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bioRxiv · 10.1101/2024.08.19.608523

Dimerization GAS2 mediates microtubule and F-actin crosslinking

Jiancheng, A.·Imasaki, T.·Narita, A.·Niwa, S.·Sasaki, R.·Makino, T.·Nitta, R.·Kikkawa, M.
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Abstract

GAS2 was originally identified as a growth arrest-specific protein, and recent studies have revealed its involvement in multiple cellular processes. Its dual interaction with actin filaments and microtubules highlights its essential role in cytoskeletal organization, such as cell division, apoptosis, and possibly tumorigenesis. However, the structural bases by which GAS2 regulates cytoskeletal dynamics remain unclear. In this study, we present cryo-EM structures of the GAS2- CH3 domain in complex with F-actin at 2.8 [A] resolution, representing the first type 3 CH domain structure bound to F-actin, confirming its actin-binding activity. We also provide the first near- atomic resolution cryo-EM structure of the GAS2-GAR domain bound to microtubules and identified conserved microtubule-binding residues. Our biochemical experiments show that GAS2 promotes microtubule nucleation and polymerization and its C-terminal region is essential for dimerization, bundling of both F-actin and microtubules, and microtubule nucleation. Based on these results, we propose how GAS2 controls cytoskeletal organization.

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Jiancheng, A., Imasaki, T., Narita, A., Niwa, S., Sasaki, R., Makino, T., Nitta, R., Kikkawa, M.. 2024-08-19. Dimerization GAS2 mediates microtubule and F-actin crosslinking. https://doi.org/10.1101/2024.08.19.608523

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