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Dive into the research topics where Sarah Jane Cookson is active.

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Featured researches published by Sarah Jane Cookson.


Journal of Experimental Botany | 2014

Heterografting with nonself rootstocks induces genes involved in stress responses at the graft interface when compared with autografted controls

Sarah Jane Cookson; M. J. Clemente Moreno; Cyril Hevin; L. Z. Nyamba Mendome; Serge Delrot; N. Magnin; Claudine Trossat-Magnin; Nathalie Ollat

Summary Grafting together two different genotypes results in the upregulation of stress responses at the graft interface during graft union formation in comparison to the wound-like responses of autografts.


Journal of Experimental Botany | 2013

Graft union formation in grapevine induces transcriptional changes related to cell wall modification, wounding, hormone signalling, and secondary metabolism

Sarah Jane Cookson; Maria José Clemente Moreno; Cyril Hevin; Larissa Zita Nyamba Mendome; Serge Delrot; Claudine Trossat-Magnin; Nathalie Ollat

Grafting is particularly important to the cultivation of perennial crops such as grapevine (Vitis vinifera) because rootstocks can provide resistance to soil-borne pests and diseases as well as improve tolerance to some abiotic stresses. Successful grafting is a complex biochemical and structural process beginning with the adhesion of the two grafted partners, followed by callus formation and the establishment of a functional vascular system. At the molecular level, the sequence of events underlying graft union formation remains largely uncharacterized. The present study investigates the transcriptome of grapevine rootstock and graft interface tissues sampled 3 d and 28 d after grafting of over-wintering stems in the spring. Many genes were differentially expressed over time, from 3 d to 28 d after grafting, which could be related to the activation of stem growth and metabolic activity in the spring. This hypothesis is supported by the up-regulation of many genes associated with cell wall synthesis, and phloem and xylem development. Generally, there was an up-regulation of gene expression in the graft interface tissue compared with the rootstock, particularly genes involved in cell wall synthesis, secondary metabolism, and signalling. Although there was overlap between the genes differentially expressed over time (from 3 d to 28 d after grafting) with the gene differentially expressed between the rootstock and the graft interface, numerous graft interface-specific genes were identified.


Plant Cell and Environment | 2011

Do pH changes in the leaf apoplast contribute to rapid inhibition of leaf elongation rate by water stress? Comparison of stress responses induced by polyethylene glycol and down-regulation of root hydraulic conductivity

Christina Ehlert; Claude Plassard; Sarah Jane Cookson; Francois Tardieu; Thierry Simonneau

We have dissected the influences of apoplastic pH and cell turgor on short-term responses of leaf growth to plant water status, by using a combination of a double-barrelled pH-selective microelectrodes and a cell pressure probe. These techniques were used, together with continuous measurements of leaf elongation rate (LER), in the (hidden) elongating zone of the leaves of intact maize plants while exposing roots to various treatments. Polyethylene glycol (PEG) reduced water availability to roots, while acid load and anoxia decreased root hydraulic conductivity. During the first 30 min, acid load and anoxia induced moderate reductions in leaf growth and turgor, with no effect on leaf apoplastic pH. PEG stopped leaf growth, while turgor was only partially reduced. Rapid alkalinization of the apoplast, from pH 4.9 ± 0.3 to pH 5.8 ± 0.2 within 30 min, may have participated to this rapid growth reduction. After 60 min, leaf growth inhibition correlated well with turgor reduction across all treatments, supporting a growth limitation by hydraulics. We conclude that apoplastic alkalinization may transiently impair the control of leaf growth by cell turgor upon abrupt water stress, whereas direct hydraulic control of growth predominates under moderate conditions and after a 30-60 min delay following imposition of water stress.


Functional Plant Biology | 2012

Grapevine rootstock effects on scion biomass are not associated with large modifications of primary shoot growth under nonlimiting conditions in the first year of growth

Sarah Jane Cookson; Cyril Hevin; Martine Donnart; Nathalie Ollat

In grapevine (Vitis vinifera L.), rootstocks are known to alter scion development by modifying stem weight and yield. The aim of this work was to evaluate the contribution of primary growth to the rootstock effects on scion biomass. The shoot growth of Vitis vinifera cv. Cabernet Sauvignon N autografted and grafted onto Vitis riparia cv. Riparia Gloire de Montpellier and Vitis berlandieri×V. rupestris cv. 1103 Paulsen was studied in young plants grown in pots trained to one stem in two experiments. Stem elongation and phytomer emergence were studied from grafting until the end of the growth season. The elongation of the Cabernet Sauvignon N leaves, tendrils and internodes of each phytomer along the stem was fitted using sigmoid curves. The rootstocks studied slightly altered the growth dynamics of the leaves, internodes and tendrils of the scion. This is the first study to examine the effect of rootstocks on shoot growth dynamics in any species. The alterations in primary growth were small, suggesting that rootstocks may alter scion biomass principally by modifying secondary growth.


