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KIF18A's neck linker permits navigation of microtubule-bound obstacles within the mitotic spindle
KIF18A (kinesin-8) is required for mammalian mitotic chromosome alignment. KIF18A confines chromosome movement to the mitotic spindle equator by accumulating at the plus-ends of kinetochore microtubule bundles (K-fibers), where it functions to suppress K-fiber dynamics. It is not understood how the...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Life Science Alliance LLC
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6337737/ https://www.ncbi.nlm.nih.gov/pubmed/30655363 http://dx.doi.org/10.26508/lsa.201800169 |
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author | Malaby, Heidi LH Lessard, Dominique V Berger, Christopher L Stumpff, Jason |
author_facet | Malaby, Heidi LH Lessard, Dominique V Berger, Christopher L Stumpff, Jason |
author_sort | Malaby, Heidi LH |
collection | PubMed |
description | KIF18A (kinesin-8) is required for mammalian mitotic chromosome alignment. KIF18A confines chromosome movement to the mitotic spindle equator by accumulating at the plus-ends of kinetochore microtubule bundles (K-fibers), where it functions to suppress K-fiber dynamics. It is not understood how the motor accumulates at K-fiber plus-ends, a difficult feat requiring the motor to navigate protein dense microtubule tracks. Our data indicate that KIF18A's relatively long neck linker is required for the motor's accumulation at K-fiber plus-ends. Shorter neck linker (sNL) variants of KIF18A display a deficiency in accumulation at the ends of K-fibers at the center of the spindle. Depletion of K-fiber–binding proteins reduces the KIF18A sNL localization defect, whereas their overexpression reduces wild-type KIF18A's ability to accumulate on this same K-fiber subset. Furthermore, single-molecule assays indicate that KIF18A sNL motors are less proficient in navigating microtubules coated with microtubule-associated proteins. Taken together, these results support a model in which KIF18A's neck linker length permits efficient navigation of obstacles to reach K-fiber ends during mitosis. |
format | Online Article Text |
id | pubmed-6337737 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Life Science Alliance LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-63377372019-01-22 KIF18A's neck linker permits navigation of microtubule-bound obstacles within the mitotic spindle Malaby, Heidi LH Lessard, Dominique V Berger, Christopher L Stumpff, Jason Life Sci Alliance Research Articles KIF18A (kinesin-8) is required for mammalian mitotic chromosome alignment. KIF18A confines chromosome movement to the mitotic spindle equator by accumulating at the plus-ends of kinetochore microtubule bundles (K-fibers), where it functions to suppress K-fiber dynamics. It is not understood how the motor accumulates at K-fiber plus-ends, a difficult feat requiring the motor to navigate protein dense microtubule tracks. Our data indicate that KIF18A's relatively long neck linker is required for the motor's accumulation at K-fiber plus-ends. Shorter neck linker (sNL) variants of KIF18A display a deficiency in accumulation at the ends of K-fibers at the center of the spindle. Depletion of K-fiber–binding proteins reduces the KIF18A sNL localization defect, whereas their overexpression reduces wild-type KIF18A's ability to accumulate on this same K-fiber subset. Furthermore, single-molecule assays indicate that KIF18A sNL motors are less proficient in navigating microtubules coated with microtubule-associated proteins. Taken together, these results support a model in which KIF18A's neck linker length permits efficient navigation of obstacles to reach K-fiber ends during mitosis. Life Science Alliance LLC 2019-01-17 /pmc/articles/PMC6337737/ /pubmed/30655363 http://dx.doi.org/10.26508/lsa.201800169 Text en © 2019 Malaby et al. https://creativecommons.org/licenses/by/4.0/This article is available under a Creative Commons License (Attribution 4.0 International, as described at https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Research Articles Malaby, Heidi LH Lessard, Dominique V Berger, Christopher L Stumpff, Jason KIF18A's neck linker permits navigation of microtubule-bound obstacles within the mitotic spindle |
title | KIF18A's neck linker permits navigation of microtubule-bound obstacles within the mitotic spindle |
title_full | KIF18A's neck linker permits navigation of microtubule-bound obstacles within the mitotic spindle |
title_fullStr | KIF18A's neck linker permits navigation of microtubule-bound obstacles within the mitotic spindle |
title_full_unstemmed | KIF18A's neck linker permits navigation of microtubule-bound obstacles within the mitotic spindle |
title_short | KIF18A's neck linker permits navigation of microtubule-bound obstacles within the mitotic spindle |
title_sort | kif18a's neck linker permits navigation of microtubule-bound obstacles within the mitotic spindle |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6337737/ https://www.ncbi.nlm.nih.gov/pubmed/30655363 http://dx.doi.org/10.26508/lsa.201800169 |
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