Skip to main content
Plant Physiology logoLink to Plant Physiology
. 1997 Nov;115(3):1001–1007. doi: 10.1104/pp.115.3.1001

The characterization of plasma membrane-bound tubulin of cauliflower using Triton X-114 fractionation.

A Sonesson 1, M Berglund 1, I Staxén 1, S Widell 1
PMCID: PMC158563  PMID: 9390434

Abstract

The cortical microtubules determine how cellulose microfibrils are deposited in the plant cell wall and are thus important for the control of cell expansion. To understand how microtubules can control microfibril deposition, the components that link the microtubules to the plasma membrane (PM) of plant cells must be isolated. To obtain information on the properties of the tubulin-membrane associations, cauliflower (Brassica oleracea) PM was subjected to Triton X-114 fractionation, and the distribution of alpha- and beta-tubulin was analyzed using immunoblotting. Approximately one-half of the PM-associated tubulin was solubilized by Triton X-114 and 10 to 15% of both alpha- and beta-tubulin was recovered in the detergent phase (indicative of hydrophobic properties) and 30 to 40% was recovered in the aqueous phase. The hydrophobic tubulin could be released from the membrane by high pH extraction with preserved hydrophobicity. A large part of the PM-associated tubulin was found in the Triton-insoluble fraction. When this insoluble material was extracted a second time, a substantial amount of hydrophobic tubulin was released if the salt concentration was increased, suggesting that the hydrophobic tubulin was linked to a high-salt-sensitive protein aggregate that probably includes other components of the cytoskeleton. The hydrophobicity of a fraction of PM-associated tubulin could reflect a direct or indirect interaction of this tubulin with the lipid bilayer or with an integral membrane protein and may represent the anchoring of the cortical microtubules to the PM, a key element in the regulation of cell expansion.

Full Text

The Full Text of this article is available as a PDF (2.4 MB).

