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 />
PS03: SYSTEMS BIOLOGY &<br />
Omics<br />
Session lead lectures<br />
PS03-001: SYSTEMS ANALYSIS OF THE CONTRIBU-<br />
TION OF METABOLISM TO GROWTH IN ARABIDOP-<br />
SIS<br />
Stitt, M.*<br />
Max Planck Institute <strong>of</strong> Molecular Plant Physiology, Golm, Germany<br />
*Corresponding author, e-mail: stitt@mpimp-golm.mpg.de<br />
Plants are exposed to a continually changing environment, including<br />
the diurnal light-dark cycle, and changes that are superimposed<br />
on this cycle. Starch provides the major carbon store<br />
for growth at night. We have used ‘omics analysis <strong>of</strong> responses<br />
during the diurnal cycle to investigate how growth is coordinated<br />
with the momentary and longer-term changes in the carbon.<br />
Thousands <strong>of</strong> transcripts show large diurnal changes <strong>of</strong> their<br />
levels. These can be predicted using a simple linear model, in<br />
which the clock, sugar and light as the major inputs. Some <strong>of</strong><br />
the most striking and best-predicted changes are for genes involved<br />
in protein synthesis. Polysome analyses reveal that the<br />
global translation rate is tightly tied to the momentary carbon<br />
availability. To explore the relation between translation and plant<br />
growth more closely, we have carried out quantitative analyses<br />
<strong>of</strong> rRNA, transcripts, polysome loading and protein abundance.<br />
This allows us to model the relationship between basic molecular<br />
parameters like ribosome and transcript concentrations and<br />
the whole plant carbon budget and growth. The results show that<br />
protein synthesis represents a significant component <strong>of</strong> the total<br />
plant energy budget, and is regulated to optimise energy costs<br />
on a diurnal basis, and probably also during long term adaptations<br />
to environmental conditions. These results receive independent<br />
support from a complementary approach, in which we<br />
have identified integrative molecular and metabolic parameters<br />
that determine biomass production in a panel <strong>of</strong> 100 Arabidopsis<br />
accessions. These reveal that starch and protein are correlated<br />
with each other, act as integrators <strong>of</strong> the metabolic response, and<br />
are negatively correlated with rosette biomass, and also reveal a<br />
strong impact <strong>of</strong> ribosome abundance and the efficiency <strong>of</strong> ribosome<br />
use on biomass formation.<br />
PS03-002: CONSTRAINT BASED MODELLING – A NEW<br />
APPROACH TO SYSTEMS-LEVEL STUDY OF PLANT<br />
METABOLIC NETWORK<br />
Zhu, X.*<br />
CAS-MPG Partner Institute for Computational Biology<br />
*Corresponding author, e-mail: zhuxinguang@picb.ac.cn<br />
Identifying new ways to improve photosynthesis is one feasible<br />
approach to increase crop potential yields. Building dynamic<br />
systems models <strong>of</strong> photosynthesis and plant primary metabolism<br />
is one option to identify targets to increase photosynthesis. This<br />
method however is <strong>of</strong>ten limited by the shortage <strong>of</strong> kinetic parameters,<br />
which demands development <strong>of</strong> high throughput methods<br />
to characterize the compartment-specific information about<br />
the metabolomics, proteomics and enzyme activities related to<br />
photosynthesis and plant primary metabolism. Constraint based<br />
modelling on the contrary requires less detailed kinetic information.<br />
It has been used widely in microbiology community to<br />
study metabolism and regulation at a genomic scale. A few constraint<br />
based models have been developed in the last five years to<br />
study plant metabolic network properties. In this lecture, I will<br />
briefly discuss the concept, methodology, major applications and<br />
challenges <strong>of</strong> using this approach in plant biology research. The<br />
potential <strong>of</strong> linking this method to high throughput data to sudy<br />
the response <strong>of</strong> plants to climate change and identifying new options<br />
