Cited by 272Microtubule and mitosis dynamicsCancer Treatment and PharmacologyGenetic and Kidney Cyst Diseases

Enhanced stability of microtubules enriched in detyrosinated tubulin is not a direct function of detyrosination level

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Khawaja, S, Gundersen, G G, Bulinski, J C·1988·The Journal of cell biology

Abstract

Interphase cultured monkey kidney (TC-7) cells contain distinct subsets of cellular microtubules (MTs) enriched in posttranslationally detyrosinated (Glu) or tyrosinated (Tyr) alpha tubulin (Gundersen, G. G., M. H. Kalnoski, and J. C. Bulinski. 1984. Cell. 38:779-789). To determine the relative stability of these subsets of MTs, we subjected TC-7 cells to treatments that slowly depolymerized MTs. We found Glu MTs to be more resistant than Tyr MTs to depolymerization by nocodazole in living cells, and to depolymerization by dilution in detergent-permeabilized cell models. However, in cold-treated cells, Glu and Tyr MTs did not differ significantly in their stability. Digestion of permeabilized cell models with pancreatic carboxypeptidase A, to generate Glu MTs from endogenous Tyr MTs, did not significantly alter the resistance of the endogenous Tyr MTs toward dilution-induced depolymerization. Furthermore, in human fibroblasts that contained no distinct Glu MTs, we observed a population of nocodazole-resistant MTs. These data suggest that Glu MTs possess enhanced stability against end-mediated depolymerization, yet detyrosination alone appears to be insufficient to confer this enhanced stability.

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  • Increasing MT detyrosination by VSH1/SVBP overexpression does not confer stability to microtubules; the majority of detyrosinated MTs are lost upon nocodazole treatment.

    “we found that increasing MT detyrosination levels by overexpression of VSH1/SVBP does not confer stability to MTs as the majority of detyrosinated MTs were lost upon treatment with nocodazole (Fig. S1 G), in agreement with earlier work (Khawaja et al., 1988).”

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Authors
Khawaja, S., Gundersen, G. G., & Bulinski, J. C.
Affiliations
University of California, Los Angeles (US)
Venue
The Journal of cell biology
Published
1988-01-01
Volume
106
Issue
1
Pages
141-149
ISSN
  • 0021-9525 (ISSN-L)
  • 1540-8140
OpenAlex
W2116170706
Cited by
272
References
1
Citations by year
2026: 3 · 2025: 2 · 2024: 3 · 2023: 10 · 2022: 9 · 2021: 7 · 2020: 4 · 2019: 3 · 2018: 5 · 2017: 7 · 2016: 5 · 2015: 7 · 2014: 6 · 2013: 4 · 2012: 9
FWCI
7.95
Type
journal article
Language
en
Open access
Locations
  • The Journal of Cell Biology (publishedVersion)
  • PubMed Central (publishedVersion, cc-by-nc-sa)
  • PubMed (publishedVersion)
Funders
National Cancer Institute (CA39755)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Microtubule and mitosis dynamics
  • Health Sciences › Medicine › Oncology › Cancer Treatment and Pharmacology
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetic and Kidney Cyst Diseases
Keywords
microtubule stability, detyrosinated tubulin, alpha-tubulin, post-translational modification, nocodazole resistance, microtubule depolymerization, carboxypeptidase A, human fibroblasts, monkey kidney cells
MeSH terms
Animals, Benzimidazoles, Chlorocebus aethiops, Cold Temperature, Cytoskeleton, Fluorescent Antibody Technique, Glutamates, Microtubules, Polymers, Protein Binding, Solubility, Tubulin, Tyrosine, Nocodazole

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