Cited by 147Axon Guidance and Neuronal SignalingMicrotubule and mitosis dynamicsNeurogenesis and neuroplasticity mechanisms

Axonal Growth Is Sensitive to the Levels of Katanin, a Protein That Severs Microtubules

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Karabay, Arzu, Yu, Wenqian, Solowska, Joanna M., Baird, Douglas H., Baas, Peter W.·2004·The Journal of Neuroscience

Abstract

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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Crossref · 10.1523/jneurosci.1382-04.2004

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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.”

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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
Published
2004-06-23
Volume
24
Issue
25
Pages
5778-5788
ISSN
  • 0270-6474 (ISSN-L)
  • 1529-2401
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
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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