Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Malaby, Heidi LH, Lessard, Dominique V, Berger, Christopher L, Stumpff, Jason
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Life Science Alliance LLC 2019
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
_version_ 1783388319355240448
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
work_keys_str_mv AT malabyheidilh kif18asnecklinkerpermitsnavigationofmicrotubuleboundobstacleswithinthemitoticspindle
AT lessarddominiquev kif18asnecklinkerpermitsnavigationofmicrotubuleboundobstacleswithinthemitoticspindle
AT bergerchristopherl kif18asnecklinkerpermitsnavigationofmicrotubuleboundobstacleswithinthemitoticspindle
AT stumpffjason kif18asnecklinkerpermitsnavigationofmicrotubuleboundobstacleswithinthemitoticspindle