TPXL-1 activates Aurora A to clear contractile ring components from the polar cortex during cytokinesis
Year: 2018
Type: article
Abstract: ABSTRACT During cytokinesis, a signal from the bundled microtubules that form between the separating anaphase chromosomes promotes the accumulation of contractile ring components at the cell equator, while a signal from the centrosomal microtubule asters inhibits accumulation of contractile ring components at the cell poles. However, the molecular identity of the inhibitory signal has remained unknown. To identify molecular components of the aster-based inhibitory signal, we developed a means to monitor the removal of contractile ring proteins from the polar cortex after anaphase onset. Using this assay, we show that polar clearing is an active process that requires activation of Aurora A kinase by TPXL-1. TPXL-1 concentrates on astral microtubules coincident with polar clearing in anaphase, and its ability to recruit Aurora A and activate its kinase activity are essential for clearing. In summary, our data identify Aurora A kinase as an aster-based inhibitory signal that restricts contractile ring components to the cell equator during cytokinesis. SUMMARY During cytokinesis, centrosomal asters inhibit cortical contractility at the cell poles. Mangal et al. provide molecular insight into this phenomenon, showing that TPXL-1, which localizes to astral microtubules, activates Aurora A kinase to clear contractile ring proteins from the polar cortex.
Source: The Journal of Cell Biology
Authors: Sriyash Mangal, Jennifer Sacher, Taekyung Kim, Daniel Sampaio Osório, Fumio Motegi, Ana Xavier Carvalho, Karen Oegema, Esther Zanin
Institutions: Center for Integrated Protein Science Munich, Ludwig-Maximilians-Universität München, University of California San Diego, Ludwig Cancer Research, Universidade do Porto, i3S - Instituto de Investigação e Inovação em Saúde, Universidade do Porto, Instituto de Biologia Molecular e Celular, National University of Singapore
Language: English
Subfield: Cell Biology
Domain: Life Sciences
Open Access status: hybrid
Funders: Ludwig Institute for Cancer Research, International Max Planck Research School for Environmental, Cellular and Molecular Microbiology, Deutsche Forschungsgemeinschaft, International Max Planck Research School for Advanced Methods in Process and Systems Engineering, National Institutes of Health, National Institute of General Medical Sciences, H2020 European Research Council
OpenAlex ID: W2763852829
