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Rice (Oryza sativa. L) genetic diversity for early vigor and drought ...

Rice (Oryza sativa. L) genetic diversity for early vigor and drought ...

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Introductionestimation. The identification of relevant process based traits <strong>for</strong> <strong>genetic</strong> studies was thus a majorchallenge during the last decades <strong>for</strong> ecophysiologists (Dingkuhn et al. 2006; Tardieu et al. 2010).Recently some approaches proved their relevance <strong>for</strong> phenotyping process based traits on a largenumber of genotypes. This is the case of high throughput imaging methods that enable a rapidcharacterization of plant growth dynamics or water status (Berger et al. 2010). The application ofmodeling also showed its relevance to phenotype process based traits using the parameters ofequations <strong>for</strong>malizing plant response to environmental variables to differentiate genotypes; suchparameters are thus genotypic <strong>and</strong> less prone to GxE than corresponding measured variables(Dingkuhn et al. 2006; Tardieu et al. 2010). This was pioneered by Reymond et al. (2004) using asimple model (with 3 equations) predicting maize leaf expansion rate (LER) response toenvironmental variables related to <strong>drought</strong> conditions (leaf temperature, vapor pressure deficit <strong>and</strong>soil water potential). Indeed consistent associations of Quantitative Trait Loci (QTL) <strong>and</strong> modelparameters were reported <strong>for</strong> hundreds of genotypes in maize populations with different <strong>genetic</strong>backgrounds <strong>and</strong> across environments (Welcker et al. 2011).The interest of metabolomics <strong>for</strong> plant phenotyping has been less explored (Fernie et al. 2009),although they might reveal genotypic variation <strong>for</strong> growth <strong>and</strong> adaptation strategies (Stitt et al. 2010)or <strong>for</strong> physiological traits (Ishimaru et al. 2007). The role of non structural carbohydrates (NSC) asmarkers of genotypic growth pattern was demonstrated: on Arabidopsis, Sulpice et al. (2009)reported a negative correlation between seedling growth <strong>and</strong> starch accumulation <strong>and</strong> on Medicagotrucatula V<strong>and</strong>ecasteele et al. (2011) reported a negative correlation between seedling <strong>vigor</strong> <strong>and</strong>sucrose:rafinose ratio. Meanwhile in a preliminary study on 200 rice <strong>sativa</strong> genotypes grown underwell watered conditions Luquet et al. (2008b) reported that <strong>early</strong> <strong>vigor</strong> was associated to low NSCconcentration in the plant. Metabolic component traits demonstrated also their interest todiscriminate genotypes <strong>for</strong> <strong>drought</strong> response mechanisms (Shao et al. 2009; Verslues et al. 2011),rice vegetative growth (Cabuslay et al. 2002). This suggests the relevance of exploring the <strong>genetic</strong><strong>diversity</strong> <strong>for</strong> NSC during rice vegetative growth.OBJECTIVES, OVERVIEW OF THE CHAPTERS AND THE METHODOLOGYWithin Genphen <strong>and</strong> Orytage projects, extensive phenotypic data sets were generated with athreefold purpose (i) identify traits contributing to rice growth <strong>and</strong> adaptation strategies (to <strong>drought</strong>in particular) <strong>and</strong> their <strong>diversity</strong>, (ii) characterize physiological <strong>and</strong>/or <strong>genetic</strong> linkages among traits,<strong>and</strong> their GxE; <strong>and</strong> (iii) detect QTLs <strong>and</strong> related favorable alleles <strong>for</strong> studied traits using a chip ofabout 1 million SNP markers <strong>for</strong> association <strong>genetic</strong>s studies. Genetic studies are planned <strong>for</strong> June2012 when the chip of SNPs markers will be available.17

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