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Three-dimensional structure of kinetochore-fibers in human mitotic spindles

During cell division, kinetochore microtubules (KMTs) provide a physical linkage between the chromosomes and the rest of the spindle. KMTs in mammalian cells are organized into bundles, so-called kinetochore-fibers (k-fibers), but the ultrastructure of these fibers is currently not well characterize...

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Autores principales: Kiewisz, Robert, Fabig, Gunar, Conway, William, Baum, Daniel, Needleman, Daniel, Müller-Reichert, Thomas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9365394/
https://www.ncbi.nlm.nih.gov/pubmed/35894209
http://dx.doi.org/10.7554/eLife.75459
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author Kiewisz, Robert
Fabig, Gunar
Conway, William
Baum, Daniel
Needleman, Daniel
Müller-Reichert, Thomas
author_facet Kiewisz, Robert
Fabig, Gunar
Conway, William
Baum, Daniel
Needleman, Daniel
Müller-Reichert, Thomas
author_sort Kiewisz, Robert
collection PubMed
description During cell division, kinetochore microtubules (KMTs) provide a physical linkage between the chromosomes and the rest of the spindle. KMTs in mammalian cells are organized into bundles, so-called kinetochore-fibers (k-fibers), but the ultrastructure of these fibers is currently not well characterized. Here, we show by large-scale electron tomography that each k-fiber in HeLa cells in metaphase is composed of approximately nine KMTs, only half of which reach the spindle pole. Our comprehensive reconstructions allowed us to analyze the three-dimensional (3D) morphology of k-fibers and their surrounding MTs in detail. We found that k-fibers exhibit remarkable variation in circumference and KMT density along their length, with the pole-proximal side showing a broadening. Extending our structural analysis then to other MTs in the spindle, we further observed that the association of KMTs with non-KMTs predominantly occurs in the spindle pole regions. Our 3D reconstructions have implications for KMT growth and k-fiber self-organization models as covered in a parallel publication applying complementary live-cell imaging in combination with biophysical modeling (Conway et al., 2022). Finally, we also introduce a new visualization tool allowing an interactive display of our 3D spindle data that will serve as a resource for further structural studies on mitosis in human cells.
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spelling pubmed-93653942022-08-11 Three-dimensional structure of kinetochore-fibers in human mitotic spindles Kiewisz, Robert Fabig, Gunar Conway, William Baum, Daniel Needleman, Daniel Müller-Reichert, Thomas eLife Cell Biology During cell division, kinetochore microtubules (KMTs) provide a physical linkage between the chromosomes and the rest of the spindle. KMTs in mammalian cells are organized into bundles, so-called kinetochore-fibers (k-fibers), but the ultrastructure of these fibers is currently not well characterized. Here, we show by large-scale electron tomography that each k-fiber in HeLa cells in metaphase is composed of approximately nine KMTs, only half of which reach the spindle pole. Our comprehensive reconstructions allowed us to analyze the three-dimensional (3D) morphology of k-fibers and their surrounding MTs in detail. We found that k-fibers exhibit remarkable variation in circumference and KMT density along their length, with the pole-proximal side showing a broadening. Extending our structural analysis then to other MTs in the spindle, we further observed that the association of KMTs with non-KMTs predominantly occurs in the spindle pole regions. Our 3D reconstructions have implications for KMT growth and k-fiber self-organization models as covered in a parallel publication applying complementary live-cell imaging in combination with biophysical modeling (Conway et al., 2022). Finally, we also introduce a new visualization tool allowing an interactive display of our 3D spindle data that will serve as a resource for further structural studies on mitosis in human cells. eLife Sciences Publications, Ltd 2022-07-27 /pmc/articles/PMC9365394/ /pubmed/35894209 http://dx.doi.org/10.7554/eLife.75459 Text en © 2022, Kiewisz et al 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 Cell Biology
Kiewisz, Robert
Fabig, Gunar
Conway, William
Baum, Daniel
Needleman, Daniel
Müller-Reichert, Thomas
Three-dimensional structure of kinetochore-fibers in human mitotic spindles
title Three-dimensional structure of kinetochore-fibers in human mitotic spindles
title_full Three-dimensional structure of kinetochore-fibers in human mitotic spindles
title_fullStr Three-dimensional structure of kinetochore-fibers in human mitotic spindles
title_full_unstemmed Three-dimensional structure of kinetochore-fibers in human mitotic spindles
title_short Three-dimensional structure of kinetochore-fibers in human mitotic spindles
title_sort three-dimensional structure of kinetochore-fibers in human mitotic spindles
topic Cell Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9365394/
https://www.ncbi.nlm.nih.gov/pubmed/35894209
http://dx.doi.org/10.7554/eLife.75459
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