BMC Plant Biology | 2016

ABA-mediated responses to water deficit separate grapevine genotypes by their genetic background

Landry Rossdeutsch; Everard Edwards; Sarah Jane Cookson; François Barrieu; Gregory A Gambetta; Serge Delrot; Nathalie Ollat

BackgroundABA-mediated processes are involved in plant responses to water deficit, especially the control of stomatal opening. However in grapevine it is not known if these processes participate in the phenotypic variation in drought adaptation existing between genotypes. To elucidate this question, the response to short-term water-deficit was analysed in roots and shoots of nine Vitis genotypes differing in their drought adaptation in the field. The transcript abundance of 12 genes involved in ABA biosynthesis, catabolism, and signalling were monitored, together with physiological and metabolic parameters related to ABA and its role in controlling plant transpiration.ResultsAlthough transpiration and ABA responses were well-conserved among the genotypes, multifactorial analyses separated Vitis vinifera varieties and V. berlandieri x V. rupestris hybrids (all considered drought tolerant) from the other genotypes studied. Generally, V. vinifera varieties, followed by V. berlandieri x V. rupestris hybrids, displayed more pronounced responses to water-deficit in comparison to the other genotypes. However, changes in transcript abundance in roots were more pronounced for Vitis hybrids than V. vinifera genotypes. Changes in the expression of the cornerstone ABA biosynthetic gene VviNCED1, and the ABA transcriptional regulator VviABF1, were associated with the response of V. vinifera genotypes, while changes in VviNCED2 abundance were associated with the response of other Vitis genotypes. In contrast, the ABA RCAR receptors were not identified as key components of the genotypic variability of water-deficit responses. Interestingly, the expression of VviSnRK2.6 (an AtOST1 ortholog) was constitutively lower in roots and leaves of V. vinifera genotypes and higher in roots of V. berlandieri x V. rupestris hybrids.ConclusionsThis study highlights that Vitis genotypes exhibiting different levels of drought adaptation differ in key steps involved in ABA metabolism and signalling; both under well-watered conditions and in response to water-deficit. In addition, it supports that adaptation may be related to various mechanisms related or not to ABA responses.


Wiley Interdisciplinary Reviews-Developmental Biology | 2013

Phenotyping the kinematics of leaf development in flowering plants: recommendations and pitfalls.

Maryline Lièvre; Nathalie Wuyts; Sarah Jane Cookson; Justine Bresson; Mélanie Dapp; François Vasseur; Catherine Massonnet; Sébastien Tisné; Mathilde Bettembourg; Crispulo Balsera; Alexis Bédiée; Frédéric Bouvery; Myriam Dauzat; Gaëlle Rolland; Denis Vile; Christine Granier

Leaves of flowering plants are produced from the shoot apical meristem at regular intervals and they grow according to a developmental program that is determined by both genetic and environmental factors. Detailed frameworks for multiscale dynamic analyses of leaf growth have been developed in order to identify and interpret phenotypic differences caused by either genetic or environmental variations. They revealed that leaf growth dynamics are non‐linearly and nonhomogeneously distributed over the lamina, in the leaf tissues and cells. The analysis of the variability in leaf growth, and its underlying processes, has recently gained momentum with the development of automated phenotyping platforms that use various technologies to record growth at different scales and at high throughput. These modern tools are likely to accelerate the characterization of gene function and the processes that underlie the control of shoot development. Combined with powerful statistical analyses, trends have emerged that may have been overlooked in low throughput analyses. However, in many examples, the increase in throughput allowed by automated platforms has led to a decrease in the spatial and/or temporal resolution of growth analyses. Concrete examples presented here indicate that simplification of the dynamic leaf system, without consideration of its spatial and temporal context, can lead to important misinterpretations of the growth phenotype. WIREs Dev Biol 2013, 2:809–821. doi: 10.1002/wdev.119


Plant Signaling & Behavior | 2014

Developments at the graft interface in homo- and hetero-grafts: Gene expression and histological changes during the first month after grafting

Maria José Clemente Moreno; Cyril Hevin; Nathalie Ollat; Sarah Jane Cookson

Gene expression changes induced during graft union formation (the first month after grafting) in grapevine have been studied using whole genome microarrays. The genes differentially expressed between the rootstock and graft interface tissues of homo-grafts (Cabernet Sauvignon (CS) grafted onto CS) were compared at 3 and 28 days after grafting (dag). Graft union formation was associated with the upregulation of genes involved in secondary metabolism, cell wall, wound responses and hormone signaling. These gene expression differences were associated with the accumulation of lignin, cellulose and callose in the callus cells. Superimposed upon this, hetero-grafting between two different grapevine genotypes resulted in the further upregulation of stress and/or defense responses at the graft interface. Here we discuss the limitations of the techniques used to study the developments at the graft interface to date and future research directions to understand graft union formation in plants.


New Phytologist | 2006

PHeNOPSIS, an automated platform for reproducible phenotyping of plant responses to soil water deficit in Arabidopsis thaliana permitted the identification of an accession with low sensitivity to soil water deficit

Christine Granier; Luis Aguirrezábal; Karine Chenu; Sarah Jane Cookson; Myriam Dauzat; Philippe Hamard; Jean-Jacques Thioux; Gaëlle Rolland; Sandrine Bouchier-Combaud; Anne Lebaudy; Bertrand Muller; Thierry Simonneau; François Tardieu


Plant Cell and Environment | 2006

Plasticity to soil water deficit in Arabidopsis thaliana: dissection of leaf development into underlying growth dynamic and cellular variables reveals invisible phenotypes

Luis Aguirrezábal; Sandrine Bouchier-Combaud; Amandine Radziejwoski; Myriam Dauzat; Sarah Jane Cookson; Christine Granier


Plant Cell and Environment | 2006

Cell and leaf size plasticity in Arabidopsis: what is the role of endoreduplication?

Sarah Jane Cookson; Amandine Radziejwoski; Christine Granier

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Dive into the Sarah Jane Cookson's collaboration.

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Christine Granier

Institut national de la recherche agronomique

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Nathalie Ollat

Institut national de la recherche agronomique

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Cyril Hevin

Institut national de la recherche agronomique

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Myriam Dauzat

Institut national de la recherche agronomique

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Bertrand Muller

Institut national de la recherche agronomique

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Luis Aguirrezábal

Institut national de la recherche agronomique

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Karine Chenu

University of Queensland

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Amandine Radziejwoski

Institut national de la recherche agronomique

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