Literature DB >> 1936559

Cortical morphogenesis in Paramecium: a transcellular wave of protein phosphorylation involved in ciliary rootlet disassembly.

L Sperling1, G Keryer, F Ruiz, J Beisson.   

Abstract

In Paramecium, the morphogenesis of the cortex at cell division, which assures reconstruction of shape and surface pattern, has been shown to involve transcellular signals which spread across the cortex like a wave, originating principally from the oral apparatus. One of the events these signals control is the reorganization of the ciliary rootlets through a cycle of regression and regrowth. The ciliary rootlets are nucleated on the ciliary basal bodies and form a scaffold extending over the entire cell surface that is important in aligning the basal bodies and the unit territories organized around them in longitudinal rows. We present evidence that the mechanism underlying their reorganization is cell-cycle-dependent phosphorylation of the structural proteins which compose the ciliary rootlets. We have isolated the rootlets and prepared a polyclonal antibody against them. In situ immunofluorescence of dividing cells with the anti rootlet antibody, and with the monoclonal antibody MPM-2 specific for phosphoproteins shows that a wave of phosphorylation of the ciliary rootlets spreads across the cell at division and just precedes their regression. Two-dimensional Western blot analysis of cytoskeleton and isolated rootlets along with alkaline phosphatase treatment demonstrates that the rootlets are composed of phosphoproteins, while experiments with interphase and dividing cells provide direct evidence that hyperphosphorylation of these proteins at division brings about disassembly of the structure.

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Year:  1991        PMID: 1936559     DOI: 10.1016/0012-1606(91)90330-6

Source DB:  PubMed          Journal:  Dev Biol        ISSN: 0012-1606            Impact factor:   3.582


  17 in total

1.  Bug22p, a conserved centrosomal/ciliary protein also present in higher plants, is required for an effective ciliary stroke in Paramecium.

Authors:  C Laligné; C Klotz; N Garreau de Loubresse; M Lemullois; M Hori; F X Laurent; J F Papon; B Louis; J Cohen; F Koll
Journal:  Eukaryot Cell       Date:  2010-01-29

2.  Homology-dependent gene silencing in Paramecium.

Authors:  F Ruiz; L Vayssié; C Klotz; L Sperling; L Madeddu
Journal:  Mol Biol Cell       Date:  1998-04       Impact factor: 4.138

3.  A large multigene family codes for the polypeptides of the crystalline trichocyst matrix in Paramecium.

Authors:  L Madeddu; M C Gautier; L Vayssié; A Houari; L Sperling
Journal:  Mol Biol Cell       Date:  1995-06       Impact factor: 4.138

4.  Characterization of multigene families in the micronuclear genome of Paramecium tetraurelia reveals a germline specific sequence in an intron of a centrin gene.

Authors:  L Vayssié; L Sperling; L Madeddu
Journal:  Nucleic Acids Res       Date:  1997-03-01       Impact factor: 16.971

5.  Molecular identification of a calcium-inhibited catalytic subunit of casein kinase type 2 from Paramecium tetraurelia.

Authors:  Daniel Vetter; Roland Kissmehl; Tilman Treptau; Karin Hauser; Josef Kellermann; Helmut Plattner
Journal:  Eukaryot Cell       Date:  2003-12

Review 6.  Choosing sides--asymmetric centriole and basal body assembly.

Authors:  Chad G Pearson
Journal:  J Cell Sci       Date:  2014-06-03       Impact factor: 5.285

7.  Proteins related to green algal striated fiber assemblin are present in stramenopiles and alveolates.

Authors:  John D I Harper; Jacques Thuet; Karl F Lechtreck; Adrienne R Hardham
Journal:  Protoplasma       Date:  2009-03-31       Impact factor: 3.356

8.  Evidence for defects in membrane traffic in Paramecium secretory mutants unable to produce functional storage granules.

Authors:  M C Gautier; N Garreau de Loubresse; L Madeddu; L Sperling
Journal:  J Cell Biol       Date:  1994-03       Impact factor: 10.539

9.  SF-assemblin, the structural protein of the 2-nm filaments from striated microtubule associated fibers of algal flagellar roots, forms a segmented coiled coil.

Authors:  K Weber; N Geisler; U Plessmann; A Bremerich; K F Lechtreck; M Melkonian
Journal:  J Cell Biol       Date:  1993-05       Impact factor: 10.539

10.  Major epiplasmic proteins of ciliates are articulins: cloning, recombinant expression, and structural characterization.

Authors:  I Huttenlauch; N Geisler; U Plessmann; R K Peck; K Weber; R Stick
Journal:  J Cell Biol       Date:  1995-09       Impact factor: 10.539

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