Book of Abstracts - Geyseco
Book of Abstracts - Geyseco
Book of Abstracts - Geyseco
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FESPB 2010 - XVII Congress <strong>of</strong> the Federation <strong>of</strong> European Societies <strong>of</strong> Plant Biology<br />
1<br />
Institut de Recherche en Biologie Végétale - Université de Montréal<br />
2<br />
Ecole Polytechnique de Montréal<br />
*Corresponding author, e-mail: youssef.chebli@yahoo.ca<br />
Cellular growth in plant cells is driven by the turgor pressure but<br />
controlled by the mechanical properties <strong>of</strong> the cell wall. The formation<br />
<strong>of</strong> a cellular protuberance requires the spatially confined<br />
yielding <strong>of</strong> the wall. Using finite element modeling, a technique<br />
used in engineering, we established a theoretical model <strong>of</strong> tip<br />
growth as it occurs in pollen tubes and root hairs.<br />
The model predicts that a characteristic spatial distribution <strong>of</strong><br />
mechanical properties in the cell wall is required to produce the<br />
self-similar growth pattern that characterizes these cell types.<br />
The mechanical pr<strong>of</strong>ile is characterized by a steep increase in cell<br />
wall extensibility in the transition zone between dome-shaped<br />
apex and cylindrical region <strong>of</strong> the cell.<br />
To compare the theoretical requirements with the biological<br />
reality, we quantitatively assessed the spatial distribution <strong>of</strong> various<br />
cell wall components in the pollen tube wall <strong>of</strong> Lilium and<br />
Arabidopsis. We used immun<strong>of</strong>luorescence methods combined<br />
with quantitative image analysis to locate pectin, cellulose and<br />
callose. We found remarkable agreement between the expected<br />
gradient in cell wall extensibility and the distribution <strong>of</strong> de-esterified<br />
pectin polymers. Furthermore, we identified the orientation<br />
<strong>of</strong> cellulose micr<strong>of</strong>ibrils using scanning electron microscopy and<br />
found that their mechanical support is particularly important in<br />
the transition region. Callose on the other hand provides mechanical<br />
support to the cylindrical shank <strong>of</strong> the cell. Our data show<br />
that tip growth is produced by a highly controlled interplay <strong>of</strong><br />
cell wall assembly processes and that each component is important<br />
for different aspects governing the shape and growth dynamics<br />
<strong>of</strong> the elongating cell.<br />
P11-014: KUNITZ TRYPSIN INHIBITOR AS A PLANT<br />
CELL DEATH MODULATOR<br />
Komarova, T.* - Sheval, E. - Dorokhov, Y.<br />
Moscow State University, A.N.Belozersky Institute<br />
*Corresponding author, e-mail: t.v.komarova@gmail.com<br />
Normally plant cell is adapted for producing large amounts <strong>of</strong><br />
protein which is targeted and stored in special cellular compartments.<br />
But intensive uncontrolled and untargeted protein<br />
production is likely to result in programmed cell death (PCD). To<br />
study cell death <strong>of</strong> protein overexpressing plant cell we created<br />
specific vector system, TMV:GFP, allowing GFP production in<br />
huge amounts and resulted in cells death 3 days after agroinjection.<br />
Using microscopy and biochemical approaches we described<br />
the following features <strong>of</strong> the process: stages <strong>of</strong> cell and tissue<br />
death; GFP behavior in aggregates and its proper folding. Moreover<br />
we analyzed the pattern <strong>of</strong> mRNA expression in Nicotiana<br />
benthamiana tissues just before their death using subtractive hybridization.<br />
Several candidate genes including specific biotic cell<br />
death-associated protein (CDM) were found to be upregulated.<br />
NbCDM appeared to have strong homology with Kunitz trypsin<br />
inhibitors (KTI) family which is specific for serine proteases<br />
been implicated in PCD in plants. Joint expression <strong>of</strong> NbCDM<br />
under control <strong>of</strong> 35S promoter (35S-NbCDM) with TMV:GFP<br />
resulted in enhanced lesion development whereas 35S-NbCDM<br />
per se didn’t induce necrotisation. Upregulation <strong>of</strong> NbCDM expression<br />
was also registered as a response to virulent bacterial pathogen<br />
Ralstonia solanacearum or even after its NLS-containing<br />
protein overexpression. Asit is well known that PCD requires a<br />
coordinate activation <strong>of</strong> different factors such as proteases and<br />
suppressors, NbCDM is likely to be one <strong>of</strong> such players inhibiting<br />
