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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 />

gene-specific primers for six <strong>of</strong> the nine ZmASRs identified in<br />

the maize genome showed that ZmASR1 was the major expressed<br />

is<strong>of</strong>orm in leaves and kernels. We found that up-regulation<br />

by drought in leaves was a common feature to all ZmASRs, except<br />

ZmASR3, in contrast to kernels where only ZmASR2 transcript<br />

levels increased. Transgenic maize plants over-expressing<br />

ZmASR1 (ZmASR1-OE) displayed increased shoot biomass yield<br />

under fully irrigated condition and increased ear leaf area, kernel<br />

yield weight and kernel number under both fully irrigated and<br />

water-limited conditions in the field. Comparative transcriptomic<br />

and proteomic analyses <strong>of</strong> ZmASR1-OE and wild-type sister<br />

leaves led to the conclusion that ZmASR1-OE triggers small-scale<br />

changes on the transcriptional and protein levels that concern<br />

mainly genes involved in the raffinose family oligosaccharides or<br />

branched-chain amino acid metabolic pathways.<br />

Metabolomic analysis confirmed the impact <strong>of</strong> ZmASR1-OE on<br />

these pathways and revealed that ZmASR1-OE decreased the levels<br />

<strong>of</strong> metabolites displaying a negative correlation to biomass<br />

in Arabidopsis. Collectively, these data demonstrate the feasibility<br />

<strong>of</strong> engineering drought stress tolerance and yield new insights<br />

into the function <strong>of</strong> the ZmASR1 protein.<br />

S02-001: DISSECTING THE MOLECULAR REGULA-<br />

TION OF CORK CAMBIUM<br />

Miguel, A.¹* - Milhinhos, A.¹ - Pinto Ricardo, C.² - Jones, B.³ -<br />

Miguel, C.¹<br />

¹IBET/ITQB-UNL<br />

²ITQB-UNL<br />

³University <strong>of</strong> Sydney-Australia/UPSC-Sweden<br />

*Corresponding author e-mail: andreiamiguel@itqb.unl.pt<br />

In plant stems, the cork cambium usually initiates in the subepidermis.<br />

Cork cambium cells divide periclinally, giving rise<br />

to phelloderm cells on the inside and to phellem (cork) cells on<br />

the outside. Together, the cork cambium, cork and phelloderm<br />

form the periderm which protects the live tissues from damaging<br />

factors. Cork extracted from the cork oak is also a renewable<br />

material <strong>of</strong> high economic value due to its unique properties. Our<br />

major goal is to identify molecular regulators <strong>of</strong> this lateral meristem<br />

and we are presently focusing on the role <strong>of</strong> a few transcription<br />

factors, namely SHORT-ROOT (SHR) from the GRAS<br />

family. This gene has been extensively studied in the Arabidopsis<br />

root where it is described as a key component in the developmental<br />

pathway regulating the specification <strong>of</strong> the root stem<br />

cell niche and radial patterning (1, 2, 3). Through an integrated<br />

approach combining cell biology and gene expression characterization<br />

tools we aim to provide evidence <strong>of</strong> the putative involvement<br />

<strong>of</strong> SHR in the regulation <strong>of</strong> cork cambium. SHR sequences<br />

have been cloned from poplar and cork oak transcriptome and<br />

the effects <strong>of</strong> down-regulation and ectopic expression <strong>of</strong> SHR in<br />

transgenic poplar lines are being investigated. A comparative<br />

analysis <strong>of</strong> SHR expression patterns in poplar and cork oak will<br />

be conducted in order to validate the use <strong>of</strong> poplar as a model for<br />

these studies. References: 1. Benfey PN, et al. (1993) Development<br />

119: 57-70; 2. Helariutta Y, et al. (2000) Cell 101: 555-567;<br />

3. Nakajima K, et al. (2001) Nature 413: 307-311.<br />

Acknowledgments: Financial support provided by FCT through<br />

project PTDC/AGRGPL/ 098369/2008 and grant SFRH/<br />

BD/44474/2008.<br />

S02-002: INSIGHTS IN THE DISCOVERY OF NOVEL RE-<br />

GULATORS THAT CONTROL PLANT ARCHITECTURE<br />

Alos Ros, E.* - Wigge, P. - Kumar, V. - Lucyshyn, D.<br />

John Innes Cente<br />

*Corresponding author e-mail: enriqueta.alos@bbsrc.ac.uk<br />

In Arabidopsis, a key role in maintaining indeterminate vegetative<br />

meristems is carried out by a molecule closely related<br />

to FLOWERING LOCUS T (FT), TERMINAL FLOWER 1<br />

(TFL1), that acts in combination ith FD to repress expression <strong>of</strong><br />

flowering genes. While mutants that lack FT are very late flowering,<br />

tfl1 mutations have the opposite phenotype, causing the<br />

plants to flower early and terminate their growth with a pr<strong>of</strong>usion<br />

