Phosphoinositide-mediated ring anchoring resists perpendicular forces to promote medial cytokinesis

Author:

Snider Chloe E.1,Willet Alaina H.1ORCID,Chen Jun-Song1,Arpağ Göker1,Zanic Marija1ORCID,Gould Kathleen L.1ORCID

Affiliation:

1. Department of Cell and Developmental Biology, Vanderbilt University, Nashville, TN

Abstract

Many eukaryotic cells divide by assembling and constricting an actin- and myosin-based contractile ring (CR) that is physically linked to the plasma membrane (PM). In this study, we report that Schizosaccharomyces pombe cells lacking efr3, which encodes a conserved PM scaffold for the phosphatidylinositol-4 kinase Stt4, build CRs that can slide away from the cell middle during anaphase in a myosin V–dependent manner. The Efr3-dependent CR-anchoring mechanism is distinct from previously reported pathways dependent on the Fes/CIP4 homology Bin-Amphiphysin-Rvs167 (F-BAR) protein Cdc15 and paxillin Pxl1. In efr3Δ, the concentrations of several membrane-binding proteins were reduced in the CR and/or on the PM. Our results suggest that proper PM lipid composition is important to stabilize the central position of the CR and resist myosin V–based forces to promote the fidelity of cell division.

Funder

National Institutes of Health

American Heart Association

Human Frontier Science Program

Publisher

Rockefeller University Press

Subject

Cell Biology

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