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The mitotic spindle protein CKAP2 potently increases formation and stability of microtubules

Cells increase microtubule dynamics to make large rearrangements to their microtubule cytoskeleton during cell division. Changes in microtubule dynamics are essential for the formation and function of the mitotic spindle, and misregulation can lead to aneuploidy and cancer. Using in vitro reconstitu...

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Detalles Bibliográficos
Autores principales: McAlear, Thomas S, Bechstedt, Susanne
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8798059/
https://www.ncbi.nlm.nih.gov/pubmed/35029146
http://dx.doi.org/10.7554/eLife.72202
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author McAlear, Thomas S
Bechstedt, Susanne
author_facet McAlear, Thomas S
Bechstedt, Susanne
author_sort McAlear, Thomas S
collection PubMed
description Cells increase microtubule dynamics to make large rearrangements to their microtubule cytoskeleton during cell division. Changes in microtubule dynamics are essential for the formation and function of the mitotic spindle, and misregulation can lead to aneuploidy and cancer. Using in vitro reconstitution assays we show that the mitotic spindle protein Cytoskeleton-Associated Protein 2 (CKAP2) has a strong effect on nucleation of microtubules by lowering the critical tubulin concentration 100-fold. CKAP2 increases the apparent rate constant k(a) of microtubule growth by 50-fold and increases microtubule growth rates. In addition, CKAP2 strongly suppresses catastrophes. Our results identify CKAP2 as the most potent microtubule growth factor to date. These finding help explain CKAP2’s role as an important spindle protein, proliferation marker, and oncogene.
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spelling pubmed-87980592022-01-31 The mitotic spindle protein CKAP2 potently increases formation and stability of microtubules McAlear, Thomas S Bechstedt, Susanne eLife Biochemistry and Chemical Biology Cells increase microtubule dynamics to make large rearrangements to their microtubule cytoskeleton during cell division. Changes in microtubule dynamics are essential for the formation and function of the mitotic spindle, and misregulation can lead to aneuploidy and cancer. Using in vitro reconstitution assays we show that the mitotic spindle protein Cytoskeleton-Associated Protein 2 (CKAP2) has a strong effect on nucleation of microtubules by lowering the critical tubulin concentration 100-fold. CKAP2 increases the apparent rate constant k(a) of microtubule growth by 50-fold and increases microtubule growth rates. In addition, CKAP2 strongly suppresses catastrophes. Our results identify CKAP2 as the most potent microtubule growth factor to date. These finding help explain CKAP2’s role as an important spindle protein, proliferation marker, and oncogene. eLife Sciences Publications, Ltd 2022-01-14 /pmc/articles/PMC8798059/ /pubmed/35029146 http://dx.doi.org/10.7554/eLife.72202 Text en © 2022, McAlear and Bechstedt https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Biochemistry and Chemical Biology
McAlear, Thomas S
Bechstedt, Susanne
The mitotic spindle protein CKAP2 potently increases formation and stability of microtubules
title The mitotic spindle protein CKAP2 potently increases formation and stability of microtubules
title_full The mitotic spindle protein CKAP2 potently increases formation and stability of microtubules
title_fullStr The mitotic spindle protein CKAP2 potently increases formation and stability of microtubules
title_full_unstemmed The mitotic spindle protein CKAP2 potently increases formation and stability of microtubules
title_short The mitotic spindle protein CKAP2 potently increases formation and stability of microtubules
title_sort mitotic spindle protein ckap2 potently increases formation and stability of microtubules
topic Biochemistry and Chemical Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8798059/
https://www.ncbi.nlm.nih.gov/pubmed/35029146
http://dx.doi.org/10.7554/eLife.72202
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