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The mammalian kinetochore–microtubule interface: robust mechanics and computation with many microtubules

Research output: Contribution to journal › Review article › peer-review

16 Scopus citations

Abstract

The kinetochore drives chromosome segregation at cell division. It acts as a physical link between chromosomes and dynamic microtubules, and as a signaling hub detecting and processing microtubule attachments to control anaphase onset. The mammalian kinetochore is a large macromolecular machine that forms a dynamic interface with the many microtubules that it binds. While we know most of the kinetochore's component parts, how they work together to give rise to its robust functions remains poorly understood. Here we highlight recent findings that shed light on this question, driven by an expanding physical and molecular toolkit. We present emerging principles that underlie the kinetochore's robust microtubule grip, such as redundancy, specialization, and dynamicity, and present signal processing principles that connect this microtubule grip to robust computation. Throughout, we identify open questions, and define simple engineering concepts that provide insight into kinetochore function.

Original languageEnglish
Pages (from-to)60-67
Number of pages8
JournalCurrent Opinion in Cell Biology
Volume60
DOIs
StatePublished - Oct 2019

Bibliographical note

Publisher Copyright:
© 2019 Elsevier Ltd

Funding

We thank Ted Salmon and many colleagues for stimulating discussions, and apologize for not acknowledging all relevant work due to space constraints. We thank the Dumont Lab for critical reading of the manuscript. This work was supported by National Institutes of Health DP2GM119177 (S.D), National Science Foundation CAREER 1554139 (S.D), the National Science Foundation Center for Cellular Construction DBI-1548297 (A.F.L, S.D.), a National Science Foundation Graduate Research Fellowship (A.F.L., J. K.), UCSF Moritz-Heyman Discovery Fellowships (A.F.L., J. K.), and a UCSF Lloyd Kozloff Fellowship (A.F.L.).

FundersFunder number
National Science Foundation Center for Cellular ConstructionDBI-1548297
National Science Foundation Arctic Social Science Program1554139
National Institutes of Health (NIH)
National Institute of General Medical Sciences DP2GM119177 Sophie Dumont National Institute of General Medical SciencesDP2GM119177
University of California San Francisco

    ASJC Scopus subject areas

    • Cell Biology

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