Literature DB >> 16228902

Autonomous changes in the orientation of cortical microtubules underlying the helicoidal cell wall of the sunflower hypocotyl epidermis: spatial variation translated into temporal changes.

Z Hejnowicz1.   

Abstract

Angles (lambda) at which parallel cortical microtubules (cMTs) were oriented with respect to the longitudinal direction were measured in Helianthus annuus hypocotyl epidermal cells. Histograms showing lambda frequencies in cell populations at the instant of epidermis fixation were obtained. Analysis of the histograms indicates that, in a particular position within a cell, the angle lambda changes periodically with time, i.e., there is a cycle of lambda change at that position. This cycle is most likely rotational rather than oscillatory, i.e., the change in lambda has a defined chirality (clockwise or counterclockwise). The full diversity of histograms can be consistently explained by rotational cycles with a variable velocity of lambda change, and with a cMT rebuilding stage taking place at a different phase of the cycle. The rotational cycles also provide the simplest explanation of cMT arrays in which the angle lambda changes along a cell (fixed) and no parallel orientation of cMTs is apparent at a certain position. This explanation assumes a gradient in the phase of the rotational cycle along the cell. The symmetry of the angular characteristics of the rotational cycle, with respect to the morphological directions in cells, leads to the concept that these directions typically represent the principal directions of a certain tensor quantity, which may control the cycling. Possible interactions between the rotational cycle of cMT reorientation and the helicoidal cycle during cell wall formation are discussed.

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Year:  2005        PMID: 16228902     DOI: 10.1007/s00709-005-0091-9

Source DB:  PubMed          Journal:  Protoplasma        ISSN: 0033-183X            Impact factor:   3.356


  19 in total

1.  Gravity-induced reorientation of cortical microtubules observed in vivo.

Authors:  R Himmelspach; C L Wymer; C W Lloyd; P Nick
Journal:  Plant J       Date:  1999-05       Impact factor: 6.417

2.  A kinesin-like protein is essential for oriented deposition of cellulose microfibrils and cell wall strength.

Authors:  Ruiqin Zhong; David H Burk; W Herbert Morrison; Zheng-Hua Ye
Journal:  Plant Cell       Date:  2002-12       Impact factor: 11.277

3.  The cyclic reorientation of cortical microtubules in epidermal cells of azuki bean epicotyls: the role of actin filaments in the progression of the cycle.

Authors:  K Takesue; H Shibaoka
Journal:  Planta       Date:  1998-08       Impact factor: 4.116

Review 4.  Twisted liquid crystalline supramolecular arrangements in morphogenesis.

Authors:  M M Giraud-Guille
Journal:  Int Rev Cytol       Date:  1996

5.  Auxin Redistribution during First Positive Phototropism in Corn Coleoptiles : Microtubule Reorientation and the Cholodny-Went Theory.

Authors:  P Nick; E Schäfer; M Furuya
Journal:  Plant Physiol       Date:  1992-08       Impact factor: 8.340

6.  Dynamic microtubules under the radial and outer tangential walls of microinjected pea epidermal cells observed by computer reconstruction.

Authors:  M Yuan; R M Warn; P J Shaw; C W Lloyd
Journal:  Plant J       Date:  1995-01       Impact factor: 6.417

7.  Changes in microtubule arrays during the differentiation of cortical root cells of Raphanus sativus.

Authors:  J A Traas; P Braat; J W Derksen
Journal:  Eur J Cell Biol       Date:  1984-07       Impact factor: 4.492

8.  Extending the Microtubule/Microfibril paradigm. Cellulose synthesis is required for normal cortical microtubule alignment in elongating cells

Authors: 
Journal:  Plant Physiol       Date:  1998-03       Impact factor: 8.340

9.  A GFP-MAP4 reporter gene for visualizing cortical microtubule rearrangements in living epidermal cells

Authors: 
Journal:  Plant Cell       Date:  1998-11       Impact factor: 11.277

10.  Higher plant cortical microtubule array analyzed in vitro in the presence of the cell wall.

Authors:  Guo-Wei Tian; Damien Smith; Susanne Glück; Tobias I Baskin
Journal:  Cell Motil Cytoskeleton       Date:  2004-01
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  6 in total

1.  The tensor-based model for growth and cell divisions of the root apex. I. The significance of principal directions.

Authors:  Jerzy Nakielski
Journal:  Planta       Date:  2008-03-26       Impact factor: 4.116

2.  In Memoriam: Zygmunt Hejnowicz (1929-2016).

Authors:  Dorota Kwiatkowska; Jerzy Nakielski; Ewa U Kurczyńska
Journal:  Plant Signal Behav       Date:  2017-04-03

3.  Differential regulation of cellulose orientation at the inner and outer face of epidermal cells in the Arabidopsis hypocotyl.

Authors:  Elizabeth Faris Crowell; Hélène Timpano; Thierry Desprez; Tiny Franssen-Verheijen; Anne-Mie Emons; Herman Höfte; Samantha Vernhettes
Journal:  Plant Cell       Date:  2011-07-08       Impact factor: 11.277

4.  Arabidopsis cortical microtubules are initiated along, as well as branching from, existing microtubules.

Authors:  Jordi Chan; Adrian Sambade; Grant Calder; Clive Lloyd
Journal:  Plant Cell       Date:  2009-08-25       Impact factor: 11.277

5.  Generation of diverse biological forms through combinatorial interactions between tissue polarity and growth.

Authors:  Richard Kennaway; Enrico Coen; Amelia Green; Andrew Bangham
Journal:  PLoS Comput Biol       Date:  2011-06-16       Impact factor: 4.475

6.  A correlative microscopy approach relates microtubule behaviour, local organ geometry, and cell growth at the Arabidopsis shoot apical meristem.

Authors:  Agata Burian; Michal Ludynia; Magalie Uyttewaal; Jan Traas; Arezki Boudaoud; Olivier Hamant; Dorota Kwiatkowska
Journal:  J Exp Bot       Date:  2013-10-23       Impact factor: 6.992

  6 in total

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