Cargando…
Loss of KLP-19 polar ejection force causes misorientation and missegregation of holocentric chromosomes
Holocentric chromosomes assemble kinetochores along their length instead of at a focused spot. The elongated expanse of an individual holocentric kinetochore and its potential flexibility heighten the risk of stable attachment to microtubules from both poles of the mitotic spindle (merotelic attachm...
Autores principales: | , , , , , |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
The Rockefeller University Press
2004
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1534123/ https://www.ncbi.nlm.nih.gov/pubmed/15452142 http://dx.doi.org/10.1083/jcb.200403036 |
_version_ | 1782129101733101568 |
---|---|
author | Powers, James Rose, Debra J. Saunders, Adam Dunkelbarger, Steven Strome, Susan Saxton, William M. |
author_facet | Powers, James Rose, Debra J. Saunders, Adam Dunkelbarger, Steven Strome, Susan Saxton, William M. |
author_sort | Powers, James |
collection | PubMed |
description | Holocentric chromosomes assemble kinetochores along their length instead of at a focused spot. The elongated expanse of an individual holocentric kinetochore and its potential flexibility heighten the risk of stable attachment to microtubules from both poles of the mitotic spindle (merotelic attachment), and hence aberrant segregation of chromosomes. Little is known about the mechanisms that holocentric species have evolved to avoid this type of error. Our studies of the influence of KLP-19, an essential microtubule motor, on the behavior of holocentric Caenorhabditis elegans chromosomes suggest that it has a major role in combating merotelic attachments. Depletion of KLP-19, which associates with nonkinetochore chromatin, allows aberrant poleward chromosome motion during prometaphase, misalignment of holocentric kinetochores, and multiple anaphase chromosome bridges in all mitotic divisions. Time-lapse movies of GFP-labeled mono- and bipolar spindles demonstrate that KLP-19 generates a force on relatively stiff holocentric chromosomes that pushes them away from poles. We hypothesize that this polar ejection force minimizes merotelic misattachment by maintaining a constant tension on pole–kinetochore connections throughout prometaphase, tension that compels sister kinetochores to face directly toward opposite poles. |
format | Text |
id | pubmed-1534123 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2004 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-15341232008-03-05 Loss of KLP-19 polar ejection force causes misorientation and missegregation of holocentric chromosomes Powers, James Rose, Debra J. Saunders, Adam Dunkelbarger, Steven Strome, Susan Saxton, William M. J Cell Biol Research Articles Holocentric chromosomes assemble kinetochores along their length instead of at a focused spot. The elongated expanse of an individual holocentric kinetochore and its potential flexibility heighten the risk of stable attachment to microtubules from both poles of the mitotic spindle (merotelic attachment), and hence aberrant segregation of chromosomes. Little is known about the mechanisms that holocentric species have evolved to avoid this type of error. Our studies of the influence of KLP-19, an essential microtubule motor, on the behavior of holocentric Caenorhabditis elegans chromosomes suggest that it has a major role in combating merotelic attachments. Depletion of KLP-19, which associates with nonkinetochore chromatin, allows aberrant poleward chromosome motion during prometaphase, misalignment of holocentric kinetochores, and multiple anaphase chromosome bridges in all mitotic divisions. Time-lapse movies of GFP-labeled mono- and bipolar spindles demonstrate that KLP-19 generates a force on relatively stiff holocentric chromosomes that pushes them away from poles. We hypothesize that this polar ejection force minimizes merotelic misattachment by maintaining a constant tension on pole–kinetochore connections throughout prometaphase, tension that compels sister kinetochores to face directly toward opposite poles. The Rockefeller University Press 2004-09-27 /pmc/articles/PMC1534123/ /pubmed/15452142 http://dx.doi.org/10.1083/jcb.200403036 Text en Copyright © 2004, The Rockefeller University Press This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/). |
spellingShingle | Research Articles Powers, James Rose, Debra J. Saunders, Adam Dunkelbarger, Steven Strome, Susan Saxton, William M. Loss of KLP-19 polar ejection force causes misorientation and missegregation of holocentric chromosomes |
title | Loss of KLP-19 polar ejection force causes misorientation and missegregation of holocentric chromosomes |
title_full | Loss of KLP-19 polar ejection force causes misorientation and missegregation of holocentric chromosomes |
title_fullStr | Loss of KLP-19 polar ejection force causes misorientation and missegregation of holocentric chromosomes |
title_full_unstemmed | Loss of KLP-19 polar ejection force causes misorientation and missegregation of holocentric chromosomes |
title_short | Loss of KLP-19 polar ejection force causes misorientation and missegregation of holocentric chromosomes |
title_sort | loss of klp-19 polar ejection force causes misorientation and missegregation of holocentric chromosomes |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1534123/ https://www.ncbi.nlm.nih.gov/pubmed/15452142 http://dx.doi.org/10.1083/jcb.200403036 |
work_keys_str_mv | AT powersjames lossofklp19polarejectionforcecausesmisorientationandmissegregationofholocentricchromosomes AT rosedebraj lossofklp19polarejectionforcecausesmisorientationandmissegregationofholocentricchromosomes AT saundersadam lossofklp19polarejectionforcecausesmisorientationandmissegregationofholocentricchromosomes AT dunkelbargersteven lossofklp19polarejectionforcecausesmisorientationandmissegregationofholocentricchromosomes AT stromesusan lossofklp19polarejectionforcecausesmisorientationandmissegregationofholocentricchromosomes AT saxtonwilliamm lossofklp19polarejectionforcecausesmisorientationandmissegregationofholocentricchromosomes |