Book of Abstracts - Geyseco
Book of Abstracts - Geyseco
Book of Abstracts - Geyseco
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01 - PL - Plenary Sessions Lectures<br />
ago suggested the existence <strong>of</strong> a repressor <strong>of</strong> JA responses targeted<br />
by SCF COI1 for degradation by the proteasome in response<br />
to JA. Another important step in the pathway is represented by<br />
the transcription factor MYC2, which regulates several responses<br />
to JA. However, several key questions such as the link between<br />
these two steps in the pathway (MYC2 and SCF COI1 ), the nature<br />
<strong>of</strong> the bioactive hormone and the identity <strong>of</strong> its receptor remained<br />
unknown. We have recently identified a novel family <strong>of</strong> JA-regulated<br />
nuclear targets <strong>of</strong> SCF COI1 , named JAZ (Jasmonate ZIM-domain<br />
proteins). JAZ proteins are repressors <strong>of</strong> AtMYC2, linking<br />
the previous known steps in the pathway. Moreover, the identification<br />
<strong>of</strong> JAZ repressors has also paved the way to identify<br />
the jasmonate receptor (the F-box COI1) and the bioactive form<br />
<strong>of</strong> the hormone [(+)-7-iso-JA-Ile]. Recently, the identification <strong>of</strong><br />
a Novel-Interactor-<strong>of</strong>-JAZ proteins (NINJA) has uncovered the<br />
mechanism by which JAZ proteins repress MYC2 activity. How<br />
these discoveries help to understand the molecular mechanisms<br />
underlying JA-signalling will be discussed during the seminar.<br />
PL11: FROM PLANT-PATHOGEN INTERACTIONS TO<br />
ECOGENETICS OF PLANT-MICROBE COMMUNITIES<br />
Schulze-Lefert, P.*<br />
Max Plankc Institute for Plant Breeding Research, Köln, Germany<br />
*Corresponding author, e-mail: schlef@mpiz-koeln.mpg.de<br />
Parasitic and symbiotic associations between plants and microbes<br />
are merely the two extreme outcomes <strong>of</strong> a continuum <strong>of</strong><br />
inter-organismal interactions affecting plant productivity. Little<br />
is understood about plant-microbe interactions that are, at first<br />
glance, symptomless. Complex communities <strong>of</strong> poorly studied<br />
plant-associated microbes are an untapped reservoir that can promote<br />
plant health and productivity. We have begun to examine<br />
the microbiome <strong>of</strong> the Arabidopsis rhizosphere using T-RFLP<br />
and 454 pyrosequencing pr<strong>of</strong>iling methods. I will describe the<br />
structure <strong>of</strong> root-associated bacterial communities found in natural<br />
soil and our attempts to examine the genetic basis <strong>of</strong> their<br />
formation.<br />
PL12: MECHANISMS AND PHENOTYPIC CONSE-<br />
QUENCES OF DNA METHYLATION IN ARABIDOPSIS<br />
Colot, V.*<br />
Institut de Biologie de l’Ecole Normale Supérieure (IBENS),<br />
CNRS, Paris, France<br />
*Corresponding author, e-mail: colot@biologie.ens.fr<br />
DNA methylation plays key roles in the control <strong>of</strong> genome activity<br />
in plants and mammals. It is critical for the stable silencing <strong>of</strong><br />
repeat elements and is also involved in the epigenetic regulation<br />
<strong>of</strong> some genes. Despite similarities in the controlling functions <strong>of</strong><br />
DNA methylation, its dynamics and deposition patterns differ in<br />
several respects between plants and mammals. One <strong>of</strong> the most<br />
striking differences is that plants tend to propagate pre-existing<br />
DNA methylation states across generations, whereas mammals<br />
re-establish them genome wide at every generation. Our recent<br />
findings on the transgenerational stability <strong>of</strong> DNA methylation<br />
patterns in Arabidopsis will be presented. The role <strong>of</strong> RNAi in<br />
the incremental methylation and silencing <strong>of</strong> repeat elements<br />
over successive generations and in the preservation <strong>of</strong> normal<br />
expression <strong>of</strong> neighboring genes will be highlighted<br />
PL13: MAKING OIL IN BIOMASS BY REGULATING<br />
FATTY ACID BREAKDOWN AND LIPID SYNTHESIS PA-<br />
THWAYS.<br />
Graham, I; Slocombe, S; He, Z; Dyer, J; Hernandez, L; Larson, TR.<br />
University <strong>of</strong> York<br />
*Corresponding author, e-mail: iag1@york.ac.uk<br />
Plant oils in the form <strong>of</strong> triacylglycerol (TAG) are used for food,<br />
industrial feedstock and bi<strong>of</strong>uel manufacture. Although TAG is<br />
typically harvested from the fruit or seeds <strong>of</strong> oil crop species,<br />
