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 />
P07-055: ANALYSIS OF ABIOTIC STRESS RESPONSES<br />
USING PROTEOMIC APPROACHES<br />
Hedtmann, C. 1 - Kaspar, S. 1 - Lippmann, R. 1 - Doell, S. 1 - Matros,<br />
A. 1 - Mock HP 1 - Witzel K 2<br />
1<br />
Leibniz Institute <strong>of</strong> Plant Genetics and Crop Plant Research<br />
2<br />
Instituts für Pflanzenernährung und Bodenkunde der Universität<br />
Kiel<br />
The presentation will focus on the application <strong>of</strong> proteomics performed<br />
on model and crop plants to elucidate mechanisms and<br />
traits related to abiotic stress tolerance. Although proteomics still<br />
is limited in comprehensiveness when compared with transcriptomics,<br />
it can provide valuable information not obtained by other<br />
“omics”-techniques. We apply 2-D gel based as well as LC-MSbased<br />
approaches to study the responses <strong>of</strong> plants towards abiotic<br />
stresses on the protein level. A major focus <strong>of</strong> recent work relates<br />
to the function <strong>of</strong> co-chaperones which are induced by various<br />
stresses. These co-chaperones with homology to the human<br />
HOP protein are represented as dimers and within larger protein<br />
complexes and are located both in the cytosol and the nucleus.<br />
Central for our further work is the use <strong>of</strong> the wide genetic diversity<br />
represented e.g. in the plant genebank <strong>of</strong> our institute. As<br />
an example, barley was evaluated for contrasting salt tolerance<br />
using mapping populations.<br />
P07-056: ARSENATE SIGNALLING IN ARABIDOPSIS<br />
THALIANA<br />
Leyva Tejada, A. - Castrillo Molina, G. - Pablo Catarecha, Z. -<br />
Eduardo Sánchez, B. - Leo Del Puerto, Y.<br />
Centro Nacional de Biotecnología-CSIC<br />
*Corresponding author e-mail: aleyva@cnb.csic.es<br />
In soils arsenic is primarily in the form <strong>of</strong> arsenate [As(V)] (Tamaki<br />
and Frankenberger, 1992, Brown et al 1999). Due to its<br />
chemical similarity to phosphate (Pi), As(V) is highly toxic to<br />
plants since it is readily incorporated through the high affinity<br />
phosphate transporter (McNair et al., 1992). This transport system<br />
is induced by Pi starvation and repressed in its presence.<br />
We have demonstrated that the genes induced by Pi are properly<br />
down regulated by As (V) (Catarecha et al 2007). In fact, some<br />
<strong>of</strong> these genes (Pi transporter PHT1;1 included), are repressed by<br />
As (V) more efficiently than by Pi. Analyzing the transcriptomic<br />
pr<strong>of</strong>ile <strong>of</strong> the As(V) response in Arabidopsis thaliana, we have<br />
found that this behavior occur at least in 10 % <strong>of</strong> the Pi-inducible-genes.<br />
These data indicates that in the case <strong>of</strong> As(V) and Pi<br />
their signaling mechanisms shares common elements. In order<br />
to identify these and others different elements, we start working<br />
in the characterization <strong>of</strong> mutants alters in the PHT1;1 repression<br />
by As(V). In this regard, we have analyzed the kinetics <strong>of</strong><br />
PHT1;1 repression using a transgenic line expressing the gen <strong>of</strong><br />
luciferase drive by PHT1;1 promoter. This tool provide us the<br />
possibility to concluded that this promoter are rapidly repressed<br />
by As(V) and in the case <strong>of</strong> Pi this repression is retarded (30<br />
min and 36 h respectively). In addition, the screening <strong>of</strong> an EMS<br />
mutagenized population expressing PHT1;1:LUC led us to the<br />
identification <strong>of</strong> mutants alters in the repression<br />
by As (V). The mapping <strong>of</strong> these genes will allow us the characterization<br />
<strong>of</strong> key elements in the As (V)<br />
perception.<br />
P07-057: MITOCHONDRIAL PROTEASE, ATFTSH4, IS<br />
REQUIRED FOR ARABIDOPSIS GROWTH AND DEVE-<br />
LOPMENT UNDER CONTINUAL MODERATE HEAT<br />
STRESS.<br />
Smakowska, E.* - Kicia, M. - Gibala, M, - Janska, H.<br />
University <strong>of</strong> Wroclaw<br />
*Corresponding author e-mail: elwira@ibmb.uni.wroc.pl<br />
We found, that a loss <strong>of</strong> mitochondrial AtFtsH4 protease significantly<br />
affect Arabidopsis growth and development under continual<br />
