ABSTRACT
A differential expression study on the Saccharum spp.-Sporisorium scitamineum pathogenic interaction was carried out in the susceptible Ja60-5 and the resistant M31/45 genotypes. Using cDNA-AFLP analysis, a total of 64 transcript-derived fragments (TDFs) was found to be differentially expressed, with the majority (67.2%) of the differential TDFs up-regulated in the resistant M31/45 cultivar. The plant response against S. scitamineum infection was complex, representing major genes involved in oxidative burst, defensive response, ethylene and auxins pathways during the first 72 h post-inoculation. Results obtained suggest a key role for genes involved in the oxidative burst and the lignin pathways in the initial sugarcane defense against the S. scitamineum infection.
Subject(s)
DNA, Plant/genetics , Gene Expression Regulation, Plant , Host-Pathogen Interactions , Saccharum/genetics , Saccharum/microbiology , Ustilaginales/physiology , Amplified Fragment Length Polymorphism Analysis , DNA, Complementary/genetics , Ethylenes/metabolism , Gene Expression Profiling , Indoleacetic Acids/metabolism , Lignin/metabolism , Oxidation-Reduction , Plant Diseases/genetics , Saccharum/metabolismABSTRACT
We describe the procedures for recovering transgenic sugarcane from co-cultivation of both calli and in vitro plants with Agrobacterium tumefaciens. The correct tissue culture strategies and the use of super-binary vector or super-virulent strain are crucial for the successful sugarcane transformation. Both plant regeneration via calli culture and micropropagation strategies can be optimized to a wide spectrum of sugarcane genotypes, thus the procedures presented here could be applied to genetic engineering of Saccharum spp. after minor modifications. For the case of sugarcane transformation using in vitro plants, four selective micropropagation steps must be sufficient to eliminate chimera plants.
