Axonal Growth Is Sensitive to the Levels of Katanin, a Protein That Severs Microtubules
Open accessAbstract
Katanin is a heterodimeric enzyme that severs microtubules from the centrosome so that they can move into the axon. Katanin is broadly distributed in the neuron, and therefore presumably also severs microtubules elsewhere. Such severing would generate multiple short microtubules from longer microtubules, resulting in more microtubule ends available for assembly and interaction with other structures. In addition, shorter microtubules are thought to move more rapidly and undergo organizational changes more readily than longer microtubules. In dividing cells, the levels of P60-katanin (the subunit with severing properties) increase as the cell transitions from interphase to mitosis. This suggests that katanin is regulated in part by its absolute levels, given that katanin activity is high during mitosis. In the rodent brain, neurons vary significantly in katanin levels, depending on their developmental stage. Levels are high during rapid phases of axonal growth but diminish as axons reach their targets. Similarly, in neuronal cultures, katanin levels are high when axons are allowed to grow avidly but drop when the axons are presented with target cells that cause them to stop growing. Expression of a dominant-negative P60-katanin construct in cultured neurons inhibits microtubule severing and is deleterious to axonal growth. Overexpression of wild-type P60-katanin results in excess microtubule severing and is also deleterious to axonal growth, but this only occurs in some neurons. Other neurons are relatively unaffected by overexpression. Collectively, these observations indicate that axonal growth is sensitive to the levels of P60-katanin, but that other factors contribute to modulating this sensitivity.
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Some microtubule-related genes associated with axonal transport and known to play a role in post-mitotic neural wiring and plasticity are associated with signals of positive selection, such as KIF18A or KATNA1.
“Some of the aforementioned microtubule-related genes, specifically those associated with axonal transport and known to play a role in post-mitotic neural wiring and plasticity93, are associated with signals of positive selection, such as KIF18A94 or KATNA195,96.”
From A catalog of single nucleotide changes distinguishing modern humans from archaic hominins (2019) · cites this paper as [96]
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Cites
Molecular Cloning: A Laboratory Manual
Sambrook, J., Fritsch, E., & Maniatis, T. (1989) · UCLA - Biblioteca de Ciencias de la Salud · Cited by 133,589 · see citing works
Ashburner, M. (1989) · Cold Spring Harbor Laboratory eBooks · Cited by 6,739 · see citing works
Banker, G. A., & Goslin, K. (1998) · Cited by 1,290 · see citing works
Identification of katanin, an ATPase that severs and disassembles stable microtubules
McNally, F. J., & Vale, R. D. (1993) · Cell · doi:10.1016/0092-8674(93)90377-3 · Cited by 517 · see citing works
Baas, P. W., & Black, M. M. (1990) · The Journal of cell biology · doi:10.1083/jcb.111.2.495 · Cited by 362 · see citing works
Self-citationHartman, J. J., Mahr, J., McNally, K. P., Okawa, K., Iwamatsu, A., Thomas, S. M., Cheesman, S., Heuser, J., Vale, R. D., & McNally, F. J. (1998) · Cell · doi:10.1016/s0092-8674(00)81578-0 · Cited by 344 · see citing works
Errico, A. (2002) · Human Molecular Genetics · doi:10.1093/hmg/11.2.153 · Cited by 340 · see citing works
Dynamic instability of microtubules is regulated by force
Janson, M. E., de Dood, M. E., & Dogterom, M. (2003) · The Journal of Cell Biology · doi:10.1083/jcb.200301147 · Cited by 287 · see citing works
Kinesin Superfamily Protein 2A (KIF2A) Functions in Suppression of Collateral Branch Extension
Homma, N., Takei, Y., Tanaka, Y., Nakata, T., Terada, S., Kikkawa, M., Noda, Y., & Hirokawa, N. (2003) · Cell · doi:10.1016/s0092-8674(03)00522-1 · Cited by 281 · see citing works
Dent, E. W., Callaway, J. L., Szebenyi, G., Baas, P. W., & Kalil, K. (1999) · Journal of Neuroscience · doi:10.1523/jneurosci.19-20-08894.1999 · Cited by 265 · see citing works