and modulating these processes.<br />
P11-015: GENERATION OF NITRIC OXIDE UNDER<br />
ANOXIA IS INDEPENDENT OF NITRATE REDUCTASE<br />
ACTIVITY.<br />
Kingston-Smith, A.* - Eelen, I. - Davies, T.E. - Mur, L.A.J. -<br />
Aberystwyth University<br />
*Corresponding author, e-mail: ahk@aber.ac.uk<br />
Exposure <strong>of</strong> plants to abiotic stress causes changes in foliar protein<br />
which can affect crop yield and quality. This is also true <strong>of</strong><br />
plant parts ingested by grazing ruminants whereby leaf cells are<br />
exposed to multiple stresses (heat, anoxia, microbial attack) in<br />
the hours following rumen entry causing autolysis. This has implications<br />
for the poor use <strong>of</strong> feed N by ruminants, which results<br />
in N deposition on land (as animal wastes) and contributes to<br />
N2O generation. As the cell signal NO has been implicated in<br />
cell death under biotic and abiotic stress this work investigated<br />
its potential role in control <strong>of</strong> autolysis in ingested plant cells.<br />
NO was detected in Arabidopsis thaliana Col-0 leaf discs after<br />
in vitro exposure to rumen-stress conditions. The source <strong>of</strong> NO<br />
generation in plants is currently unknown but could occur enzymically<br />
(catalysed by nitrate reductase; NR) or non-enzymically,<br />
an is enabled by an increase in intracellular nitrite under low oxygen<br />
conditions. The role <strong>of</strong> NR in NO generation under anoxia<br />
was determined by exposure <strong>of</strong> leaf discs from Col-0 and mutants<br />
Nia 1, Nia 2 and AtNos (which had 56%, 5% and 100%<br />
<strong>of</strong> NR activity <strong>of</strong> Col-0) to rumen-like conditions. NO was detectable<br />
by fluorescence microscopy in all lines after 1h. These<br />
results, plus no significant differences in foliar nitrite suggest that<br />
non-enzymic NO production in ingested plant cells could be responsible<br />
for autolysis.<br />
P11-016: ASYNCHRONOUS DEATH OF STOMATA<br />
GUARD CELLS PREDETERMINED BY THE ASYMME-<br />
TRIC OPEN MITOSIS<br />
Selga, T.* - Maija, S.<br />
Faculty <strong>of</strong> Biology, University <strong>of</strong> Latvia<br />
*Corresponding author, e-mail: turs.selga@lu.lv<br />
The control <strong>of</strong> programmed cell death (PCD) by previous asymmetric<br />
cell division (ACD) in plants is far from clear. The stomatal<br />
cell lineage is a typical example <strong>of</strong> precisely planned series<br />
<strong>of</strong> ACDs, that finish with as if symmetrical division <strong>of</strong> the guard<br />
mother cell (GMC) to form identical stomatal guard cells (GC)<br />
(Hove and Heidstua 2008, Nodeau 2009, Dong et al 2009) We<br />
searched among several hundreds <strong>of</strong> stomata in various stages<br />
<strong>of</strong> their development and senescence from the young, full grown<br />
and senescing leaves <strong>of</strong> tobacco (Nicotiana tabacum L.) by use<br />
<strong>of</strong> several methods and techniques <strong>of</strong> cyochemistry and microscopy.<br />
Our data suggests that the stomatal GMCs in reality always<br />
divide spatially asymmetrically by the classic open mitosis and<br />
develop unequal GCs, that age and die differently by different<br />
alterations <strong>of</strong> their nuclei and other organelles. Perinuclear endoplasmic<br />
reticulum in one <strong>of</strong> sister cells disappears faster than<br />
in another. The GMCs and GCs always are structurally joined at<br />
least with one nucleus <strong>of</strong> adjacent cell and migration <strong>of</strong> variously<br />
stained nuclear substance among them is evident. The permanent<br />
plastid-nuclear complex (PNCs) that we have repeatedly<br />
demonstrated in photosynthesizing cells <strong>of</strong> different vascular<br />
plants exists in all GMCs and GCs during all their lifespan, and<br />
evidently are important control units.<br />
P11-017: IDENTIFICATION OF PHOSPHORYLATED<br />
RESIDUES IN THE H+-ATPASE AND PHYSIOLOGICAL<br />
CONSEQUENCES OF THE EXPRESSION OF AN ACTI-<br />
VATED FORM IN THE PLANT<br />
Duby, G.* - Piette, A.S. - Piotrowiak, D. - Salladini, A. - Boutry, M.<br />
Institut des Sciences de la Vie, Université Catholique de Louvain<br />
*Corresponding author, e-mail: ge<strong>of</strong>frey.duby@uclouvain.be<br />
The plasma membrane H+-ATPase is building a proton electrochemical<br />
gradient that activates secondary transporters. It is involved,<br />
in cytosolic pH regulation, cell elongation and stomata<br />
aperture. It contains an auto-inhibitory C-terminal region and is