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                <term xml:lang="en">MONOLIGNOL</term>
                <term xml:lang="en">FERULIC ACID</term>
                <term xml:lang="en">ARABINOXYLANS</term>
                <term xml:lang="en">DIGESTIBILITY</term>
                <term xml:lang="en">LIGNIN</term>
                <term xml:lang="en">BIOETHANOL</term>
                <term xml:lang="en">BIOFUEL</term>
                <term xml:lang="en">CELL WALL</term>
                <term xml:lang="en">MAIZE</term>
                <term xml:lang="en">CATTLE FEEDING</term>
                <term xml:lang="en">DEGRADABILITY</term>
                <term xml:lang="en">GENETIC RESOURCES</term>
                <term xml:lang="en">GENETIC ENGINEERING</term>
                <term xml:lang="en">PLANT BREEDING</term>
                <term xml:lang="en">DROUGHT TOLERANCE</term>
                <term xml:lang="en">INTAKE</term>
                <term xml:lang="fr">AMELIORATION DES PLANTES</term>
                <term xml:lang="fr">BIOTECHNOLOGIE</term>
                <term xml:lang="fr">CELLULOSE</term>
                <term xml:lang="fr">P-COUMARIC ACID</term>
                <term xml:lang="fr">SILAGE</term>
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            <abstract xml:lang="en">
              <p>Silage maize is Currently, with grazing, the basis of cattle feeding. In the near future, maize stover and cereal straws will also be a major Source of carbohydrates for sustainable biofuel production. The embedding of cell wall in lignins and the linkages between lignins, p-hydroxycinnamic acids, and arabinoxylans greatly influences cell wall properties, including the enzymatic degradability of structural polysaccharides in animal rumen or industrial fermenters. Breeding for higher silage quality and biofuel production will thus be based on the discovery of genetic traits involved in each component biosynthesis and deposition in each lignified tissue. Genes involved or putatively involved in the biosynthesis of the grass cell wall were searched for, including phenolic Compounds, cell wall carbohydrates and regulation factors. While most cytosolic steps of monolignol biosynthesis have been identified, most of lignin pathway genes belong to small multigene families which were all identified based on data available in the Maize Genomics Sequencing Project (MGSP) database. Cell wall carbohydrate genes were identified based on their Arabidopsis orthologs and previous research in C3 grasses by MITCHELL et al. (2007). Transcription and regulation factors of cell wall genes were similarly identified based their orthologs described both in Arabidopsis and woody species. All these genes were mapped in silico considering their physical position in the MGSP database. Physical positions of previously described QTL for cell wall degradability, lignin and p-hydroxycinnamic acid contents were also searched for based on the position of the flanking market in the MGSP database and distances between QTL and flanking markets. While only a few lignin pathway genes mapped to QTL positions, several colocalizations were shown between QTL and transcription factor physical positions. This last result is in agreement with expression Studies which highlighted that several genes in the lignin pathway are simultaneously under-expressed in lines with higher cell wall degradability, likely corroborating an upstream regulation rather than co-regulation phenomena. However, none of these possible candidate genes have yet been validated and many QTL still do not have relevant candidates. A lot of relevant candidate genes are still to be discovered among those involved in lignin pathway gene regulation, in regulation of lignified tissue assembly, and in cell wall carbohydrate biosynthesis and deposition. In addition, in spite of their critical involvement in maize cell wall assembly and degradability, genes involved in ferulic acid biosynthesis and linkages with other cell wall components are little known.</p>
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