|
|
|
||||
| Home Help Feedback Subscriptions Archive Search Table of Contents | |||||
Journal of Cell Science, Vol 92, Issue 1 57-65, Copyright © 1989 by Company of Biologists
JOURNAL ARTICLES |
DR Webster and GG Borisy
Laboratory of Molecular Biology, University of Wisconsin, Madison 53706.
Tubulin is subject to a post-translational acetylation reaction that is thought to be correlated with increased stability of the modified microtubules (MTs). We sought to test directly the stability of acetylated MTs by determining their specific rate of turnover. We used human fibroblasts, which contain a subset of MTs that display terminal and internal domains of acetylation. The turnover of acetylated domains was analysed by microinjecting cells with biotinylated brain tubulin and determining, by triple-label immunofluorescence, the progress of incorporation of biotinylated tubulin into acetylated and non-acetylated domains. Within two minutes after injection, biotinylated domains were contiguous with virtually all observed non-acetylated MT ends but were not contiguous with terminal acetylated domains, demonstrating that the former were growing while the latter were not. Ten minutes after injection, many MTs lacking acetylated domains had incorporated biotinylated subunits uniformly while most MTs containing acetylated domains remained unlabelled, indicating that non-acetylated MTs were turning over while most acetylated domains were not. One hour after injection, virtually all non-acetylated MTs were labelled with biotin whereas approximately half of the acetylated domains contained biotin, demonstrating that acetylated domains turned over much more slowly than the non-acetylated, bulk array. Non-acetylated MT regions flanking acetylated domains also lacked hapten, indicating that acetylation modified discrete regions along stable MTs. Sixteen hours after injection, cells that had not entered mitosis still retained acetylated domains that had not turned over (13% of all acetylated domains), indicating that acetylated domains can be extremely long-lived.(ABSTRACT TRUNCATED AT 250 WORDS)
This article has been cited by other articles:
![]() |
A. R. Barr and F. Gergely MCAK-Independent Functions of ch-Tog/XMAP215 in Microtubule Plus-End Dynamics Mol. Cell. Biol., December 1, 2008; 28(23): 7199 - 7211. [Abstract] [Full Text] [PDF] |
||||
![]() |
O. Azarenko, T. Okouneva, K. W. Singletary, M. A. Jordan, and L. Wilson Suppression of microtubule dynamic instability and turnover in MCF7 breast cancer cells by sulforaphane Carcinogenesis, December 1, 2008; 29(12): 2360 - 2368. [Abstract] [Full Text] [PDF] |
||||
![]() |
K. Kroboth, I. P. Newton, K. Kita, D. Dikovskaya, J. Zumbrunn, C. M. Waterman-Storer, and I. S. Nathke Lack of Adenomatous Polyposis Coli Protein Correlates with a Decrease in Cell Migration and Overall Changes in Microtubule Stability Mol. Biol. Cell, March 1, 2007; 18(3): 910 - 918. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. Hari, F. Loganzo, T. Annable, X. Tan, S. Musto, D. B. Morilla, J. H. Nettles, J. P. Snyder, and L. M. Greenberger Paclitaxel-resistant cells have a mutation in the paclitaxel-binding region of {beta}-tubulin (Asp26Glu) and less stable microtubules. Mol. Cancer Ther., February 1, 2006; 5(2): 270 - 278. [Abstract] [Full Text] [PDF] |
||||
![]() |
D. C. H. Ng, B. H. Lin, C. P. Lim, G. Huang, T. Zhang, V. Poli, and X. Cao Stat3 regulates microtubules by antagonizing the depolymerization activity of stathmin J. Cell Biol., January 17, 2006; 172(2): 245 - 257. [Abstract] [Full Text] [PDF] |
||||
![]() |
H. P. Cho, Y. Liu, M. Gomez, J. Dunlap, M. Tyers, and Y. Wang The Dual-Specificity Phosphatase CDC14B Bundles and Stabilizes Microtubules Mol. Cell. Biol., June 1, 2005; 25(11): 4541 - 4551. [Abstract] [Full Text] [PDF] |
