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利用 RNA 测序技术分析大豆(Glycine max)的耐盐性。

RNA sequencing analysis of salt tolerance in soybean (Glycine max).

机构信息

Department of Crop, Soil, and Environmental Sciences, University of Arkansas, Fayetteville, AR 72701, USA; Monsanto Company, 700 Chesterfield Pkwy W, Chesterfield, MO 63017, USA.

Department of Crop, Soil, and Environmental Sciences, University of Arkansas, Fayetteville, AR 72701, USA; Fisher Delta Research Center, University of Missouri, 147 State Hwy T, Portageville, MO 63873, USA.

出版信息

Genomics. 2019 Jul;111(4):629-635. doi: 10.1016/j.ygeno.2018.03.020. Epub 2018 Apr 4.

Abstract

Salt stress causes foliar chlorosis and scorch, plant stunting, and eventually yield reduction in soybean. There are differential responses, namely tolerance (excluder) and intolerance (includer), among soybean germplasm. However, the genetic and physiological mechanisms for salt tolerance is complex and not clear yet. Based on the results from the screening of the RA-452 x Osage mapping population, two F lines with extreme responses, most tolerant and most sensitive, were selected for a time-course gene expression study in which the 250 mM NaCl treatment was initially imposed at the V1 stage and continued for 24 h (hrs). Total RNA was isolated from the leaves harvested at 0, 6, 12, 24 h after the initiation of salt treatment, respectively. The RNA-Seq analysis was conducted to compare the salt tolerant genotype with salt sensitive genotype at each time point using RNA-Seq pipeline method. A total of 2374, 998, 1746, and 630 differentially expressed genes (DEGs) between salt-tolerant line and salt-sensitive line, were found at 0, 6, 12, and 24 h, respectively. The expression patterns of 154 common DEGs among all the time points were investigated, of which, six common DEGs were upregulated and seven common DEGs were downregulated in salt-tolerant line. Moreover, 13 common DEGs were dramatically expressed at all the time points. Based on Log2 (fold change) of expression level of salt-tolerant line to salt-sensitive line and gene annotation, Glyma.02G228100, Glyma.03G226000, Glyma.03G031000, Glyma.03G031400, Glyma.04G180300, Glyma.04G180400, Glyma.05 g204600, Glyma.08G189600, Glyma.13G042200, and Glyma.17G173200, were considered to be the key potential genes involving in the salt-tolerance mechanism in the soybean salt-tolerant line.

摘要

盐胁迫会导致大豆叶片黄化和干枯、植株矮小,最终导致产量降低。大豆种质资源存在差异响应,即耐盐(排除者)和不耐盐(包含者)。然而,盐胁迫的遗传和生理机制很复杂,目前还不清楚。根据 RA-452 x Osage 作图群体的筛选结果,选择了两个极端响应的 F 系,即最耐盐和最敏感的 F 系,进行时间进程基因表达研究,其中在 V1 期开始用 250mM NaCl 处理,并持续 24 小时(hrs)。分别在盐处理开始后 0、6、12、24 小时收获叶片,提取总 RNA。使用 RNA-Seq 分析方法,在每个时间点将耐盐基因型与盐敏感基因型进行比较,进行 RNA-Seq 分析。在 0、6、12 和 24 小时时,分别在耐盐品系和盐敏感品系之间发现了 2374、998、1746 和 630 个差异表达基因(DEGs)。调查了所有时间点的 154 个常见 DEGs 的表达模式,其中 6 个常见 DEGs 在耐盐品系中上调,7 个常见 DEGs 在耐盐品系中下调。此外,13 个常见 DEGs 在所有时间点都有显著表达。基于耐盐品系与盐敏感品系表达水平的 Log2(倍数变化)和基因注释,Glyma.02G228100、Glyma.03G226000、Glyma.03G031000、Glyma.03G031400、Glyma.04G180300、Glyma.04G180400、Glyma.05g204600、Glyma.08G189600、Glyma.13G042200 和 Glyma.17G173200 被认为是大豆耐盐系中参与耐盐机制的关键潜在基因。

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