4.6 Article

KLIF-associated cytoskeletal proteins in Trypanosoma brucei regulate cytokinesis by promoting cleavage furrow positioning and ingression

Journal

JOURNAL OF BIOLOGICAL CHEMISTRY
Volume 298, Issue 6, Pages -

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ELSEVIER
DOI: 10.1016/j.jbc.2022.101943

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Funding

  1. National Institutes of Health, United States [AI101437, AI118736]
  2. Clinical and Translational Proteomics Service Center at University of Texas Health Science Center at Houston, United States

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This study investigates the role of the orphan kinesin KLIF in cleavage furrow ingression and identifies a group of cytoskeletal proteins associated with KLIF as essential regulators of cytokinesis. Depletion of KLIF impairs the resolution of the nascent posterior of the old-flagellar daughter cell, leading to a blockade of cleavage furrow ingression. Proximity biotinylation further identifies a subset of cytoskeleton-associated proteins as KLIF-proximal proteins, with CAP46 and CAP52 crucial for positioning the cleavage furrow while CAP42 and CAP50 promote furrow ingression.
Cytokinesis in the early divergent protozoan Trypanosoma brucei occurs from the anterior cell tip of the new-flagellum daughter toward the nascent posterior end of the oldflagellum daughter of a dividing biflagellated cell. The cleavage furrow ingresses unidirectionally along the preformed cell division fold and is regulated by an orphan kinesin named kinesin localized to the ingressing furrow (KLIF) that localizes to the leading edge of the ingressing furrow. Little is known about how furrow ingression is controlled by KLIF and whether KLIF interacts with and cooperates with other cytokinesis regulatory proteins to promote furrow ingression. Here, we investigated the roles of KLIF in cleavage furrow ingression and identified a cohort of KLIF-associated cytoskeletal proteins as essential cytokinesis regulators. By genetic complementation, we demonstrated the requirement of the kinesin motor activity, but not the putative tropomyosin domain, of KLIF in promoting furrow ingression. We further showed that depletion of KLIF impaired the resolution of the nascent posterior of the old-flagellar daughter cell, thereby stalking cleavage furrow ingression at late stages of cytokinesis. Through proximity biotinylation, we identified a subset of cytoskeleton-associated proteins (CAPs) as KLIF-proximal proteins, and functional characterization of these cytoskeletal proteins revealed the essential roles of CAP46 and CAP52 in positioning the cleavage furrow and the crucial roles of CAP42 and CAP50 in promoting cleavage furrow ingression. Together, these results identified multiple cytoskeletal proteins as cytokinesis regulators and uncovered their essential and distinct roles in cytokinesis.

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