Document Type : Original Article
Authors
1 Department of biotechnology and plant breeding, Science and Research Branch, Islamic Azad University, Tehran, Iran
2 Life Science Engineering, Faculty of New Sciences and Technologies, University of Tehran, Iran
3 Department of Plant Molecular Biotechnology, National Research Institute of Genetic Engineering and Biotechnology
Abstract
Introduction
In order to identify cold tolerant cultivars in sugarcane, in December 2015 and one week after the occurrence of -1.2 °C, by morphological study of 454 sugarcane cultivars, the reaction of these cultivars and their tolerance to cold were investigated.
Materials and methods
In the first stage of the experiment (morphology), 54 cultivars were introduced as resistant and tolerant cultivars and 400 cultivars were introduced as cold and very sensitive cultivars. In 2016, to evaluate cultivars based on biochemical indices, out of 54 resistant cultivars, 5 cultivars, and out of 400 susceptible cultivars, 5 cultivars were selected and the amount of free amino acids, Proline and Malondialdehyde, in them before and after the onset of cold, it was measured. Among the selected cultivars of the previous stage, BR00-01 cultivar was selected as the most tolerant cultivar, and TUC66-107 cultivar as the most sensitive cultivar to cold, to apply cold stress in the cold storage and continue the project in the molecular stage. After planting them in plastic pots, leaf sampling was performed in the refrigeration under stress and to extract TotalRNA. After RNA extraction, the quantity and quality of RNA samples were measured. Using the Illumina Hiseq250 platform in the RNAseq technique, after confirming the quantity and quality of the extracted RNAs, the TruSeq cDNA library was constructed by the Chinese company Novogene and sequencing for RNAseq was done as a pair-end with a length of 150 nucleotides. After sequencing, the data were downloaded in compressed files in Fastq format from the Novogene website. The quality of the raw reads was checked using FastQC software. Trimmomatic software was used in the trimming step. After aligning the reads to the sugarcane reference genome, quantified reads were normalized, differential expression analysis was performed, and genes with differential expression were analyzed and pathways were mapped. After analyzing the differential expression of genes and obtaining the values, GO enrichment analysis was performed to classify the genes based on the placement of their products. Next, the path analysis was performed using the kobas database. Then, in order to enrich the pathways, significant pathways were identified with Corrected P-Value <0.05 for genes with increased and decreased expression.
Results and discussion
he results of differential expression of genes showed that out of a total of 62285 expressed genes, 12674 genes have differential expression in different comparisons between treatments, of which 6939 genes decreased expression and 5735 genes increased expression. After enriching the pathways, genes that could be 95% probable in 18 treatment comparisons to attribute their change in expression to cold stress were identified, and marker genes were identified in these comparisons. According to the results of the metabolic study, increasing the concentration of free amino acids, Proline and Malondialdehyde increased the plant's tolerance to cold. In this study, due to cold stress, various biosynthetic and metabolic pathways were activated under the influence of the activity of genes controlling these pathways to produce their products. These pathways include the biosynthesis of the amino acids arginine and Proline, the biosynthesis of Phenylpropanoid, the riboflavin metabolism, and the MAPK messenger pathway, in which the genes involved increased expression during cold stress. Meanwhile, the PR1 gene was detected in the MAPK messenger pathway, which showed an increase in expression with decreasing temperature Increased expression of genes in MAPK, Phenylpropanoid, sulfur, Glycerophospholipid, arachidonic acid, lipid ether, riboflavin and Proline signaling pathways indicates that the products of some genes controlling these pathways play a role in increasing cold tolerance of sugarcane.
Conclusions
The results of morphological, metabolic and molecular studies showed that there is a correlation between these indices and their values in resistant cultivar. When screening sugarcane clones for cold, the best clones can be selected by measuring the amount of secondary metabolites. In this study, genes affecting cell physiology pathways were identified and their role in increasing sugarcane tolerance to cold was elucidated. Using these genes, you can use them in a sugarcane breeding program to screen for cold-resistant clones. In the sugarcane breeding program, these genes can be used as markers in the screening of clones.
Keywords
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