Literature DB >> 11607479

Dynamic reorientation of cortical microtubules, from transverse to longitudinal, in living plant cells.

M Yuan1, P J Shaw, R M Warn, C W Lloyd.   

Abstract

The direction in which plant tissue cells expand is reflected in the alignment of microtubules in the cortical array. When microtubules and coaligned wall microfibrils are arranged transversely around the cell, turgor pressure is chaneled into cell elongation. However, various agents (such as wounding, ethylene, abscisic acid) can cause the microtubules to reorientate by 90 degrees so that they become aligned parallel to the cell's long axis, allowing lateral expansion instead of elongation. The mechanism by which microtubules undergo rapid shifts of alignment is crucial to understanding growth control in plants, but because current models are derived from studies on fixed cells, nothing is known about the dynamics of converting one microtubule alignment to another. Cells tend to have one predominant microtubule alignment--transverse, oblique, or longitudinal--but it is not established whether each represents a stable independent set that only changes by rounds of complete de- and repolymerization, or whether reorientation is a more continuous process involving movement of stable or dynamic microtubules. By microinjecting pea (Pisum sativum) epidermal cells with rhodamine-conjugated brain tubulin and optically sectioning them by confocal laser scanning microscopy, we could follow labeled microtubules for up to 2 hr as they reorientate. Reorientation does not occur by complete depolymerization of microtubules in one orientation followed by polymerization of a new array in another orientation. Instead, increased numbers of discordant microtubules in nontransverse alignment appear in particular locations. Neighboring microtubules then adopt the new alignment, so that there is a stage during which different alignments coexist before the array on the outer tangential cell face finally adopts a uniform steeply oblique/longitudinal configuration. Rapid fluorescence recovery after photobleaching confirms that bundles of cortical microtubules are not stable but exhibit properties consistent with dynamic instability. Dynamic microtubules offer a mechanism for rapid growth responses to a range of physiological stimuli.

Entities:  

Year:  1994        PMID: 11607479      PMCID: PMC44135          DOI: 10.1073/pnas.91.13.6050

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


  8 in total

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Authors:  D Zhang; P Wadsworth; P K Hepler
Journal:  Proc Natl Acad Sci U S A       Date:  1990-11       Impact factor: 11.205

2.  Preparation of modified tubulins.

Authors:  A Hyman; D Drechsel; D Kellogg; S Salser; K Sawin; P Steffen; L Wordeman; T Mitchison
Journal:  Methods Enzymol       Date:  1991       Impact factor: 1.600

3.  Association of high-molecular-weight proteins with microtubules and their role in microtubule assembly in vitro.

Authors:  D B Murphy; G G Borisy
Journal:  Proc Natl Acad Sci U S A       Date:  1975-07       Impact factor: 11.205

4.  Dynamic instability of microtubule growth.

Authors:  T Mitchison; M Kirschner
Journal:  Nature       Date:  1984 Nov 15-21       Impact factor: 49.962

5.  Activities of dipeptidyl peptidase II and dipeptidyl peptidase IV in synovial fluid from patients with rheumatoid arthritis and osteoarthritis.

Authors:  H Gotoh; M Hagihara; T Nagatsu; H Iwata; T Miura
Journal:  Clin Chem       Date:  1989-06       Impact factor: 8.327

6.  Amino acid sequence requirements in the epitope recognized by the alpha-tubulin-specific rat monoclonal antibody YL 1/2.

Authors:  J Wehland; H C Schröder; K Weber
Journal:  EMBO J       Date:  1984-06       Impact factor: 11.598

7.  Postpolymerization detyrosination of alpha-tubulin: a mechanism for subcellular differentiation of microtubules.

Authors:  G G Gundersen; S Khawaja; J C Bulinski
Journal:  J Cell Biol       Date:  1987-07       Impact factor: 10.539

8.  A rat monoclonal antibody reacting specifically with the tyrosylated form of alpha-tubulin. I. Biochemical characterization, effects on microtubule polymerization in vitro, and microtubule polymerization and organization in vivo.

Authors:  J Wehland; M C Willingham; I V Sandoval
Journal:  J Cell Biol       Date:  1983-11       Impact factor: 10.539

  8 in total
  53 in total

1.  The 65-kDa carrot microtubule-associated protein forms regularly arranged filamentous cross-bridges between microtubules.

Authors:  J Chan; C G Jensen; L C Jensen; M Bush; C W Lloyd
Journal:  Proc Natl Acad Sci U S A       Date:  1999-12-21       Impact factor: 11.205

Review 2.  Cell cycle regulation of the microtubular cytoskeleton.

Authors:  M Vantard; R Cowling; C Delichère
Journal:  Plant Mol Biol       Date:  2000-08       Impact factor: 4.076

3.  Identification of a novel plant-specific kinesin-like protein that is highly expressed in interphase tobacco BY-2 cells.

Authors:  K Matsui; D Collings; T Asada
Journal:  Protoplasma       Date:  2001       Impact factor: 3.356

Review 4.  The plant cytoskeleton: recent advances in the study of the plant microtubule-associated proteins MAP-65, MAP-190 and the Xenopus MAP215-like protein, MOR1.

Authors:  Patrick J Hussey; Timothy J Hawkins; Hisako Igarashi; Despina Kaloriti; Andrei Smertenko
Journal:  Plant Mol Biol       Date:  2002-12       Impact factor: 4.076

Review 5.  Helical microtubule arrays and spiral growth.

Authors:  Clive Lloyd; Jordi Chan
Journal:  Plant Cell       Date:  2002-10       Impact factor: 11.277

6.  Behavior of Microtubules in Living Plant Cells.

Authors:  P. K. Hepler; J. M. Hush
Journal:  Plant Physiol       Date:  1996-10       Impact factor: 8.340

7.  The cortical microtubule array: from dynamics to organization.

Authors:  Ram Dixit; Richard Cyr
Journal:  Plant Cell       Date:  2004-10       Impact factor: 11.277

8.  Large-scale vortex lattice emerging from collectively moving microtubules.

Authors:  Yutaka Sumino; Ken H Nagai; Yuji Shitaka; Dan Tanaka; Kenichi Yoshikawa; Hugues Chaté; Kazuhiro Oiwa
Journal:  Nature       Date:  2012-03-21       Impact factor: 49.962

9.  Understanding phase behavior of plant cell cortex microtubule organization.

Authors:  Xia-qing Shi; Yu-qiang Ma
Journal:  Proc Natl Acad Sci U S A       Date:  2010-06-14       Impact factor: 11.205

10.  SPIRAL1 encodes a plant-specific microtubule-localized protein required for directional control of rapidly expanding Arabidopsis cells.

Authors:  Keiji Nakajima; Ikuyo Furutani; Hideki Tachimoto; Hiroshige Matsubara; Takashi Hashimoto
Journal:  Plant Cell       Date:  2004-04-14       Impact factor: 11.277

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