Publication — IRIC

Rab11FIP1 maintains Rab35 at the intercellular bridge to promote actin removal and abscission.

Cytokinesis occurs at the end of mitosis/meiosis wherein the cytoplasms of daughter cells are separated. Prior to abscission, an intercellular bridge containing the remaining furrowing machinery, mitotic spindle and actin cytoskeleton connects the two daughter cells. To remove this actin and allow for separation of daughter cells, Rab35 vesicles, loaded with the actin oxidizer MICAL1 and the inositol polyphosphate 5-phosphatase OCRL are recruited to the midbody in a fine-tuned spatiotemporal manner. Importantly however, the means by which these vesicles are recruited is currently unclear. Here, we demonstrate that Rab11FIP1 is recruited to the midbody after Rab35 to scaffold it at the bridge and maintain Rab35 in this region. In the absence of Rab11FIP1, Rab35 dramatically drops from the midbody, inducing defects such as cytokinetic delays and binucleation due to actin overaccumulation at the intercellular bridge, defects which can be rescued with Latrunculin A treatment. Importantly, we show that Rab11FIP1 is critical for Rab35 function in actin removal prior to cytokinesis.

Date de publication
27 mai 2021
Chercheurs
Iannantuono NVG, Emery G
Référence PubMed
J Cell Sci 2021
ID PubMed
34043006
Affiliation
Institute for Research in Immunology and Cancer (IRIC), Université de Montréal, Montréal, Québec, Canada.