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- W4384156730 abstract "Trichoderma has been recognized as a beneficial fungus to promote crop growth and resistance against pathogens in plants. However, our understanding about the underling molecular mechanism is limited. Delineating the plant's responses to Trichoderma colonization is crucial to understand the molecular basis of their interaction. Therefore, to detect the key differentially expressed genes (DEGs), a pairwise transcriptome analysis was carried at 48 h post inoculation (hpi) between control and Trichoderma-treated roots of castor (Ricinus communis L.). A total of 20,696 plant transcripts were detected using EdgeR software, of which 1508 were DEGs. 474 of these putative DEGs were upregulated while the remaining were downregulated (p < 0.05) in the root samples of the castor genotype, DCS107 treated with Trichoderma asperellum strain 1736. Majority of the DEGs that were downregulated were related to stress, hypersensitive response, reactive oxygen species (ROS), phenylpropanoid pathway, secondary metabolite biosynthesis, carbohydrate and amino acid biosynthesis/metabolism, ABC transporters and transcription factors accompanied by proteins involved in electron transport. Further, to confirm the findings, Real Time-quantitative Polymerase Chain Reaction (RT-qPCR) was carried at 12, 24 and 48 hpi for a set of 9 DEGs with a putative role in stress and defense responses. 5 of these genes involved in stress response were found to be downregulated, similar to the transcriptome result. Likewise, the expression of the remaining genes- WRKY71, RPV, ZAT5 and RPS2 with a function in defense were found to be upregulated suggesting that these genes might be playing a crucial role in Trichoderma-mediated responses in castor." @default.
- W4384156730 created "2023-07-14" @default.
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- W4384156730 date "2023-09-01" @default.
- W4384156730 modified "2023-09-27" @default.
- W4384156730 title "Delineating host responses induced by Trichoderma in castor through comparative transcriptome analysis" @default.
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- W4384156730 doi "https://doi.org/10.1016/j.rhisph.2023.100745" @default.
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