Isolation, characterization and expression analysis of novel water deficit stress-responsive DEEPER ROOTING 1 (DRO1) gene from drought-tolerant Erianthus arundinaceus

P. Swathik Clarancia, M. Naveenarani, R. Valarmathi, G. Suresha, G. Hemaprabha, B. Ram, C. Appunu
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引用次数: 1

Abstract

Sugarcane ( Saccharum spp.) is an important food, fodder and energy crop in India. Its production and productivity are mainly constrained due to water deficit stress during different growth stages. Of the root system architecture traits, deep rooting helps plants to avoid drought-induced stress by foraging moisture from deeper layers of soil. Hence, in this study, a novel drought-responsive DEEPER ROOTING 1 ( DRO1 ) gene cloned from drought-tolerant Erianthus arundinaceus was characterized. The open reading frame of this gene is 765 bp that encodes for a single polypeptide of 254 amino acids. In silico analysis of DRO1 protein using bioinformatics tools revealed its size of 28.91 kDa with theoretical pI 5.39, instability index 67.57, aliphatic index 69.92 and GRAVY of -0.86. Subcellular localization by LocTree3 tool suggested that DRO1 protein expression is localized in the nucleus. The phylogenetic tree exhibited that DRO1 from Erianthus arundinaceus is closely associated with that of Sorghum bicolor and Triticum aestivum. Protein interaction network analysis showed DRO1 association with WOX11, which promotes the development of crown roots and ARL1 (Adventitious rootless1) required for adventitious root formation. Quantitative gene expression analysis indicated that the DRO1 gene is differentially upregulated in root tissue of E. arundinaceus and Saccharum spp. commercial hybrid under water deficit stress conditions. EaDRO1 gene can be a novel source for developing drought stress tolerant genotypes through genetic engineering approach.
耐旱性Erianthus arundinaceus中新的水分亏缺胁迫响应基因deep生根1 (DRO1)的分离、表征和表达分析
甘蔗是印度重要的粮食、饲料和能源作物。其生产和生产力主要受到不同生长阶段缺水胁迫的制约。在根系结构特征中,深根有助于植物通过从更深的土壤层获取水分来避免干旱引起的压力。因此,在本研究中,从耐旱的海南花中克隆了一个新的抗旱性DEPER ROOTING 1(DRO1)基因。该基因的开放阅读框为765bp,编码254个氨基酸的单个多肽。使用生物信息学工具对DRO1蛋白进行的计算机分析显示,其大小为28.91kDa,理论pI为5.39,不稳定性指数为67.57,脂族指数为69.92,GRAVY为-0.86。LocTree3工具的亚细胞定位表明DRO1蛋白的表达定位在细胞核中。系统发育树分析表明,芒花DRO1与双色高粱和普通小麦DRO1密切相关。蛋白质相互作用网络分析显示DRO1与WOX11结合,WOX11促进不定根形成所需的冠根和ARL1(不定根1)的发育。定量基因表达分析表明,在缺水胁迫条件下,DRO1基因在E.arundinaceus和Saccharum spp.商业杂交种的根组织中差异上调。EaDRO1基因是通过基因工程方法开发耐旱基因型的新来源。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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