Self-citationAn Essential Role for Katanin in Severing Microtubules in the Neuron
Ahmad, F. J., Yu, W., McNally, F. J., & Baas, P. W. (1999) · The Journal of Cell Biology · doi:10.1083/jcb.145.2.305 · Cited by 253 · see citing works
Self-citationCytoplasmic Dynein and Dynactin Are Required for the Transport of Microtubules into the Axon
Ahmad, F. J., Echeverri, C. J., Vallee, R. B., & Baas, P. W. (1998) · The Journal of Cell Biology · doi:10.1083/jcb.140.2.391 · Cited by 216 · see citing works
Self-citationSevering of stable microtubules by a mitotically activated protein in xenopus egg extracts
Vale, R. D. (1991) · Cell · doi:10.1016/0092-8674(91)90511-v · Cited by 196 · see citing works
Rapid Movement of Microtubules in Axons
Wang, L., & Brown, A. (2002) · Current Biology · doi:10.1016/s0960-9822(02)01078-3 · Cited by 183 · see citing works
p75 Is Important for Axon Growth and Schwann Cell Migration during Development
Bentley, C. A., & Lee, K. (2000) · Journal of Neuroscience · doi:10.1523/jneurosci.20-20-07706.2000 · Cited by 181 · see citing works
Role of the microtubule destabilizing proteins SCG10 and stathmin in neuronal growth
Grenningloh, G., Brossard, S. S., Bondallaz, P., Ruchti, E., & Cadas, H. (2003) · Journal of Neurobiology · doi:10.1002/neu.10279 · Cited by 177 · see citing works
Motor proteins regulate force interactions between microtubules and microfilaments in the axon
Ahmad, F. J., Hughey, J., Wittmann, T., Hyman, A. A., Greaser, M. L., & Baas, P. W. (2000) · Nature Cell Biology · doi:10.1038/35010544 · Cited by 167 · see citing works
Self-citationAvila, J., Dominguez, J., & Díaz‐Nido, J. (1994) · The International Journal of Developmental Biology · doi:10.1387/ijdb.8074993 · Cited by 167 · see citing works
Cytoskeletal Plasticity in Cells Expressing Neuronal Microtubule-Associated Proteins
Kaech, S., Ludin, B., & Matus, A. I. (1996) · Neuron · doi:10.1016/s0896-6273(00)80249-4 · Cited by 163 · see citing works
Ebneth, A., Drewes, G., & Mandelkow, E. (1999) · Cell Motility and the Cytoskeleton · doi:10.1002/(sici)1097-0169(199911)44:3 · Cited by 161 · see citing works
Microtubule bending and breaking in living fibroblast cells
Odde, D. J., Ma, L., Briggs, A. H., DeMarco, A. L., & Kirschner, M. W. (1999) · Journal of Cell Science · doi:10.1242/jcs.112.19.3283 · Cited by 159 · see citing works
Two domains of p80 katanin regulate microtubule severing and spindle pole targeting by p60 katanin
Perry, K. L., Bazirgan, O. A., & McNally, F. J. (2000) · Journal of Cell Science · doi:10.1242/jcs.113.9.1623 · Cited by 156 · see citing works
Microtubule fragmentation and partitioning in the axon during collateral branch formation
Yu, W., Ahmad, F., & Baas, P. (1994) · Journal of Neuroscience · doi:10.1523/jneurosci.14-10-05872.1994 · Cited by 145 · see citing works
Self-citationMicrotubule nucleation and release from the neuronal centrosome
Yu, W., Centonze, V. E., Ahmad, F., & Baas, P. (1993) · The Journal of Cell Biology · doi:10.1083/jcb.122.2.349 · Cited by 132 · see citing works
Self-citationGamma-tubulin distribution in the neuron: implications for the origins of neuritic microtubules.
Baas, P. W., & Joshi, H. C. (1992) · The Journal of Cell Biology · doi:10.1083/jcb.119.1.171 · Cited by 119 · see citing works
Self-citationGupton, S. L., Salmon, W. C., & Waterman, C. M. (2002) · Current Biology · doi:10.1016/s0960-9822(02)01276-9 · Cited by 118 · see citing works
Slow axonal transport and the genesis of neuronal morphology
Baas, P. W., & Buster, D. W. (2003) · Journal of Neurobiology · doi:10.1002/neu.10281 · Cited by 97 · see citing works
Self-citationInhibition of microtubule nucleation at the neuronal centrosome compromises axon growth
Ahmad, F. J., Joshi, H. C., Centonze, V. E., & Baas, P. W. (1994) · Neuron · doi:10.1016/0896-6273(94)90270-4 · Cited by 95 · see citing works
Self-citationCerebellar target neurons provide a stop signal for afferent neurite extension in vitro
Baird, D., Hatten, M. E., & Mason, C. (1992) · Journal of Neuroscience · doi:10.1523/jneurosci.12-02-00619.1992 · Cited by 94 · see citing works
Self-citationA new perspective on microtubules and axon growth.
