Mechanisms for focusing mitotic spindle poles by minus end–directed motor proteins
Open accessAbstract
During the formation of the metaphase spindle in animal somatic cells, kinetochore microtubule bundles (K fibers) are often disconnected from centrosomes, because they are released from centrosomes or directly generated from chromosomes. To create the tightly focused, diamond-shaped appearance of the bipolar spindle, K fibers need to be interconnected with centrosomal microtubules (C-MTs) by minus end–directed motor proteins. Here, we have characterized the roles of two minus end–directed motors, dynein and Ncd, in such processes in Drosophila S2 cells using RNA interference and high resolution microscopy. Even though these two motors have overlapping functions, we show that Ncd is primarily responsible for focusing K fibers, whereas dynein has a dominant function in transporting K fibers to the centrosomes. We also report a novel localization of Ncd to the growing tips of C-MTs, which we show is mediated by the plus end–tracking protein, EB1. Computer modeling of the K fiber focusing process suggests that the plus end localization of Ncd could facilitate the capture and transport of K fibers along C-MTs. From these results and simulations, we propose a model on how two minus end–directed motors cooperate to ensure spindle pole coalescence during mitosis.
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The second role of minus end-directed kinesins is to organize spindle MTs at MT minus ends and focus them into spindle poles.
“The second role is to organize spindle MTs at MT minus ends and focus them into spindle poles (5)(6)(7).”
From Diffusion and Directed Movement (2008) · cites this paper as [7]
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References 39 · Cited by 259
- Authors
- Goshima, G., Nédélec, F., & Vale, R. D.
- Affiliations
- Howard Hughes Medical Institute (US)
- 2The European Molecular Biology Laboratory, Cell Biology and Biophysics Programme, 69117 Heidelberg, Germany
- Corresponding author
- Goshima, Gohta
- Venue
- The Journal of Cell Biology
- Publisher
- Rockefeller University Press
- Published
- 2005-10-24
- Volume
- 171
- Issue
- 2
- Pages
- 229-240
- ISSN
- 0021-9525 (ISSN-L)
- 1540-8140
- PMC
- PMC2171195
- OpenAlex
- W2130217713
- Cited by
- 259
- References
- 39
- Citations by year
- 2026: 4 · 2025: 8 · 2024: 5 · 2023: 10 · 2022: 9 · 2021: 12 · 2020: 14 · 2019: 11 · 2018: 14 · 2017: 19 · 2016: 12 · 2015: 15 · 2014: 13 · 2013: 8 · 2012: 13
- FWCI
- 6.78
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Licence
- cc-by-nc-sa
- Locations
- The Journal of Cell Biology (publishedVersion)
- PubMed Central (publishedVersion, cc-by-nc-sa)
- PubMed (publishedVersion)
- eScholarship (California Digital Library) (submittedVersion)
- eScholarship (California Digital Library) (submittedVersion, cc-by-nc-sa)
- Funders
- National Institute of General Medical Sciences (R01GM038499)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Microtubule and mitosis dynamics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Genomics and Chromatin Dynamics
- Health Sciences › Medicine › Oncology › Cancer Treatment and Pharmacology
- Keywords
- mitotic spindle, kinetochore microtubules, dynein, EB1, microtubule transport, Drosophila S2 cells, metaphase spindle
- MeSH terms
- Animals, Cell Line, Computer Simulation, Drosophila, Dyneins, Microtubule-Associated Proteins, Microtubules, Mitosis, Spindle Apparatus, Phenotype, Kinesins, Centrosome, Drosophila Proteins, RNA Interference, Green Fluorescent Proteins
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