-effector ensemble that governs cell migration behavior, revealing an intrinsic program for efficient motility strategies.

Nature CommunicationsVol. 16(1)
Johns Hopkins University (US), Korea Advanced Institute of Science and Technology (KR), Johns Hopkins Medicine (US), Institute for Basic Science (KR), Lux Research (United States) (US), Hanyang University (KR)
National Research Foundation, National Research Foundation of Korea, Ministry of Science and ICT, South Korea, Samsung Science and Technology Foundation, Samsung
Openalex Percentile: Top 18%
Cellular Mechanics and Interactions
1.15
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