||||
![]() |
C. Bouquet, S. Soares, Y. von Boxberg, M. Ravaille-Veron, F. Propst, and F. Nothias Microtubule-Associated Protein 1B Controls Directionality of Growth Cone Migration and Axonal Branching in Regeneration of Adult Dorsal Root Ganglia Neurons J. Neurosci., August 11, 2004; 24(32): 7204 - 7213. [Abstract] [Full Text] [PDF] |
||||
![]() |
C. M. Franz and A. J. Ridley p120 Catenin Associates with Microtubules: INVERSE RELATIONSHIP BETWEEN MICROTUBULE BINDING AND RHO GTPase REGULATION J. Biol. Chem., February 20, 2004; 279(8): 6588 - 6594. [Abstract] [Full Text] [PDF] |
||||
![]() |
C.M.H. Combelles, N.A. Cekleniak, C. Racowsky, and D.F. Albertini Assessment of nuclear and cytoplasmic maturation in in-vitro matured human oocytes Hum. Reprod., April 1, 2002; 17(4): 1006 - 1016. [Abstract] [Full Text] [PDF] |
||||
![]() |
L. Haren and A. Merdes Direct binding of NuMA to tubulin is mediated by a novel sequence motif in the tail domain that bundles and stabilizes microtubules J. Cell Sci., January 5, 2002; 115(9): 1815 - 1824. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. Can and O. Semiz Diethylstilbestrol (DES)-induced cell cycle delay and meiotic spindle disruption in mouse oocytes during in-vitro maturation Mol. Hum. Reprod., February 1, 2000; 6(2): 154 - 162. [Abstract] [Full Text] [PDF] |
||||
![]() |
D. Horesh, T. Sapir, F. Francis, S. G. Wolf, M. Caspi, M. Elbaum, J. Chelly, and O. Reiner Doublecortin, a stabilizer of microtubules Hum. Mol. Genet., September 1, 1999; 8(9): 1599 - 1610. [Abstract] [Full Text] [PDF] |
||||
![]() |
K Million, J Larcher, J Laoukili, D Bourguignon, F Marano, and F Tournier Polyglutamylation and polyglycylation of alpha- and beta-tubulins during in vitro ciliated cell differentiation of human respiratory epithelial cells J. Cell Sci., January 12, 1999; 112(23): 4357 - 4366. [Abstract] [PDF] |
||||
![]() |
C. Pous, K. Chabin, A. Drechou, L. Barbot, T. Phung-Koskas, C. Settegrana, M.L. Bourguet-Kondracki, M. Maurice, D. Cassio, M. Guyot, et al. Functional Specialization of Stable and Dynamic Microtubules in Protein Traffic in WIF-B Cells J. Cell Biol., July 13, 1998; 142(1): 153 - 165. [Abstract] [Full Text] [PDF] |
||||
![]() |
B. Cha, B Error, and D. Gard XMAP230 is required for the assembly and organization of acetylated microtubules and spindles in Xenopus oocytes and eggs J. Cell Sci., January 8, 1998; 111(16): 2315 - 2327. [Abstract] [PDF] |
||||
![]() |
A. Yvon and P Wadsworth Non-centrosomal microtubule formation and measurement of minus end microtubule dynamics in A498 cells J. Cell Sci., January 10, 1997; 110(19): 2391 - 2401. [Abstract] [PDF] |
||||
![]() |
M Laurent and A Fleury Hysteretic behavior and differential apparent stability properties of microtubule species emerge from the regulation of post-translational modifications of microtubules J. Cell Sci., January 2, 1996; 109(2): 419 - 428. [Abstract] [PDF] |
||||
![]() |
K. Wolf and H. Joshi Microtubule organization and the distribution of gamma-tubulin in spermatogenesis of a beetle, Tenebrio molitor (Tenebrionidae, Coleoptera, Insecta) J. Cell Sci., January 12, 1995; 108(12): 3855 - 3865. [Abstract] [PDF] |
||||
![]() |
R. Burns Analysis of the gamma-tubulin sequences: implications for the functional properties of gamma-tubulin J. Cell Sci., January 6, 1995; 108(6): 2123 - 2130. [PDF] |
||||
![]() |
J. Leger, R Brandt, and G Lee Identification of tau protein regions required for process formation in PC12 cells J. Cell Sci., January 12, 1994; 107(12): 3403 - 3412. [Abstract] [PDF] |
||||
![]() |
C Oakley and D. Brunette The sequence of alignment of microtubules, focal contacts and actin filaments in fibroblasts spreading on smooth and grooved titanium substrata J. Cell Sci., January 9, 1993; 106(1): 343 - 354. [Abstract] [PDF] |
||||