Abstract
Background - Sugarcane (Saccharum spp hybrid), an important C4 perennial plantation crop, globally grown for white sugar and ethanol production. Red rot caused by Colletotrichum falcatum is one of the most important threats affecting sugarcane productivity in many countries including India.Materials and Methods - Comprehensive understanding is very much needed to define their transcription level differences and their key regulatory genes during interaction of sugarcane with C. falcatum. To compute and evaluate the molecular mechanism in sugarcane, transcriptome analysis of sugarcane challenged with C. falcatum was sequenced using Hi-Seq 2500 and gene expression profiles were generated by qRT-PCR assays in both compatible and incompatible interactions after challenge inoculation of C. falcatum in sugarcane.Results - A total of 15,728,914 reads were aligned to 48,935 unigenes using BOWTIE 2; the unigenes were annotated using BLASTX and found that 39,895 unigenes were annotated and 22,025 were unigenes with respect to host species, 8,830 with respect to Colletotrichum spp and 9,040 were found to be novel genes. A total of 243 transcription factors (TFs) were found to be predicted in sugarcane challenged with C. falcatum and those TFs were divided into 45 specific families. WRKY, MYB, NAC, bHLH and AUX/IAA transcription factors were found to be abundant which are considered to be key regulators in controlling wide range of molecular events such as defense response, oxidative stimuli, host signalling and triggering disease resistance. In addition, a lot of stress related genes and genes involved in gene ontological and KEGG pathway were significantly affected due to C. falcatum infection. Quantative real time PCR assays carried out to validate reliability of observed expression patterns in sugarcane in response to C. falcatum infection illustrates first transcriptome wide in planta identification and analysis of TF repertoire in the host pathogen interaction.Conclusion - The results of this study provide a benchmark discovery in finding host targets and provide tissue specific data set of genes that express in response to C. falcatum in sugarcane and also a complete analysis of main group of genes that significantly enriched under this condition. This is the first comprehensive work provides basis for the further studies to dissect role of TFs at molecular level in sugarcane defense to fungal pathogens.