to increase photosynthesis will be discussed.<br />
PS04: REPRODUCTIVE DEVE-<br />
LOPMENT<br />
Session lead lectures<br />
PS04-001: SELF-INCOMPATIBILITY SIGNALLING NET-<br />
WORKS: CONVERSATIONS THAT TELL “SELF” PO-<br />
LLEN TO COMMIT SUICIDE<br />
Wheeler, M.J. - de Graaf, B.H.J. - Wu, J. - Poulter N.S. - Wilkins,<br />
K.A. - Vatovec, S. - Franklin-Tong, V.*<br />
University <strong>of</strong> Birmingham<br />
*Corresponding author, e-mail: v.e.franklin-tong@bham.ac.uk<br />
Self-incompatibility (SI) is controlled by a multi-allelic S locus<br />
that allows discrimination between “self” pollen from “non-self”<br />
pollen. In Papaver rhoeas, the pistil S determinant (recently renamed<br />
as PrsS, Papaver rhoeas stigma S) encodes a small novel<br />
protein that interacts with incompatible pollen, triggering a Ca 2+ -<br />
dependent signalling network. We recently identified the Papaver<br />
pollen S-determinant (Papaver rhoeas pollen S), PrpS, which<br />
encodes a novel ~20 kDa transmembrane protein with no homology<br />
to sequences in existing databases. I will present our data<br />
showing that PrpS has the attributes expected <strong>of</strong> a pollen S locus<br />
determinant, including functional data5. I will also present recent<br />
data suggesting that PrsS acts as a ligand, stimulating non-specific<br />
cation conductance permeable to Ca 2+ and K + . Downstream <strong>of</strong><br />
interaction <strong>of</strong> PrsS with PrpS, we have identified several events<br />
that are triggered specifically in an incompatible situation. These<br />
include rapid alterations to the actin cytoskeleton 1,2 and programmed<br />
cell death, involving caspase-like activities 3,4. I will present<br />
unpublished data identifying further SI-specific events triggered<br />
in incompatible pollen. We have recently begun studies <strong>of</strong> PrpS<br />
in Arabidopsis and I will present preliminary data showing that<br />
poppy SI appears to function in Arabidopsis.<br />
References<br />
1. Snowman BN, et al. (2002) Plant Cell 14, 2613-2626.<br />
2. Poulter NS, et al (2010) Plant Physiol 10.1104/pp.109.152066<br />
3. Bosch, M. & Franklin-Tong, V. E. (2007) PNAS 104, 18327-<br />
18332.<br />
4. Thomas, S. G. & Franklin-Tong, V. E. (2006) Nature 429, 305-<br />
309.<br />
5. Wheeler, M. J. et al. (2009) Nature 459, 992-995.<br />
PS04-002: CELL-CELL COMMUNICATION DURING<br />
FERTILIZATION IN ARABIDOPSIS: A SURPRISING<br />
LINK TO DISEASE RESISTANCE<br />
Kessler, S. 1 - Escobar-Restrepo, J. M. 1 - Huck, N. 1 - Asano, H. 1 -<br />
Kienath, N. F. 2 - Panstruga, R. 2 - Grossniklaus, U. 1 *<br />
1Institute <strong>of</strong> Plant Biology & Zürich-Basel Plant Science Center,<br />
University <strong>of</strong> Zürich<br />
2Max-Planck Institute for Plant Breeding Research, Cologne<br />
*Corresponding author, e-mail: grossnik@botinst.uzh.ch<br />
Research in our laboratory focuses on the developmental genetics<br />
<strong>of</strong> plant reproduction. Our studies have shown that both<br />
genetic and epigenetic mechanisms play a key role in plant reproduction.<br />
We have isolated a female gametophytic mutant,<br />
feronia, which disrupts double fertilization: in feronia mutant<br />
embryo sacs the pollen tubes, even if wild-type, are unable to<br />
release the sperm cells to effect fertilization (Huck et al., 2003,<br />
Development 130: 2149). This phenotype suggests that the female<br />
gametophyte plays a crucial role in pollen tube reception and,<br />
thus, controls the behaviour <strong>of</strong> the male gametophyte. The feronia<br />
mutant defines novel signalling processes between the male<br />
and female gametophytes in the process <strong>of</strong> double fertilization<br />
FERONIA was shown to encode a receptor-like kinase <strong>of</strong> a plantspecific<br />
subfamily (Escobar-Restrepo et al., 2007, Science 317:<br />
656). Interestingly, some interspecific crosses result in phenotypes<br />
that are very similar to those observed in the feronia mutant.<br />
I will report on the molecular and biochemical characterization