Tension promotes kinetochore-microtubule release by Aurora B kinase.


Journal

The Journal of cell biology
ISSN: 1540-8140
Titre abrégé: J Cell Biol
Pays: United States
ID NLM: 0375356

Informations de publication

Date de publication:
07 06 2021
Historique:
received: 06 07 2020
revised: 06 02 2021
accepted: 24 03 2021
entrez: 27 4 2021
pubmed: 28 4 2021
medline: 12 10 2021
Statut: ppublish

Résumé

To ensure accurate chromosome segregation, interactions between kinetochores and microtubules are regulated by a combination of mechanics and biochemistry. Tension provides a signal to discriminate attachment errors from bi-oriented kinetochores with sisters correctly attached to opposite spindle poles. Biochemically, Aurora B kinase phosphorylates kinetochores to destabilize interactions with microtubules. To link mechanics and biochemistry, current models regard tension as an input signal to locally regulate Aurora B activity. Here, we show that the outcome of kinetochore phosphorylation depends on tension. Using optogenetics to manipulate Aurora B at individual kinetochores, we find that kinase activity promotes microtubule release when tension is high. Conversely, when tension is low, Aurora B activity promotes depolymerization of kinetochore-microtubules while maintaining attachment. Thus, phosphorylation converts a catch-bond, in which tension stabilizes attachments, to a slip-bond, which releases microtubules under tension. We propose that tension is a signal inducing distinct error-correction pathways, with release or depolymerization being advantageous for typical errors characterized by high or low tension, respectively.

Identifiants

pubmed: 33904910
pii: 212027
doi: 10.1083/jcb.202007030
pmc: PMC8082439
pii:
doi:

Substances chimiques

TNS1 protein, human 0
Tensins 0
AURKB protein, human EC 2.7.11.1
Aurora Kinase B EC 2.7.11.1

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : NIGMS NIH HHS
ID : R01 GM118510
Pays : United States
Organisme : NIGMS NIH HHS
ID : R35 GM122475
Pays : United States
Organisme : NIGMS NIH HHS
ID : R35 GM130298
Pays : United States
Organisme : NCI NIH HHS
ID : U54 CA193417
Pays : United States

Informations de copyright

© 2021 Chen et al.

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Auteurs

Geng-Yuan Chen (GY)

Department of Biology, School of Arts and Sciences, University of Pennsylvania, Philadelphia, PA.

Fioranna Renda (F)

Wadsworth Center, New York State Department of Health, Albany, NY.

Huaiying Zhang (H)

Department of Biology, School of Arts and Sciences, University of Pennsylvania, Philadelphia, PA.

Alper Gokden (A)

Department of Biology, School of Arts and Sciences, University of Pennsylvania, Philadelphia, PA.

Daniel Z Wu (DZ)

Department of Chemistry, School of Arts and Sciences, University of Pennsylvania, Philadelphia, PA.

David M Chenoweth (DM)

Department of Chemistry, School of Arts and Sciences, University of Pennsylvania, Philadelphia, PA.

Alexey Khodjakov (A)

Wadsworth Center, New York State Department of Health, Albany, NY.

Michael A Lampson (MA)

Department of Biology, School of Arts and Sciences, University of Pennsylvania, Philadelphia, PA.

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Classifications MeSH