Tative real-time PCR; RLCK: receptor like cytoplasmic kinases; TAG: triacylglycerol; WebMeV: numerous experiment viewerAvailability of data and supplies The RNA-seq information have already been submitted to NCBI and can be accessed via the following link: https://www.ncbi.nlm.nih.gov/sra/PRJNADeclarationsEthics approval and consent to participate All approaches were performed in accordance with the relevant recommendations, regulations and institutional recommendations. Consent for publication Not applicable. Competing interests The authors declare that they have no competing interests. Author particulars 1 Department of Botany and Plant Pathology, Purdue University, West Lafayette, IN 47907, USA. 2Department of RORγ Purity & Documentation Horticulture and Landscape Architecture, Purdue University, West Lafayette, IN 47907, USA. Received: three February 2021 Accepted: 22 MarchSupplementary InformationThe on-line version includes supplementary material readily available at https://doi. org/10.1186/s12864-021-07609-y. Extra file 1 Fig. S1. Gene Ontology enrichment evaluation of DEGs in between RTx2911 and RTx430 at 24 hpi. Enriched GO biological course of action for up (a) and down (b) regulated genes at 24 hpi in RTx2911 compared to RTx430. Further file 2 Fig. S2. Gene Ontology enrichment analysis of DEGs between RTx2911 and RTx430 at 24 hpi. a Enriched GO molecular method of up-regulated genes at 24 hpi in RTx2911 in Enolase MedChemExpress comparison to RTx430. b Enriched GO molecular course of action of down-regulated genes at 24 hpi in RTx2911 in comparison to RTx430. Added file three Fig. S3. Enriched GO biological processes among 0 and 24 hpi for RTx2911 and RTx430. a Up-regulated genes at 24 hpi in RTx2911 when compared with 0 hpi. b Up-regulated genes at 24 hpi in RTx430 compared to 0 hpi. c Down-regulated genes at 24 hpi in RTx2911 in comparison to 0 hpi. d Down-regulated genes at 24 hpi in RTx2911 when compared with 0 hpi. Further file four Table S1. Genes differentially expressed in between genotypes at 0 hpi Additional file five Table S2. Genes differentially expressed amongst genotypes at 24 hpi Extra file six Table S3. Enriched GO molecular course of action for genes differentially expressed involving genotypes: list and description of protein kinase genes up regulated in RTx2911 at 24 hpi Added file 7 Table S4. Genes differentially expressed in between 0 and 24 hpi in RTx2911 Further file eight Table S5. Genes differentially expressed among 0 and 24 hpi in RTx430 Added file 9 Table S6. List of primers used for qRT-PCR Extra file 10. Facts from the workflow and python scripts utilized to conduct differential gene expression analysis Acknowledgements NA Authors’ contributions HN conceived the project, performed the experiments and wrote the paper. SL performed the experiments. YL, generated suggestions, helped with information analysis and wrote the paper. TM conceived the project idea, directed the project, generated experimental concepts and wrote the paper. The author(s) read and approved the final manuscript. Funding This study was created achievable by means of funding by the Feed the Future Innovation Lab for Collaborative Investigation on Sorghum and Millet by means of grants from American Folks supplied to the United states Agency for International Improvement (USAID) beneath cooperative agreement No. AIDOAA-A-13-00047. The contents are the sole duty of your authors and don’t necessarily reflect the views of USAID or the United states Government. Sanghun Lee was supported by the Next-Generation BioGreen 21 Plan (SSAC, Project No. PJ01317302), Rural Improvement Administration,.