plants can also accumulate small amounts <strong>of</strong> TAG in the leaves<br />
and other vegetative tissues. Partitioning <strong>of</strong> fatty acids into TAG<br />
involves several endoplasmic reticulum associated acyltransferases.<br />
We have found that when fatty acid breakdown is blocked<br />
in seedlings <strong>of</strong> the model plant Arabidopsis, recycling <strong>of</strong><br />
fatty acids back into oil body TAG occurs. A soluble cytosolic<br />
acyltransferase appears to be involved in this process. In older<br />
vegetative leaves, we have found that TAG levels can be increased<br />
significantly (10–20 fold) by blocking fatty acid breakdown,<br />
particularly during extended dark treatments or leaf senescence.<br />
Generation <strong>of</strong> a double mutant in fatty acid breakdown and diacylglycerol<br />
acyltransferase 1 (DGAT1) results in a severe vegetative<br />
growth phenotype suggesting that partitioning <strong>of</strong> fatty acids<br />
to TAG in leaves is carried out predominantly by this acyltransferase.<br />
Ectopic expression <strong>of</strong> LEC2, a seed development transcription<br />
factor involved in storage product accumulation results<br />
in accumulation <strong>of</strong> seed oil type species <strong>of</strong> TAG in senescing<br />
tissue that are blocked in fatty acid breakdown. Our data suggests<br />
that recycled membrane fatty acids can be re-directed to TAG by<br />
expressing the seed-programme in senescing tissue or by a block<br />
in fatty acid breakdown. This work raises the possibility <strong>of</strong> producing<br />
significant amounts <strong>of</strong> oil in vegetative tissues <strong>of</strong> biomass<br />
crops such as Miscanthus.<br />
PL14: PLANTS RESPONSES TO GLOBAL CHANGE<br />
Valladares, F.*<br />
Instituto Recursos Naturales CSIC<br />
*Corresponding author, e-mail: valladares@ccma.csic.es<br />
Current environmental change is having important impacts on<br />
plant performance. Global change involves not only a general<br />
trend <strong>of</strong> increasing air temperatures but also an increased frequency<br />
<strong>of</strong> extreme climatic events, habitat fragmentation and<br />
degradation, and high rates <strong>of</strong> biotic exchange leading to assemblages<br />
<strong>of</strong> novel communities <strong>of</strong> plants, animals and microorganisms.<br />
Plant responses to these changes involve plastic phenotypic<br />
changes (e.g. acclimation), passive tolerance <strong>of</strong> the increased<br />
stress, rapid microevolutionary changes, and, if all this fails,<br />
local extinctions. There are two main novelties <strong>of</strong> global change<br />
pressures for plants: the speed <strong>of</strong> the environmental change<br />
and the fact that it involves changes in several biotic and abiotic<br />
factors simultaneously. While plant stress physiology has promoted<br />
active research, plant physiology under multiple stresses<br />
still requires extensive attention. I illustrate what we know and<br />
what we should know about plant physiology under global change<br />
conditions with examples <strong>of</strong> Mediterranean ecosystems where<br />
water limitations are exacerbated by climate change. Impacts <strong>of</strong><br />
changing water availabilities coupled to changes in the light environment<br />
are mediated by other co-occurring factors such as soil<br />
fertility and air temperature, but also by the presence and performance<br />
<strong>of</strong> other competing or symbiotic organisms. Co-existing<br />
plants can either facilitate or outcompete the study species and<br />
the stress level imposed by water is pr<strong>of</strong>oundly affected by organisms<br />
in the soil.<br />
PL15: MECHANISTIC ANALYSIS OF THE ENDODER-<br />
MIS AS A SELECTIVE AND PROTECTIVE ROOT-SOIL<br />
INTERFACE<br />
Geldner, N.*<br />
University <strong>of</strong> Lausanne<br />
*Corresponding author, e-mail: Niko.Geldner@unil.ch<br />
We analyse the molecular mechanisms that underlie the development<br />
and function <strong>of</strong> the root endodermis in Arabidopsis. The endodermis<br />
is a cell layer in the root <strong>of</strong> all higher plants and thought<br />
to be <strong>of</strong> central importance for plant nutrition and stress resistance.<br />
We have established molecular markers which demonstrate<br />
that the endodermal plasma membrane has two separate polar<br />
domains <strong>of</strong> distinct function. Our description <strong>of</strong> endodermal<br />
PL