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 />
sible auxin and cytokinin interactions during root gravitropism<br />
are discussed.<br />
Project was supported with RFBR Grant No. 08-04-00566a,<br />
St.-Petersburg Government Grant for Young Researchers No.<br />
2.6/22-04/004.<br />
P06-005: THE ROLE OF APL AS A TRANSCRIPTIONAL<br />
REGULATOR IN SPECIFYING VASCULAR TISSUE<br />
IDENTITY<br />
Lichtenberger, R.* - Satu Lehesranta - Ove Lindgren - Sari Tähtiharju<br />
- Ykä Helariutta<br />
University <strong>of</strong> Helsinki<br />
*Corresponding author e-mail:raffael.lichtenberger@helsinki.fi<br />
The vascular system <strong>of</strong> higher plants confers efficient conduction<br />
and provides mechanical support. It consists <strong>of</strong> two kinds <strong>of</strong> conducting<br />
tissues, xylem and phloem. Phloem transports the products<br />
<strong>of</strong> photosynthesis and provides paths for translocation <strong>of</strong><br />
proteins and mRNAs involved in plant growth and development.<br />
Although there are some reports <strong>of</strong> gene expression characteristic<br />
to phloem, the molecular basis <strong>of</strong> phloem development is still<br />
largely unknown.<br />
The APL transcription factor (Altered Phloem Development) was<br />
identified as the first gene specifying vascular tissue identity. Based<br />
on cell sorting coupled with genome-wide microarray analysis,<br />
we have been able to uncover phloem abundant regulatory<br />
genes dependent on APL. The results indicate that APL is a key<br />
node for transcriptional activation <strong>of</strong> gene expression characteristic<br />
to phloem development and for transcriptional repression<br />
<strong>of</strong> gene expression characteristic to xylem development. We are<br />
currently studying the possible functions <strong>of</strong> the identified genes<br />
in phloem development.<br />
P06-006: MIR390, TAS3 TA-SIRNAS AND THEIR ARF<br />
TARGETS DEFINE AN AUTO-REGULATORY NET-<br />
WORK QUANTITATIVELY CONTROLLING LATERAL<br />
ROOT GROWTH<br />
Marin, E. 1 * - Jouannet, V. 2 - Herz, A. 3 - Lokerse, A.S. 4 - Weijers,<br />
D. 4 - Vaucheret, H. 5 - Nussaume, L. 3 - Crespi, M. 2 - Maizel, A. 2<br />
1<br />
(CEA)<br />
2<br />
Institut des Sciences du Végétal<br />
3<br />
Laboratoire de Biologie du Développement des Plantes, SBV-<br />
ME, IBEB, DSV, CEA, CNRS, Université Aix Marseille<br />
4<br />
Laboratory <strong>of</strong> Biochemistry, Wageningen University<br />
5<br />
Laboratoire de Biologie Cellulaire, Institut Jean-Pierre Bourgin<br />
*Corresponding author e-mail: elena.marin@cea.fr<br />
Plants adapt to environmental conditions by forming new organs<br />
in response to morphogenetic signals. Lateral roots branch from<br />
the main root in response to local auxin maxima. How a local<br />
auxin maximum translates to a robust pattern <strong>of</strong> gene activation<br />
ensuring the proper growth <strong>of</strong> the newly formed lateral root is<br />
not known. Here we demonstrate that miR390, TAS3-derived tasiRNAs<br />
(trans-acting siRNAs) and ARFs form an auxin-responsive<br />
regulatory network controlling lateral root growth. Spatial<br />
expression analysis using reporter gene fusions, ta-si/miRNA<br />
sensors and mutant analysis, showed that miR390 is specifically<br />
expressed at the sites <strong>of</strong> lateral root initiation where it triggers<br />
the biogenesis <strong>of</strong> trans-acting siRNAs. These ta-siRNAs inhibit<br />
ARF2, ARF3 and ARF4, thus releasing repression <strong>of</strong> lateral root<br />
growth. In addition, ARF2, ARF3 and ARF4 control auxin-induced<br />
miR390 accumulation.<br />
Positive and negative feedback regulation <strong>of</strong> miR390 by ARF2,<br />
ARF3 and ARF4 thus ensures the proper definition <strong>of</strong> the<br />
miR390 expression pattern and maintains ARF expression in a<br />
concentration range optimal for controlling the timing <strong>of</strong> lateral<br />
root growth, a function similar to its activity during leaf development.<br />
These results also show how small regulatory RNAs integrate<br />
with auxin signalling to quantitatively control organ growth<br />
during development.<br />
P06-007: THE INHIBITION OF PRIMARY ROOT ELON-<br />
