spacer gif spacer gif spacer gif spacer gif spacer gif
 QUICK SEARCH:   [advanced]


spacer gif
     Home     Help     Feedback     Subscriptions     Archive     Search     Table of Contents    


This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Iftode, F
Right arrow Articles by Beisson, J
Right arrow Search for Related Content
PubMed
Right arrow Articles by Iftode, F
Right arrow Articles by Beisson, J
Social Bookmarking
 Add to CiteULike   Add to Complore   Add to Connotea   Add to Del.icio.us   Add to Digg   Add to Reddit   Add to Technorati   Add to Twitter  
What's this?
Development, Vol 105, Issue 2 191-211 Copyright © 1989 by Company of Biologists


Journal Articles

Development of surface pattern during division in Paramecium. I. Mapping of duplication and reorganization of cortical cytoskeletal structures in the wild type

F Iftode, J Cohen, F Ruiz, AT Rueda, L Chen-Shan, A Adoutte, and J Beisson

The shape of a Paramecium is determined by the organization of its cortex which constitutes most of the cell cytoskeleton. These structures and networks are organized in relation to the approx. 4000 ciliary basal bodies present at the surface. Each basal body is the centre of a polarized and asymmetrical cortical unit. At the whole-cell level, all units are tandemly arranged in parallel rows and form a defined asymmetrical pattern with dorsoventral and anteroposterior polarities. During division, the cortex is the site of the major morphogenetic processes. In order to analyse how the surface pattern and the shape of the cell are reconstructed at each division, we have used specific immunological and cytological probes to map, in space and time, the reorganization of each of the major cytoskeletal cortical components: basal bodies and microtubules, kinetodesmal fibres, epiplasm and outer lattice. This cytological dissection demonstrates that the surface of the dividing cell is progressively invaded by morphogenetic waves which successively and individually trigger the duplication, assembly or reorganization of each structure and which all spread from the same epicentre (oral apparatus and fission furrow) with the same shape. Furthermore, the response of units to the morphogenetic waves depends on their position on the cell. It thus appears that despite the structural local constraints within units, the development of surface pattern is controlled in an integrated manner by transcellular signals.
Add to CiteULike CiteULike   Add to Complore Complore   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us   Add to Digg Digg   Add to Reddit Reddit   Add to Technorati Technorati   Add to Twitter Twitter    What's this?


This article has been cited by other articles:


Home page
J. Cell Sci.Home page
I. M. Sehring, C. Reiner, J. Mansfeld, H. Plattner, and R. Kissmehl
A broad spectrum of actin paralogs in Paramecium tetraurelia cells display differential localization and function
J. Cell Sci., January 1, 2007; 120(1): 177 - 190.
[Abstract] [Full Text] [PDF]


Home page
Mol. Biol. CellHome page
R. Thazhath, M. Jerka-Dziadosz, J. Duan, D. Wloga, M. A. Gorovsky, J. Frankel, and J. Gaertig
Cell Context-specific Effects of the {beta}-Tubulin Glycylation Domain on Assembly and Size of Microtubular Organelles
Mol. Biol. Cell, September 1, 2004; 15(9): 4136 - 4147.
[Abstract] [Full Text] [PDF]


Home page
JCBHome page
P. Dupuis-Williams, A. Fleury-Aubusson, N. G. de Loubresse, H. Geoffroy, L. Vayssie, A. Galvani, A. Espigat, and J. Rossier
Functional role of {varepsilon}-tubulin in the assembly of the centriolar microtubule scaffold
J. Cell Biol., September 29, 2002; 158(7): 1183 - 1193.
[Abstract] [Full Text] [PDF]


Home page
J. Cell Sci.Home page
K. Kim, M. Son, J. B. Peterson, and D. L. Nelson
Ca2+-binding proteins of cilia and infraciliary lattice of Paramecium tetraurelia: their phosphorylation by purified endogenous Ca2+-dependent protein kinases
J. Cell Sci., January 5, 2002; 115(9): 1973 - 1984.
[Abstract] [Full Text] [PDF]


Home page
Mol. Biol. CellHome page
F. Ruiz, L. Vayssié, C. Klotz, L. Sperling, and L. Madeddu
Homology-dependent Gene Silencing in Paramecium
Mol. Biol. Cell, April 1, 1998; 9(4): 931 - 943.
[Abstract] [Full Text]


Home page
DevelopmentHome page
M Jerka-Dziadosz, F Ruiz, and F Beisson
Uncoupling of basal body duplication and cell division in crochu, a mutant of Paramecium hypersensitive to nocodazole
Development, January 4, 1998; 125(7): 1305 - 1314.
[Abstract] [PDF]


Home page
J. Cell Sci.Home page
M Prajer, A Fleury, and M Laurent
Dynamics of calcium regulation in Paramecium and possible morphogenetic implication
J. Cell Sci., January 3, 1997; 110(5): 529 - 535.
[Abstract] [PDF]


Home page
J. Cell Sci.Home page
N Levilliers, A Fleury, and A. Hill
Monoclonal and polyclonal antibodies detect a new type of post-translational modification of axonemal tubulin
J. Cell Sci., January 9, 1995; 108(9): 3013 - 3028.
[Abstract] [PDF]


Home page
J. Cell Sci.Home page
N Stelly, S Halpern, G Nicolas, P Fragu, and A Adoutte
Direct visualization of a vast cortical calcium compartment in Paramecium by secondary ion mass spectrometry (SIMS) microscopy: possible involvement in exocytosis
J. Cell Sci., January 5, 1995; 108(5): 1895 - 1909.
[Abstract] [PDF]




© The Company of Biologists Ltd 1989