Root transcriptome analysis of Saccharum spontaneum uncovers key genes and pathways in response to low-temperature stress

•First time-course root transcriptomes of wild sugarcane challenged with cold stress.•4425 Unigenes differentially expressed under cold stress.•Several transcription factors, stress responsive genes and pathways were involved.•Phenylpropanoid and galactose pathways most significantly upregulated in...

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Published inEnvironmental and experimental botany Vol. 171; p. 103935
Main Authors Dharshini, S., Hoang, Nam V., Mahadevaiah, C., Sarath Padmanabhan, T.S., Alagarasan, G., Suresha, G.S., Kumar, Ravinder, Meena, Mintu Ram, Ram, Bakshi, Appunu, C.
Format Journal Article
LanguageEnglish
Published Elsevier B.V 01.03.2020
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Summary:•First time-course root transcriptomes of wild sugarcane challenged with cold stress.•4425 Unigenes differentially expressed under cold stress.•Several transcription factors, stress responsive genes and pathways were involved.•Phenylpropanoid and galactose pathways most significantly upregulated in long-term.•A useful resource for developing climate-resilient sugarcane varieties. Low-temperature (LT) stress is known to restrain sugarcane productivity in sub-tropical regions significantly. Many researchers have prioritized their work towards developing climate-resilient sugarcane varieties incorporating genome of stress-tolerant sugarcane related wild-type species in the pre-breeding programs. However, the lack of genomic resources for wild-type sugarcane limits the identification and utilization of stress-related genes in molecular breeding. In this study, for the first time, we generated ∼182 million RNA-seq paired-end reads for Saccharum spontaneum roots grown under low temperature (10 °C) at different time intervals (0 h, 3 h, 6 h, 12 h, 24 h, and 48 h), to identify LT stress responsive genes and pathways. These data were assembled into 141,409 unigenes and subsequently used to identify 2715 upregulated and 1710 downregulated transcripts under LT stress. Combining evidences from GO enrichment, KEGG pathways, histological studies, biochemical assays, and physiological analysis, our results revealed several key genes and pathways involved in cold acclimatization in the S. spontaneum roots. Transcription profiling of roots during LT stress revealed cold stress sensors (i.e., proline, MDA, calcium-dependent kinase, G-coupled proteins, and histidine kinase) that trigger and activate signal transduction through transcription factors (i.e., MYB, ERF, ARF2, DREB, CAMTA, and C2H2) resulting in upregulation of LT stress responsive genes (i.e, annexin, LEA, germins, LT dehydrins, osmotins, and COR) thereby enhancing cold tolerance. Also, transcriptomic analysis envisaged cold responsive metabolic pathways such as phenylpropanoid and sugar metabolism stimulate the synthesis of flavonoid, sucrose, galactose, raffinose, and fructose, antioxidants, phytohormones, and secondary metabolites, and thus trigger cold-responsive transcriptional regulation. Together, this study provides insights into cold tolerance of wild sugarcane roots to LT stress, thus providing a foundation for developing climate-resilient sugarcane varieties.
ISSN:0098-8472
1873-7307
DOI:10.1016/j.envexpbot.2019.103935