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Functional states of kinetochores revealed by laser microsurgery and fluorescent speckle microscopy

The impact of mechanical forces on kinetochore motility was investigated using laser microsurgery to detach kinetochores with associated chromatin (K fragment) from meiotic chromosomes in spermatocytes from the crane fly Nephrotoma suturalis. In spermatocytes, elastic tethers connect telomeres of ho...

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Autores principales: LaFountain, James R., Cohan, Christopher S., Oldenbourg, Rudolf
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The American Society for Cell Biology 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3237623/
https://www.ncbi.nlm.nih.gov/pubmed/22031294
http://dx.doi.org/10.1091/mbc.E11-06-0494
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author LaFountain, James R.
Cohan, Christopher S.
Oldenbourg, Rudolf
author_facet LaFountain, James R.
Cohan, Christopher S.
Oldenbourg, Rudolf
author_sort LaFountain, James R.
collection PubMed
description The impact of mechanical forces on kinetochore motility was investigated using laser microsurgery to detach kinetochores with associated chromatin (K fragment) from meiotic chromosomes in spermatocytes from the crane fly Nephrotoma suturalis. In spermatocytes, elastic tethers connect telomeres of homologues during anaphase A of meiosis I, thus preventing complete disjunction until mid- to late anaphase A. K fragments liberated from tethered arms moved at twice the normal velocity toward their connected poles. To assess functional states of detached and control kinetochores, we loaded cells with fluorescently labeled tubulin for fluorescent speckle microscopy on kinetochore microtubules. Control kinetochores added fluorescent speckles at the kinetochore during anaphase A, whereas kinetochores of K fragments generally did not. In cases in which speckles reappeared in K-fragment K fibers, speckles and K fragments moved poleward at similar velocities. Thus detached kinetochores convert from their normal polymerization (reverse pac-man) state to a different state, in which polymerization is not evident. We suggest that the converted state is “park,” in which kinetochores are anchored to plus ends of kinetochore microtubules that shorten exclusively at their polar ends.
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spelling pubmed-32376232012-03-01 Functional states of kinetochores revealed by laser microsurgery and fluorescent speckle microscopy LaFountain, James R. Cohan, Christopher S. Oldenbourg, Rudolf Mol Biol Cell Articles The impact of mechanical forces on kinetochore motility was investigated using laser microsurgery to detach kinetochores with associated chromatin (K fragment) from meiotic chromosomes in spermatocytes from the crane fly Nephrotoma suturalis. In spermatocytes, elastic tethers connect telomeres of homologues during anaphase A of meiosis I, thus preventing complete disjunction until mid- to late anaphase A. K fragments liberated from tethered arms moved at twice the normal velocity toward their connected poles. To assess functional states of detached and control kinetochores, we loaded cells with fluorescently labeled tubulin for fluorescent speckle microscopy on kinetochore microtubules. Control kinetochores added fluorescent speckles at the kinetochore during anaphase A, whereas kinetochores of K fragments generally did not. In cases in which speckles reappeared in K-fragment K fibers, speckles and K fragments moved poleward at similar velocities. Thus detached kinetochores convert from their normal polymerization (reverse pac-man) state to a different state, in which polymerization is not evident. We suggest that the converted state is “park,” in which kinetochores are anchored to plus ends of kinetochore microtubules that shorten exclusively at their polar ends. The American Society for Cell Biology 2011-12-15 /pmc/articles/PMC3237623/ /pubmed/22031294 http://dx.doi.org/10.1091/mbc.E11-06-0494 Text en © 2011 LaFountain et al. This article is distributed by The American Society for Cell Biology under license from the author(s). Two months after publication it is available to the public under an Attribution–Noncommercial–Share Alike 3.0 Unported Creative Commons License (http://creativecommons.org/licenses/by-nc-sa/3.0). “ASCB®,” “The American Society for Cell Biology®,” and “Molecular Biology of the Cell®” are registered trademarks of The American Society of Cell Biology.
spellingShingle Articles
LaFountain, James R.
Cohan, Christopher S.
Oldenbourg, Rudolf
Functional states of kinetochores revealed by laser microsurgery and fluorescent speckle microscopy
title Functional states of kinetochores revealed by laser microsurgery and fluorescent speckle microscopy
title_full Functional states of kinetochores revealed by laser microsurgery and fluorescent speckle microscopy
title_fullStr Functional states of kinetochores revealed by laser microsurgery and fluorescent speckle microscopy
title_full_unstemmed Functional states of kinetochores revealed by laser microsurgery and fluorescent speckle microscopy
title_short Functional states of kinetochores revealed by laser microsurgery and fluorescent speckle microscopy
title_sort functional states of kinetochores revealed by laser microsurgery and fluorescent speckle microscopy
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3237623/
https://www.ncbi.nlm.nih.gov/pubmed/22031294
http://dx.doi.org/10.1091/mbc.E11-06-0494
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