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Bearden J. C., Jr Quantitation of submicrogram quantities of protein by an improved protein-dye binding assay. Biochim Biophys Acta. 1978 Apr 26;533(2):525–529. doi: 10.1016/0005-2795(78)90398-7. [DOI] [PubMed] [Google Scholar]
  2. Beltramo D. M., Nuñez M., Alonso A. D., Barra H. S. The relationship of hydrophobic tubulin with membranes in neural tissue. Mol Cell Biochem. 1994 Dec 7;141(1):57–63. doi: 10.1007/BF00935591. [DOI] [PubMed] [Google Scholar]
  3. Blancaflor E. B., Hasenstein K. H. Organization of cortical microtubules in graviresponding maize roots. Planta. 1993;191:231–237. doi: 10.1007/BF00199754. [DOI] [PubMed] [Google Scholar]
  4. Bordier C. Phase separation of integral membrane proteins in Triton X-114 solution. J Biol Chem. 1981 Feb 25;256(4):1604–1607. [PubMed] [Google Scholar]
  5. Chang-Jie J., Sonobe S. Identification and preliminary characterization of a 65 kDa higher-plant microtubule-associated protein. J Cell Sci. 1993 Aug;105(Pt 4):891–901. doi: 10.1242/jcs.105.4.891. [DOI] [PubMed] [Google Scholar]
  6. Cox D. N., Muday G. K. NPA binding activity is peripheral to the plasma membrane and is associated with the cytoskeleton. Plant Cell. 1994 Dec;6(12):1941–1953. doi: 10.1105/tpc.6.12.1941. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Cyr R. J., Palevitz B. A. Organization of cortical microtubules in plant cells. Curr Opin Cell Biol. 1995 Feb;7(1):65–71. doi: 10.1016/0955-0674(95)80046-8. [DOI] [PubMed] [Google Scholar]
  8. Durso N. A., Cyr R. J. A calmodulin-sensitive interaction between microtubules and a higher plant homolog of elongation factor-1 alpha. Plant Cell. 1994 Jun;6(6):893–905. doi: 10.1105/tpc.6.6.893. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Hardham A. R., Gunning B. E. Structure of cortical microtubule arrays in plant cells. J Cell Biol. 1978 Apr;77(1):14–34. doi: 10.1083/jcb.77.1.14. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Johansson F., Olbe M., Sommarin M., Larsson C. Brij 58, a polyoxyethylene acyl ether, creates membrane vesicles of uniform sidedness. A new tool to obtain inside-out (cytoplasmic side-out) plasma membrane vesicles. Plant J. 1995 Jan;7(1):165–173. doi: 10.1046/j.1365-313x.1995.07010165.x. [DOI] [PubMed] [Google Scholar]
  11. Johansson I., Larsson C., Ek B., Kjellbom P. The major integral proteins of spinach leaf plasma membranes are putative aquaporins and are phosphorylated in response to Ca2+ and apoplastic water potential. Plant Cell. 1996 Jul;8(7):1181–1191. doi: 10.1105/tpc.8.7.1181. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Laemmli U. K. Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature. 1970 Aug 15;227(5259):680–685. doi: 10.1038/227680a0. [DOI] [PubMed] [Google Scholar]
  13. Lambert A. M. Microtubule-organizing centers in higher plants. Curr Opin Cell Biol. 1993 Feb;5(1):116–122. doi: 10.1016/s0955-0674(05)80016-x. [DOI] [PubMed] [Google Scholar]
  14. Liu B., Joshi H. C., Wilson T. J., Silflow C. D., Palevitz B. A., Snustad D. P. gamma-Tubulin in Arabidopsis: gene sequence, immunoblot, and immunofluorescence studies. Plant Cell. 1994 Feb;6(2):303–314. doi: 10.1105/tpc.6.2.303. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Marc J., Sharkey D. E., Durso N. A., Zhang M., Cyr R. J. Isolation of a 90-kD Microtubule-Associated Protein from Tobacco Membranes. Plant Cell. 1996 Nov;8(11):2127–2138. doi: 10.1105/tpc.8.11.2127. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Nick P., Bergfeld R., Schafer E., Schopfer P. Unilateral reorientation of microtubules at the outer epidermal wall during photo- and gravitropic curvature of maize coleoptiles and sunflower hypocotyls. Planta. 1990 May;181(2):162–168. doi: 10.1007/BF02411533. [DOI] [PubMed] [Google Scholar]
  17. Nick P., Lambert A. M., Vantard M. A microtubule-associated protein in maize is expressed during phytochrome-induced cell elongation. Plant J. 1995 Dec;8(6):835–844. doi: 10.1046/j.1365-313x.1995.8060835.x. [DOI] [PubMed] [Google Scholar]
  18. Roa M., Cornet V., Yang C. Z., Goud B. The small GTP-binding protein rab6p is redistributed in the cytosol by brefeldin A. J Cell Sci. 1993 Nov;106(Pt 3):789–802. doi: 10.1242/jcs.106.3.789. [DOI] [PubMed] [Google Scholar]
  19. Skene J. H., Virág I. Posttranslational membrane attachment and dynamic fatty acylation of a neuronal growth cone protein, GAP-43. J Cell Biol. 1989 Feb;108(2):613–624. doi: 10.1083/jcb.108.2.613. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. Thion L., Mazars C., Thuleau P., Graziana A., Rossignol M., Moreau M., Ranjeva R. Activation of plasma membrane voltage-dependent calcium-permeable channels by disruption of microtubules in carrot cells. FEBS Lett. 1996 Sep 9;393(1):13–18. doi: 10.1016/0014-5793(96)00844-7. [DOI] [PubMed] [Google Scholar]
  21. Vantard M., Schellenbaum P., Fellous A., Lambert A. M. Characterization of maize microtubule-associated proteins, one of which is immunologically related to tau. Biochemistry. 1991 Sep 24;30(38):9334–9340. doi: 10.1021/bi00102a028. [DOI] [PubMed] [Google Scholar]

Articles from Plant Physiology are provided here courtesy of Oxford University Press

RESOURCES