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TPXL-1 activates Aurora A to clear contractile ring components from the polar cortex during cytokinesis

During cytokinesis, a signal from the central spindle that forms 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 th...

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Autores principales: Mangal, Sriyash, Sacher, Jennifer, Kim, Taekyung, Osório, Daniel Sampaio, Motegi, Fumio, Carvalho, Ana Xavier, Oegema, Karen, Zanin, Esther
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Rockefeller University Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5839786/
https://www.ncbi.nlm.nih.gov/pubmed/29311228
http://dx.doi.org/10.1083/jcb.201706021
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author Mangal, Sriyash
Sacher, Jennifer
Kim, Taekyung
Osório, Daniel Sampaio
Motegi, Fumio
Carvalho, Ana Xavier
Oegema, Karen
Zanin, Esther
author_facet Mangal, Sriyash
Sacher, Jennifer
Kim, Taekyung
Osório, Daniel Sampaio
Motegi, Fumio
Carvalho, Ana Xavier
Oegema, Karen
Zanin, Esther
author_sort Mangal, Sriyash
collection PubMed
description During cytokinesis, a signal from the central spindle that forms 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.
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spelling pubmed-58397862018-09-05 TPXL-1 activates Aurora A to clear contractile ring components from the polar cortex during cytokinesis Mangal, Sriyash Sacher, Jennifer Kim, Taekyung Osório, Daniel Sampaio Motegi, Fumio Carvalho, Ana Xavier Oegema, Karen Zanin, Esther J Cell Biol Research Articles During cytokinesis, a signal from the central spindle that forms 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. The Rockefeller University Press 2018-03-05 /pmc/articles/PMC5839786/ /pubmed/29311228 http://dx.doi.org/10.1083/jcb.201706021 Text en © 2018 Mangal et al. http://www.rupress.org/terms/https://creativecommons.org/licenses/by-nc-sa/4.0/This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms/). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 International license, as described at https://creativecommons.org/licenses/by-nc-sa/4.0/).
spellingShingle Research Articles
Mangal, Sriyash
Sacher, Jennifer
Kim, Taekyung
Osório, Daniel Sampaio
Motegi, Fumio
Carvalho, Ana Xavier
Oegema, Karen
Zanin, Esther
TPXL-1 activates Aurora A to clear contractile ring components from the polar cortex during cytokinesis
title TPXL-1 activates Aurora A to clear contractile ring components from the polar cortex during cytokinesis
title_full TPXL-1 activates Aurora A to clear contractile ring components from the polar cortex during cytokinesis
title_fullStr TPXL-1 activates Aurora A to clear contractile ring components from the polar cortex during cytokinesis
title_full_unstemmed TPXL-1 activates Aurora A to clear contractile ring components from the polar cortex during cytokinesis
title_short TPXL-1 activates Aurora A to clear contractile ring components from the polar cortex during cytokinesis
title_sort tpxl-1 activates aurora a to clear contractile ring components from the polar cortex during cytokinesis
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5839786/
https://www.ncbi.nlm.nih.gov/pubmed/29311228
http://dx.doi.org/10.1083/jcb.201706021
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