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野生大豆转录组测序揭示了低氮胁迫下的基因表达动态。

Transcriptome sequencing of wild soybean revealed gene expression dynamics under low nitrogen stress.

机构信息

Key Laboratory of Agricultural Biological Functional Genes, Northeast Agricultural University, Harbin, 150030, China.

出版信息

J Appl Genet. 2021 Sep;62(3):389-404. doi: 10.1007/s13353-021-00628-1. Epub 2021 Mar 26.

Abstract

Nitrogen is one of the essential elements for plant growth. Wild soybeans (Glycine soja) have strong abilities to survive in harsh and barren environments, and hence become ideal plant model for studying plant adaptability to low nitrogen (LN) conditions. In this study, we analyzed and compared the transcriptomes of wild soybean subjected to LN treatments. We totally identified 1095 (681 up and 414 down) and 5490 (2998 up and 2492 down) differentially expressed genes (DEGs) in the aerial parts (leaf and stem, LS) and roots, respectively. Gene ontology classification analysis revealed that the categories related to LN stress (including oxidation reduction, transcriptional regulation, membrane, and protein phosphorylation) were highly enriched among DEGs. In addition, a total of 784 transcription factor (TF) and 84 transporter protein (TP) genes were determined in LS DEGs, of which some TF genes (NAC1, NAC35, ZFP1, CIM1, and WRKY25) and TP genes like NRT2.5 (nitrate transporter) and ABCC12 (ABC transporter) were widely upregulated under LN stress. Nevertheless, a total of 3859 TF and 370 TP genes were identified in root DEGs, of which some TF genes (NAC6, NAC14, MYB29, MYB92, bZIP62, bZIP72, WRKY60, WRKY58) and TP genes like NRT2.4 and HAK5 (potassium transporter) were upregulated under LN stress. These findings suggest that the identified DEGs may play vital roles in plant responses to LN stress, providing important genetic resources for further functional dissection of plant molecular mechanisms to LN stress.

摘要

氮是植物生长的必需元素之一。野生大豆(Glycine soja)具有在恶劣和贫瘠环境中生存的强大能力,因此成为研究植物适应低氮(LN)条件的理想植物模型。在这项研究中,我们分析和比较了 LN 处理下野生大豆的转录组。我们总共鉴定出地上部分(叶和茎,LS)和根中分别有 1095 个(681 个上调和 414 个下调)和 5490 个(2998 个上调和 2492 个下调)差异表达基因(DEGs)。基因本体分类分析表明,与 LN 胁迫相关的类别(包括氧化还原、转录调控、膜和蛋白磷酸化)在 DEGs 中高度富集。此外,在 LS DEGs 中共确定了 784 个转录因子(TF)和 84 个转运蛋白(TP)基因,其中一些 TF 基因(NAC1、NAC35、ZFP1、CIM1 和 WRKY25)和 TP 基因如 NRT2.5(硝酸盐转运蛋白)和 ABCC12(ABC 转运蛋白)在 LN 胁迫下广泛上调。然而,在根 DEGs 中共鉴定出 3859 个 TF 和 370 个 TP 基因,其中一些 TF 基因(NAC6、NAC14、MYB29、MYB92、bZIP62、bZIP72、WRKY60、WRKY58)和 TP 基因如 NRT2.4 和 HAK5(钾转运蛋白)在 LN 胁迫下上调。这些发现表明,鉴定出的 DEGs 可能在植物对 LN 胁迫的反应中发挥重要作用,为进一步解析植物对 LN 胁迫的分子机制提供了重要的遗传资源。

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