<strong>of</strong> flowers, resembling gain-<strong>of</strong>-function plants (1, 2, 3).<br />

To address both plant architecture and the limiting role <strong>of</strong> FT<br />

in plant development, we have performed a genetic screen for<br />

flowering time and architecture mutants in the - 1 background.<br />

3400 M2 families have been screened and 20 mutants selected as<br />

modifiers <strong>of</strong> the tfl1-1 phenotype. Amongst the isolated mutants,<br />

mutations in already described genes have been identified such<br />

as APETALA 1 and LEAFY. Interestingly, novel modifiers <strong>of</strong> the<br />

tfl1-1 phenotype have been obtained and mapped. The functional<br />

characterization and the roles <strong>of</strong> these genes in plant architecture<br />

are discussed in the present work.<br />

1. Bradley, D., Ratcliffe, O., Vincent, C., Carpenter, R., and<br />

Coen, E. (1997). Science 275, 80-83.<br />

2. Kardailsky, I., Shukla, V.K., Ahn, J.H., Dagenais, N., Christensen,<br />

S.K., Nguyen, J.T., Chory, J., Harrison, M.J., and Weigel, D.<br />

(1999). Science 286, 1962-1965.<br />

3. Prusinkiewicz, P., Erasmus, Y., Lane, B., Harder, L.D., and<br />

Coen, E. (2007). Science 316, 1452-1456.<br />

S02-003: CLOCK-MEDIATED CONTROL OF GIBBERE-<br />

LLIN RESPONSES IN ARABIDOPSIS<br />

Arana, M. V. ¹* - Marín, Nora A.¹ - Malo<strong>of</strong>, J. N.² - Alabadi, D.¹<br />

- Blázquez, M.A.<br />

¹IBMCP - Universidad Politécnica de Valencia. Valencia. España<br />

²Section <strong>of</strong> Plant Biology, College <strong>of</strong> Biological Sciences, University<br />

<strong>of</strong> California, Davis<br />

*Corresponding author e-mail: arana@agro.uba.ar<br />

The circadian clock acts as central coordinator <strong>of</strong> plant activity,<br />

and it regulates key traits for plant fitness such as seed germination,<br />

gas exchange, flowering and growth.<br />

Particularly, growth <strong>of</strong> germinating seedlings is restricted to certain<br />

times <strong>of</strong> the day, showing a maximum rate near dawn. This<br />

pattern can be explained by the lightmediated degradation <strong>of</strong> PIF<br />

proteins during the day combined with the clock-mediated repression<br />

<strong>of</strong> PIF transcript accumulation early in the night. This<br />

combined action yields high levels <strong>of</strong> PIF proteins at the end <strong>of</strong><br />

the night, which are responsible for growth. In addition to this<br />

mechanism, growth is controlled by several plant hormones such<br />

as gibberellins (GA), auxins and brassinosteroids, and GA action<br />

has been shown to involve the relief <strong>of</strong> the DELLA-mediated<br />

inhibition <strong>of</strong> PIF transcriptional activity. Although GA signaling<br />

has been thoroughly studied in constant environments its contribution<br />

to plant growth under predictable daily environmental<br />

changes such as day/night cycles is still unknown. Here we show<br />

that the circadian clock gates hypocotyl GA sensitivity, resulting<br />

in the promotion <strong>of</strong> GA signaling late in the night, the moment<br />

when maximum growth occurs. This effect involves the transcriptional<br />

control <strong>of</strong> the GA receptors and influences both the<br />

daily patterns <strong>of</strong> DELLA accumulation and the rate <strong>of</strong> hypocotyl<br />

elongation. Taken together, our results show that anticipation<br />

<strong>of</strong> biological events to external day and night cycles requires a<br />

functional GA signaling, and that the GA pathway is a relevant<br />

clock output for the control early plant developmental traits, such<br />

as daily growth rhythms.<br />

S02-004: DEVELOPMENT AND VALIDATION OF A SEN-<br />

SITIVE AND RAPID METHOD FOR THE DETERMINA-<br />

TION OF UNLABELED AND DEUTERIUM LABELED<br />

PLANT HORMONES IN DIFFERENT PLANT TISSUES<br />

USING UPLC-MS/MS<br />

Müller, M. * - Munné-Bosch, S.<br />

University <strong>of</strong> Barcelona<br />

*Corresponding author e-mail: maren.muller@ub.edu<br />

Plant hormones play a pivotal role in several physiological processes<br />

during a plant’s life cycle, from germination to senes-

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