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Transcriptome analysis of nitrogen-starvation-responsive genes in rice

机译:水稻氮饥饿响应基因的转录组分析

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Background Nitrogen (N), a critical macronutrient for plant growth and development, is a major limiting factor in most agricultural systems. Microarray analyses have been conducted to investigate genome-wide gene expression in response to changes in N concentrations. Although RNA-Seq analysis can provide a more precise determination of transcript levels, it has not previously been employed to investigate the expression of N-starvation-induced genes. Results We constructed cDNA libraries from leaf sheaths and roots of rice plants grown under N-deficient or -sufficient conditions for 12?h. Sequencing the libraries resulted in identification of 33,782 annotated genes. A comparison of abundances revealed 1,650 transcripts that were differentially expressed (fold-change?≥?2) due to an N-deficiency. Among them, 1,158 were differentially expressed in the leaf sheaths (548 up-regulated and 610 down-regulated) and 492 in the roots (276 up, 216 down). Among the 36 deficiency-induced genes first identified via RNA-Seq analyses, 34 were subsequently confirmed by qRT-PCR. Our RNA-Seq data identified 8,509 multi-exonic genes with 19,628 alternative splicing events. However, we saw no significant difference in alternative splicing between N-sufficient and -deficient conditions. We found 2,986 novel transcripts, of which 192 were regulated under the N-deficiency. Conclusion We identified 1,650 genes that were differentially expressed after 12?h of N-starvation. Responses by those genes to a limited supply of N were confirmed by RT-PCR and GUS assays. Our results provide valuable information about N-starvation-responsive genes and will be useful when investigating the signal transduction pathway of N-utilization.
机译:背景技术氮(N)是植物生长和发育的关键常量营养素,它是大多数农业系统中的主要限制因素。已经进行了微阵列分析以调查全基因组基因表达对N浓度变化的响应。尽管RNA-Seq分析可以提供更精确的转录水平测定,但以前尚未用于研究N-饥饿诱导基因的表达。结果我们从在缺氮或充足条件下生长12?h的水稻植株的叶鞘和根部构建cDNA文库。对文库进行测序导致鉴定了33,782个带注释的基因。丰度的比较显示,由于N缺乏,差异表达(折叠倍数≥2)的1,650个转录本。其中,在叶鞘中有1158个差异表达(548个上调和610个下调),在根中有492个(276个上调,216个下调)。首先通过RNA-Seq分析鉴定出的36种缺陷诱导基因中,随后通过qRT-PCR证实了34种。我们的RNA-Seq数据确定了8,509个外显子基因,其中包含19,628个可变剪接事件。但是,我们发现在N充分条件和-充分条件之间的替代剪接中没有显着差异。我们发现了2,986篇新颖的成绩单,其中有192篇受到N缺陷调控。结论我们鉴定了1,650个在N饥饿12h后差异表达的基因。 RT-PCR和GUS分析证实了这些基因对有限氮供应的反应。我们的结果提供了有关N饥饿反应基因的有价值的信息,并且在研究N利用的信号转导途径时将很有用。

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