Estela Valle

Dr. Estela Valle


Research Focus & Metrics

Academic Career Length

45Years (1982-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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25 December 2007 in Plant Molecular Biology
Verified
Journal Article
Open access
PDF file
TSTelma E. Scarpeci
Telma E. Scarpeci
MZMaría I. Zanor
María I. Zanor
NCNéstor Carrillo
Néstor Carrillo
BMBernd Mueller-Roeber
Bernd Mueller-Roeber
EVEstela Valle
Estela Valle
The antioxidant defense system involves complex functional coordination of multiple components in different organelles within the plant cell. Here, we have studied the Arabidopsis thaliana early response to the generation of superoxide anion in chloroplasts during active photosynthesis. We exposed plants to methyl viologen (MV), a superoxide anion propagator in the light, and performed biochemical and expression profiling experiments using Affymetrix ATH1 GeneChip® microarrays under conditions in which photosynthesis and antioxidant enzymes were active. Data analysis identified superoxide-responsive genes that were compared with available microarray results. Examples include genes encoding proteins with unknown function, transcription factors and signal transduction components. A common GAAAAGTCAAAC motif containing the W-box consensus sequence of WRKY transcription factors, was found in the promoters of genes highly up-regulated by superoxide. Band shift assays showed that oxidative treatments enhanced the specific binding of leaf protein extracts to this motif. In addition, GUS reporter gene fused to WRKY30 promoter, which contains this binding motif, was induced by MV and H2O2. Overall, our study suggests that genes involved in signalling pathways and with unknown functions are rapidly activated by superoxide anion generated in photosynthetically active chloroplasts, as part of the early antioxidant response of Arabidopsis leaves.

21 June 2013 in Plant Molecular Biology
Verified
Journal Article
Closed access
PDF file
TSTelma E. Scarpeci
Telma E. Scarpeci
MZMaría I. Zanor
María I. Zanor
BMBernd Mueller-Roeber
Bernd Mueller-Roeber
EVEstela Valle
Estela Valle

7 July 2006 in The Plant Cell
Verified
Journal Article
Closed access
VTVanesa Beatriz Tognetti
Vanesa Beatriz Tognetti
JPJavier F. Palatnik
Javier F. Palatnik
MFMaría F. Fillat
María F. Fillat
MMMichael Melzer
Michael Melzer
MHMohammad-Reza Hajirezaei
Mohammad-Reza Hajirezaei
NCNéstor Carrillo
Néstor Carrillo
Chloroplast ferredoxin (Fd) plays a pivotal role in plant cell metabolism by delivering reducing equivalents to various essential oxidoreductive pathways. Fd levels decrease under adverse environmental conditions in many microorganisms, including cyanobacteria, which share a common ancestor with chloroplasts. Conversely, stress situations induce the synthesis of flavodoxin (Fld), an electron carrier flavoprotein not found in plants, which can efficiently replace Fd in most electron transfer processes. We report here that chloroplast Fd also declined in plants exposed to oxidants or stress conditions. A purified cyanobacterial Fld was able to mediate plant Fd-dependent reactions in vitro, including NADP+ and thioredoxin reduction. Tobacco (Nicotiana tabacum) plants expressing Fld in chloroplasts displayed increased tolerance to multiple sources of stress, including redox-cycling herbicides, extreme temperatures, high irradiation, water deficit, and UV radiation. Oxidant buildup and oxidative inactivation of thioredoxin-dependent plastidic enzymes were decreased in stressed plants expressing plastid-targeted Fld, suggesting that development of the tolerant phenotype relied on productive interaction of this flavoprotein with Fd-dependent oxidoreductive pathways of the host, most remarkably, thioredoxin reduction. The use of Fld provides new tools to investigate the requirements of photosynthesis in planta and to increase plant stress tolerance based on the introduction of a cyanobacterial product that is free from endogenous regulation in higher plants.

30 October 2009 in Amino Acids
Verified
Journal Article
Closed access
PDF file
ASAugusto Sorrequieta
Augusto Sorrequieta
GFGisela Ferraro PIBBA Ferraro
Gisela Ferraro PIBBA Ferraro
SBSilvana B. Boggio
Silvana B. Boggio
EVEstela Valle
Estela Valle

6 August 2008 in Plant Physiology
Verified
Journal Article
Closed access
HFHolger Fahnenstich
Holger Fahnenstich
TSTelma E. Scarpeci
Telma E. Scarpeci
EVEstela Valle
Estela Valle
UFUlf-Ingo Flügge
Ulf-Ingo Flügge
VMVerónica G. Maurino
Verónica G. Maurino
Arabidopsis (Arabidopsis thaliana) overexpressing glycolate oxidase (GO) in chloroplasts accumulates both hydrogen peroxide (H2O2) and glyoxylate. GO-overexpressing lines (GO plants) grown at 75 μmol quanta m−2 s−1 show retarded development, yellowish rosettes, and impaired photosynthetic performance, while at 30 μmol quanta m−2 s−1, this phenotype virtually disappears. The GO plants develop oxidative stress lesions under photorespiratory conditions but grow like wild-type plants under nonphotorespiratory conditions. GO plants coexpressing enzymes that further metabolize glyoxylate but still accumulate H2O2 show all features of the GO phenotype, indicating that H2O2 is responsible for the GO phenotype. The GO plants can complete their life cycle, showing that they are able to adapt to the stress conditions imposed by the accumulation of H2O2 during the light period. Moreover, the data demonstrate that a response to oxidative stress is installed, with increased expression and/or activity of known oxidative stress-responsive components. Hence, the GO plants are an ideal noninvasive model system in which to study the effects of H2O2 directly in the chloroplasts, because H2O2 accumulation is inducible and sustained perturbations can reproducibly be provoked by exposing the plants to different ambient conditions.

1 July 2003 in Plant Molecular Biology
Verified
Journal Article
Closed access
PDF file
MBMaria Busi
Maria Busi
CBClaudia Bustamante
Claudia Bustamante
CDCecilia D'Angelo
Cecilia D'Angelo
MHMauricio Hidalgo-Cuevas
Mauricio Hidalgo-Cuevas
SBSilvana B. Boggio
Silvana B. Boggio
EZEduardo Zabaleta
Eduardo Zabaleta