Joshi, H. C., & Baas, P. W. (1993) · The Journal of Cell Biology · doi:10.1083/jcb.121.6.1191 · Cited by 94 · see citing works
Self-citationThe Importance of Lattice Defects in Katanin-Mediated Microtubule Severing in Vitro
Davis, L. J., Odde, D. J., Block, S. M., & Gross, S. P. (2002) · Biophysical Journal · doi:10.1016/s0006-3495(02)75632-4 · Cited by 83 · see citing works
Microtubule Reconfiguration during Axonal Retraction Induced by Nitric Oxide
He, Y., Yu, W., & Baas, P. W. (2002) · Journal of Neuroscience · doi:10.1523/jneurosci.22-14-05982.2002 · Cited by 83 · see citing works
Self-citationKatanin‐mediated microtubule severing can be regulated by multiple mechanisms
Perry, K. L., Buster, D., & McNally, F. J. (2002) · Cell Motility and the Cytoskeleton · doi:10.1002/cm.10080 · Cited by 70 · see citing works
Roy, P. S., Petroll, W. M., Cavanagh, H. D., & Jester, J. V. (1999) · Cell Motility and the Cytoskeleton · doi:10.1002/(sici)1097-0169(1999)43:1 · Cited by 62 · see citing works
The Cerebellum: Purification and Coculture of Identified Cell Populations
Hatten, M. E., Gao, W., Morrison, M. E., et al. (1998) · The MIT Press eBooks · doi:10.7551/mitpress/4913.003.0023 · Cited by 29 · see citing works
Growing and Working with Peripheral Neurons
He, Y., & Baas, P. W. (2003) · Methods in cell biology · doi:10.1016/s0091-679x(03)01002-1 · Cited by 28 · see citing works
Self-citationSolowska, J. M., Mazurek, A. M., WEINBERGER, L., et al. (2002) · Molecular and Cellular Neuroscience · doi:10.1006/mcne.2002.1187 · Cited by 24 · see citing works
Self-citationDevelopmental Regulation of Mossy Fiber Afferent Interactions with Target Granule Cells
Zhang, Q., & Mason, C. A. (1998) · Developmental Biology · doi:10.1006/dbio.1997.8837 · Cited by 19 · see citing works
Micromethods for Analyzing Axon-Target Interactions in Vitro
Baird, D. H., Hatten, M. E., Heintz, N., et al. (1994) · Neuroprotocols · doi:10.1006/ncmn.1994.1013 · Cited by 10 · see citing works
Self-citation
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The Role of the Microtubule Cytoskeleton in Neurodevelopmental Disorders
Lasser, M., Tiber, J., & Lowery, L. A. (2018) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2018.00165 · Cited by 201 · see citing works
A catalog of single nucleotide changes distinguishing modern humans from archaic hominins
Kuhlwilm, M., & Boeckx, C. (2019) · Scientific Reports · doi:10.1038/s41598-019-44877-x · Cited by 108 · see citing works
- Authors
- Karabay, A., Yu, W., Solowska, J. M., Baird, D. H., & Baas, P. W.
- Affiliations
- Drexel University (US)
- Corresponding author
- Baas, Peter W.
- Venue
- The Journal of Neuroscience
- Publisher
- Society for Neuroscience
- Published
- 2004-06-23
- Volume
- 24
- Issue
- 25
- Pages
- 5778-5788
- ISSN
- 0270-6474 (ISSN-L)
- 1529-2401
- PMC
- PMC6729225
- OpenAlex
- W2103357770
- Cited by
- 147
- References
- 39
- Citations by year
- 2026: 3 · 2025: 2 · 2024: 3 · 2023: 2 · 2022: 8 · 2021: 9 · 2020: 8 · 2019: 11 · 2018: 13 · 2017: 1 · 2016: 8 · 2015: 4 · 2014: 8 · 2013: 9 · 2012: 12
- FWCI
- 2.11
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- Locations
- Journal of Neuroscience (publishedVersion, public-domain)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Istanbul Technical University Academic Open Archive (Istanbul Technical University) (submittedVersion)
- Funders
- National Institutes of Health
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Axon Guidance and Neuronal Signaling
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Microtubule and mitosis dynamics
- Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
- Keywords
- katanin, microtubule severing, axon growth, microtubules, centrosome, neuronal development, axon guidance, mitosis
- MeSH terms
- Katanin, Adenosine Triphosphatases, Amino Acid Sequence, Animals, Animals, Newborn, Axons, Brain, Cell Line, Fluorescent Antibody Technique, Humans, Microtubules, Molecular Sequence Data, Neurons, Sequence Homology, Amino Acid, In Situ Hybridization, Mice, Rats
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