Institute of Forage and Grassland Sciences, Heilongjiang Academy of Agricultural Sciences, Harbin 150086, China.
Institute of Industrial Crop, Heilongjiang Academy of Agricultural Sciences, Harbin 150086, China.
Int J Mol Sci. 2019 Jan 16;20(2):369. doi: 10.3390/ijms20020369.
Flax ( L.) is an important industrial crop that is often cultivated on marginal lands, where salt stress negatively affects yield and quality. High-throughput RNA sequencing (RNA-seq) using the powerful Illumina platform was employed for transcript analysis and gene discovery to reveal flax response mechanisms to salt stress. After cDNA libraries were constructed from flax exposed to water (negative control) or salt (100 mM NaCl) for 12 h, 24 h or 48 h, transcription expression profiles and cDNA sequences representing expressed mRNA were obtained. A total of 431,808,502 clean reads were assembled to form 75,961 unigenes. After ruling out short-length and low-quality sequences, 33,774 differentially expressed unigenes (DEUs) were identified between salt-stressed and unstressed control (C) flax. Of these DEUs, 3669, 8882 and 21,223 unigenes were obtained from flax exposed to salt for 12 h (N1), 24 h (N2) and 48 h (N4), respectively. Gene function classification and pathway assignments of 2842 DEUs were obtained by comparing unigene sequences to information within public data repositories. qRT-PCR of selected DEUs was used to validate flax cDNA libraries generated for various durations of salt exposure. Based on transcriptome sequences, 1777 EST-SSRs were identified of which trinucleotide and dinucleotide repeat microsatellite motifs were most abundant. The flax DEUs and EST-SSRs identified here will serve as a powerful resource to better understand flax response mechanisms to salt exposure for development of more salt-tolerant varieties of flax.
亚麻(Linum usitatissimum)是一种重要的工业作物,通常在边缘土地上种植,而盐分胁迫会对其产量和品质产生负面影响。本研究采用高通量 RNA 测序(RNA-seq)技术,利用强大的 Illumina 平台进行转录分析和基因发现,以揭示亚麻对盐胁迫的响应机制。构建了暴露于水(阴性对照)或盐(100 mM NaCl) 12 h、24 h 和 48 h 的亚麻 cDNA 文库后,获得了转录表达谱和代表表达 mRNA 的 cDNA 序列。共组装了 431,808,502 条清洁读数,形成了 75,961 个非冗余基因。排除短序列和低质量序列后,在盐胁迫和对照(C)亚麻之间鉴定出 33,774 个差异表达基因(DEU)。其中,12 h(N1)、24 h(N2)和 48 h(N4)盐暴露的亚麻分别获得了 3669、8882 和 21,223 个 DEU。通过将 unigene 序列与公共数据库中的信息进行比较,获得了 2842 个 DEU 的基因功能分类和途径分配。对不同盐暴露时间生成的亚麻 cDNA 文库进行了所选 DEU 的 qRT-PCR 验证。基于转录组序列,鉴定出 1777 个 EST-SSRs,其中三核苷酸和二核苷酸重复微卫星基序最为丰富。本研究鉴定的亚麻 DEU 和 EST-SSRs 将成为更好地理解亚麻对盐暴露响应机制的有力资源,有助于开发更耐盐的亚麻品种。