Journal
ELIFE
Volume 11, Issue -, Pages -Publisher
eLIFE SCIENCES PUBL LTD
DOI: 10.7554/eLife.75459
Keywords
spindle; kinetochore-microtubules; mitosis; k-fiber; 3D reconstruction; electron tomography; Human
Categories
Funding
- Deutsche Forschungsgemeinschaft [MU 1423/8-2, 675737, 1764269]
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In this study, the three-dimensional structure of kinetochore fibers in mammalian cells was characterized using large-scale electron tomography. It was found that each kinetochore fiber is composed of approximately nine kinetochore microtubules, with variations in circumference and density along their length. The association between kinetochore microtubules and non-kinetochore microtubules was primarily observed in the spindle pole regions.
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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