Kang Byeong Hee, Chowdhury Sreeparna, Kang Se-Hee, Shin Seo-Young, Lee Won-Ho, Lee Hyeon-Seok, Ha Bo-Keun
Department of Applied Plant Science, Chonnam National University, Gwangju 61186, Republic of Korea.
BK21 Interdisciplinary Program in IT-Bio Convergence System, Chonnam National University, Gwangju 61186, Republic of Korea.
Plants (Basel). 2024 Jan 16;13(2):254. doi: 10.3390/plants13020254.
Salt stress is a significant abiotic stress that reduces crop yield and quality globally. In this study, we utilized RNA sequencing (RNA-Seq) to identify differentially expressed genes (DEGs) in response to salt stress induced by gamma-ray irradiation in a salt-tolerant soybean mutant. The total RNA library samples were obtained from the salt-sensitive soybean cultivar Kwangan and the salt-tolerant mutant KA-1285. Samples were taken at three time points (0, 24, and 72 h) from two tissues (leaves and roots) under 200 mM NaCl. A total of 967,719,358 clean reads were generated using the Illumina NovaSeq 6000 platform, and 94.48% of these reads were mapped to 56,044 gene models of the soybean reference genome (Glycine_max_Wm82.a2.v1). The DEGs with expression values were compared at each time point within each tissue between the two soybeans. As a result, 296 DEGs were identified in the leaves, while 170 DEGs were identified in the roots. In the case of the leaves, eight DEGs were related to the phenylpropanoid biosynthesis pathway; however, in the roots, within , a major QTL associated with salt tolerance in soybean plants, was differentially expressed. Overall, these differences may explain the mechanisms through which mutants exhibit enhanced tolerance to salt stress, and they may provide a basic understanding of salt tolerance in soybean plants.
盐胁迫是一种严重的非生物胁迫,在全球范围内降低了作物的产量和品质。在本研究中,我们利用RNA测序(RNA-Seq)来鉴定耐盐大豆突变体中响应γ射线辐照诱导的盐胁迫的差异表达基因(DEG)。总RNA文库样本取自盐敏感大豆品种光安和耐盐突变体KA-1285。在200 mM NaCl条件下,从两个组织(叶片和根)的三个时间点(0、24和72小时)采集样本。使用Illumina NovaSeq 6000平台共生成了967,719,358条clean reads,其中94.48%的reads被映射到大豆参考基因组(Glycine_max_Wm82.a2.v1)的56,044个基因模型上。比较了两个大豆品种每个组织内每个时间点具有表达值的DEG。结果,在叶片中鉴定出296个DEG,而在根中鉴定出170个DEG。在叶片中,8个DEG与苯丙烷生物合成途径相关;然而,在根中,大豆植株中与耐盐性相关的一个主要QTL被差异表达。总体而言,这些差异可能解释了突变体表现出增强的耐盐胁迫能力的机制,并且它们可能提供对大豆植株耐盐性的基本理解。