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首页> 外文期刊>Journal of radiation research >Transcriptome sequencing reveals hotspot mutation regions and dwarfing mechanisms in wheat mutants induced by γ-ray irradiation and EMS
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Transcriptome sequencing reveals hotspot mutation regions and dwarfing mechanisms in wheat mutants induced by γ-ray irradiation and EMS

机译:转录组测序显示由γ射线照射和EMS诱导的小麦突变体中的热点突变区域和矮化机制

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Induced mutation is an important approach for creating novel plant germplasms. The introduction of dwarf or semi-dwarf genes into wheat has led to great advancements in yield improvement. In this study, four elite dwarf wheat mutants, named dm1–dm4, induced from γ-ray irradiation or ethyl methanesulfonate (EMS) mutagenesis, were used to identify transcriptome variations and dwarfing mechanisms. The results showed that the hotspot regions of mutations distributed on the chromosomes were consistent among the four mutant lines and these regions were mainly located around the 50, 360 and 400?Mb positions of chromosome 1A and the distal regions of chromosomes 2A and 2BL. Kyoto Encyclopedia of Genes and Genomes (KEGG) analyses suggested that ‘protein processing in endoplasmic reticulum’ was the most common significantly enriched pathway based on the differentially expressed genes (DEGs) between wildtype (WT) and the mutants. Notably, 18 out of 20 genes involved in this process encode heat shock proteins (HSPs). The results implied that HSPs might participate in wheat dwarfism response and function in the dwarfism process through protein folding and/or degradation. Moreover, seven genes in dm4 involved in modulating auxin levels were down-regulated and dm4 was more sensitive to auxin treatment compared with WT, indicating the important roles of auxin in regulation of dwarf phenotype in dm4. This study not only identified transcriptome sequence variation induced by physical and chemical mutagenesis but also revealed potential dwarfing mechanisms in the wheat mutant lines.
机译:诱导突变是制造新型植物种质的重要方法。侏儒或半侏儒基因进入小麦的引入导致了产量改善的巨大进步。在该研究中,使用由γ射线照射或甲磺酸乙酯(EMS)诱变的诱导的DM1-DM4的四个Elite矮小的小麦突变体进行鉴定转录组变异和矮化机制。结果表明,分布在染色体上的突变的热点区域在四种突变线中是一致的,这些区域主要位于50,360和400〜400〜2a和2b的远端区域围绕50,360和400?Mb位置。染色体2a和2bl的远端区域。基因和基因组(Kegg)的京都百科全书(Kegg)分析表明,“内质网的蛋白质加工”是基于野生型(WT)和突变体之间的差异表达基因(DEGS)最常见的富集途径。值得注意的是,该过程中涉及20个基因中的18个编码热休克蛋白(HSP)。结果暗示,HSP可能通过蛋白质折叠和/或降解参与矮化过程中的小麦矮主义反应和功能。此外,与WT相比,DM4涉及调节植物素水平的DM4中的七种基因,与生长素治疗更敏感,表明植物蛋白在DWARF表型调节中的重要作用。该研究不仅鉴定了物理和化学诱变诱导的转录组序列变异,而且还揭示了小麦突变体中的潜在矮化机制。

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