Key Laboratory of Plant Stress Biology, State Key Laboratory of Cotton Biology, School of Life Sciences, Henan University, Kaifeng 475001, China.
College of Agriculture, Nanjing Agricultural University, Nanjing 210095, China.
Int J Mol Sci. 2020 May 19;21(10):3595. doi: 10.3390/ijms21103595.
As the diploid progenitor of common wheat, is considered to be a valuable resistance source to various biotic and abiotic stresses. However, little has been reported concerning the molecular mechanism of drought tolerance in . In this work, the drought tolerance of 155 Ae. tauschii accessions was firstly screened on the basis of their coleoptile lengths under simulated drought stress. Subsequently, two accessions (XJ002 and XJ098) with contrasting coleoptile lengths were selected and intensively analyzed on rate of water loss (RWL) as well as physiological characters, confirming the difference in drought tolerance at the seedling stage. Further, RNA-seq was utilized for global transcriptome profiling of the two accessions seedling leaves under drought stress conditions. A total of 6969 differentially expressed genes (DEGs) associated with drought tolerance were identified, and their functional annotations demonstrated that the stress response was mediated by pathways involving alpha-linolenic acid metabolism, starch and sucrose metabolism, peroxisome, mitogen-activated protein kinase (MAPK) signaling, carbon fixation in photosynthetic organisms, and glycerophospholipid metabolism. In addition, DEGs with obvious differences between the two accessions were intensively analyzed, indicating that the expression level of DEGs was basically in alignment with the physiological changes of under drought stress. The results not only shed fundamental light on the regulatory process of drought tolerance in , but also provide a new gene resource for improving the drought tolerance of common wheat.
作为普通小麦的二倍体祖先, 被认为是各种生物和非生物胁迫的宝贵抗性来源。然而,关于 在干旱耐受方面的分子机制却鲜有报道。在这项工作中,首先基于模拟干旱胁迫下的胚芽鞘长度对 155 个 Ae. tauschii 材料进行了耐旱性筛选。随后,选择了两个胚芽鞘长度差异较大的材料(XJ002 和 XJ098)进行深入分析,包括失水率(RWL)以及生理特性,从而确认了幼苗期耐旱性的差异。进一步,利用 RNA-seq 对两个材料在干旱胁迫条件下的幼苗叶片进行了全转录组分析。共鉴定出 6969 个与耐旱性相关的差异表达基因(DEGs),其功能注释表明,胁迫反应是通过涉及α-亚麻酸代谢、淀粉和蔗糖代谢、过氧化物酶体、丝裂原激活蛋白激酶(MAPK)信号转导、光合生物中的碳固定和甘油磷脂代谢等途径来介导的。此外,对两个材料间存在明显差异的 DEGs 进行了深入分析,表明 DEGs 的表达水平与 在干旱胁迫下的生理变化基本一致。这些结果不仅为阐明 在耐旱性调控过程提供了基础,也为改良普通小麦的耐旱性提供了新的基因资源。