moderate heat stress (long days at 30oC). The ftsh4 mutant<br />
plants have shorter roots and stems, beside an emergence <strong>of</strong> true<br />
leaves but not cotyledons is delayed compared with wild-type<br />
plants. The true leaves are smaller and an important characteristic<br />
<strong>of</strong> the adult leaves is the asymmetric shape and irregular serration<br />
<strong>of</strong> leaf blades. Moreover, the inflorescence development <strong>of</strong> the<br />
ftsh4 plants growing at 30oC is arrested and, as a consequence,<br />
ftsh4 plants are unable to produce seeds.<br />
Although the growth and development <strong>of</strong> the ftsh4 mutants is<br />
highly susceptible to continual moderate heat stress, the mutants<br />
are not defective in acquired thermotolerance based on physiological<br />
experiments. In agreement with this result, the transcript<br />
level <strong>of</strong> AtHsp 101, which is a cytosolic heat shock protein required<br />
for acclimation to high temperature, is similar in the wild-type<br />
and ftsh4 when plants are exposed to both a short severe heat<br />
stress (1h, 38oC) or continual moderate heat stress (1-4 weeks,<br />
30oC). We also established that the mitochondrial AtFtsH4 protease<br />
is not a typical heat shock protein like Hsp101, because we<br />
haven’t found an increased accumulation <strong>of</strong> the AtFtsH4 transcripts<br />
upon a short time <strong>of</strong> high temperature stress. These results<br />
suggest that the thermosensitivity observed in the ftsh4 mutants<br />
is not caused by a defect in induction <strong>of</strong> cytosolic Hsp101 expression.<br />
P07-058: POLY ADP-RIBOSE POLYMERASE INVOLVE-<br />
MENT IN PROGRAMMED CELL DEATH OF TOBACCO<br />
BY-2 CELLS<br />
Locato, V. 1 - Cimini, S. 2 - Novo Uzal, E. 2 - de Pinto, M.C. 3 - Foyer,<br />
C.H. 4 - De Gara, L. 1<br />
1<br />
CIR-University Campus Bio-Medico di Roma<br />
2<br />
Departamento de Biología Animal, Vegetal y Ecología, Universidad<br />
de A Coruña<br />
3<br />
Dipartimento di Biologia e Patologia vegetale, Università di<br />
Bari<br />
4<br />
Centre <strong>of</strong> Plant Science, Leeds University, UK<br />
The term “programmed cell death” (PCD) refers to an apoptoticlike<br />
cell death that occurs during plant development and/or as<br />
consequence <strong>of</strong> various injuries. Plant PCD has many common<br />
features with animal apoptosis, but it also has some unique features<br />
related to the morphological and functional differences between<br />
the plant and animal systems. Like apoptosis, plant PCD<br />
initiation generally requires an accumulation <strong>of</strong> reactive oxygen<br />
species (ROS). Enhanced ROS production or depletion <strong>of</strong> antioxidants<br />
leads to oxidative stress, which can cause damage to<br />
cell structure and DNA. Moreover, ROS can act as molecular signals<br />
that regulate the progression <strong>of</strong> PCD. Animal and plant cells<br />
have defence and repair systems that counteract cell injury and<br />
DNA breakage. Poly-ADP ribosylation is a major process involved<br />
in DNA repair during oxidative stress and apoptosis that has<br />
been intensively studied in animal systems. However, little information<br />
is available on this process in plant cells. Here we report<br />
a study in which tobacco BY-2 cells were subjected oxidative<br />
stress-triggered PCD. Our results showed that poly ADP-ribose<br />
polymerase (PARP) activity was increased rapidly as consequence<br />
<strong>of</strong> oxidative stress. However, within hours <strong>of</strong> PCD activation<br />
PARP activity was decreased. PARP uses NAD+ to drive poly-<br />
ADP ribosylation. Thus, we suggest that regulated activation and<br />
deactivation <strong>of</strong> PARP might avoid energy depletion during PCD<br />
in order to sustain the energy-demanding death process.<br />
P07-059: LOOKING FOR CADMIUM TOLERANT MU-<br />
TANTS<br />
Agorio, A. 1 - Dardennes, J.S. 2 - Thomine, S. 1<br />
1<br />
Institut des Sciences du Végétal (CNRS)<br />
2<br />
Agroparistech<br />
Exposure to cadmium (Cd) has adverse health effects. Human<br />
uptake <strong>of</strong> Cd occurs mainly through the food-chain and tobacco<br />
smoke, as a consequence <strong>of</strong> heavy metal accumulation by crop