GATION UNDER LOW BORON SUPPLY COULD BE ME-<br />
DIATED BY HORMONES IN ARABIDOPSIS SEEDLINGS<br />
Martín-Rejano, E.M. - Camacho-Cristóbal, J.J. - Herrera-Rodríguez,<br />
M.B. - Rexach, J. - Navarro-Gochicoa, M.T. - González-<br />
Fontes, A.<br />
Departamento de Fisiología, Anatomía y Biología Celular, Universidad<br />
Pablo de Olavide, E-41013, Sevilla, Spain<br />
*Corresponding author e-mail: emmarrej@upo.es<br />
Soil nutrients are critical elements for plant growth and productivity.<br />
Thus, in response to the bioavailability <strong>of</strong> nutrients in soils,<br />
plants have evolved various adaptive mechanisms among which<br />
the plastic development <strong>of</strong> the root system is <strong>of</strong> crucial importance.<br />
In this work we study in detail the temporal responses <strong>of</strong> the<br />
Arabidopsis root architecture to low boron (B) supply. For this<br />
purpose Arabidopsis seedlings were grown in 10 μM B during 5<br />
days and then transferred to a low B medium (0.4 mM) or control<br />
medium (10 mM) for a 4-day period. Neither the length nor the<br />
number <strong>of</strong> lateral roots were affected by B availability during the<br />
4 days <strong>of</strong> experiment; however, plants grown in the low B conditions<br />
had a reduced primary root (PR) length when compared<br />
to control plants from day 1 onwards. This is a very interesting<br />
result since lateral root growth should also be inhibited by low<br />
B supply if the primary effect <strong>of</strong> B was only on cell elongation<br />
(i.e. a consequence <strong>of</strong> the structural role <strong>of</strong> B in the cell wall).<br />
B availability also affected the number and elongation <strong>of</strong> roots<br />
hairs in the PR; thus, low B supply induced root hair proliferation<br />
and elongation.<br />
Furthermore, by using chemicals that alter hormone metabolism<br />
or signalling and several suitable mutants, we provide evidence<br />
showing that hormones could play a key role in the root architectural<br />
changes caused by low B availability.<br />
Research supported by BFU2009-08397 and Junta de Andalucía<br />
CVI-4721 and BIO-266, Spain<br />
P06-008: TOMATO MORPHOLOGICAL AND ANATO-<br />
MICAL ROOT TRAITS IN RELATION WITH PLANT<br />
WATER UPTAKE<br />
Romero Aranda, M. 1 * - Jurado-Lavado, O. 2 - Fernández-Muñoz, R. 2<br />
1<br />
Universidad de Málaga-Consejo Superior de Investigaciones<br />
Científicas (IHSM-UMA-CSIC), Estación Expe<br />
2<br />
Instituto de Hort<strong>of</strong>ruticultura Subtropical y Mediterránea “La<br />
Mayora”, Universidad de Málaga-Consejo Superior de Investigaciones<br />
Científicas (IHSM-UMA)<br />
*Corresponding author e-mail: rromero@eelm.csic.es<br />
Limited work has been performed to explore the potential for<br />
genetic improvement <strong>of</strong> tomato roots in relation to water uptake.<br />
The main goal <strong>of</strong> this study was to establish possible relationships<br />
between morphological or anatomical root characters and<br />
plant water uptake.<br />
We examined root traits in two tomato species (wild Solanum<br />
pimpinellifolium acc. TO-937 and domesticated Solanum lycopersicum<br />
cv. Moneymaker) differing in plant water use.<br />
The study was developed in a growth chamber in hydroponically<br />
cultivated plants which allowed assessing plant water uptake.<br />
Key root traits for water uptake, including root length and number<br />
<strong>of</strong> root tips were identify.<br />
Root anatomical traits, including root diameter, thickness <strong>of</strong> the<br />
cortex, number <strong>of</strong> xylem poles, number <strong>of</strong> metaxylem vessels<br />
and root and shoot biomass were also determined. In a period<br />
<strong>of</strong> 21 days, the cumulative plant water consumptions <strong>of</strong> TO-<br />
937 and Moneymaker were 1368±419 and 3209±696 ml/ plant,<br />
respectively. Shoot dry mass determined on Moneymaker was<br />
threefold that <strong>of</strong> TO-937 but root to shoot ratio were 0.17±0.03<br />
and 0.27±0.07 for Moneymakeer and TO-937, respectively. Plant<br />
water uptake and biomass production are discussed in relation<br />
with root development, root morphological traits and root internal<br />
anatomy.