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利用多种组学技术研究氮饥饿下水稻(Oryza sativa)基因和非编码 RNA 的转录组分析。

Transcriptomic analyses of rice (Oryza sativa) genes and non-coding RNAs under nitrogen starvation using multiple omics technologies.

机构信息

Department of Agricultural Biotechnology, Seoul National University, Seoul, 08826, Republic of Korea.

Interdisciplinary Program in Agricultural Genomics, Seoul National University, Seoul, 08826, Republic of Korea.

出版信息

BMC Genomics. 2018 Jul 13;19(1):532. doi: 10.1186/s12864-018-4897-1.

Abstract

BACKGROUND

Nitrogen (N) is a key macronutrient essential for plant growth, and its availability has a strong influence on crop development. The application of synthetic N fertilizers on crops has increased substantially in recent decades; however, the applied N is not fully utilized due to the low N use efficiency of crops. To overcome this limitation, it is important to understand the genome-wide responses and functions of key genes and potential regulatory factors in N metabolism.

RESULTS

Here, we characterized changes in the rice (Oryza sativa) transcriptome, including genes, newly identified putative long non-coding RNAs (lncRNAs), and microRNAs (miRNAs) and their target mRNAs in response to N starvation using four different transcriptome approaches. Analysis of rice genes involved in N metabolism and/or transport using strand-specific RNA-Seq identified 2588 novel putative lncRNA encoding loci. Analysis of previously published RNA-Seq datasets revealed a group of N starvation-responsive lncRNAs showing differential expression under other abiotic stress conditions. Poly A-primed sequencing (2P-Seq) revealed alternatively polyadenylated isoforms of N starvation-responsive lncRNAs and provided precise 3' end information on the transcript models of these lncRNAs. Analysis of small RNA-Seq data identified N starvation-responsive miRNAs and down-regulation of miR169 family members, causing de-repression of NF-YA, as confirmed by strand-specific RNA-Seq and qRT-PCR. Moreover, we profiled the N starvation-responsive down-regulation of root-specific miRNA, osa-miR444a.4-3p, and Degradome sequencing confirmed MADS25 as a novel target gene.

CONCLUSIONS

In this study, we used a combination of multiple RNA-Seq analyses to extensively profile the expression of genes, newly identified lncRNAs, and microRNAs in N-starved rice roots and shoots. Data generated in this study provide an in-depth understanding of the regulatory pathways modulated by N starvation-responsive miRNAs. The results of comprehensive, large-scale data analysis provide valuable information on multiple aspects of the rice transcriptome, which may be useful in understanding the responses of rice plants to changes in the N supply status of soil.

摘要

背景

氮(N)是植物生长所必需的关键大量营养素,其可利用性对作物发育有很强的影响。近几十年来,农作物对合成氮肥的应用大大增加;然而,由于作物对氮的利用效率低,施入的氮并未被完全利用。为了克服这一限制,了解氮代谢中关键基因和潜在调控因子的全基因组反应和功能非常重要。

结果

在这里,我们使用四种不同的转录组方法,描述了水稻(Oryza sativa)转录组中包括基因、新鉴定的假定长非编码 RNA(lncRNA)和 microRNA(miRNA)及其靶 mRNAs 对氮饥饿的响应变化。使用 RNA-Seq 对参与氮代谢和/或运输的水稻基因进行分析,鉴定出 2588 个新的假定 lncRNA 编码基因。对先前发表的 RNA-Seq 数据集的分析显示,一组氮饥饿响应的 lncRNA 在其他非生物胁迫条件下表现出差异表达。多聚 A 引物测序(2P-Seq)揭示了氮饥饿响应 lncRNA 的可变多聚腺苷酸化异构体,并提供了这些 lncRNA 转录模型的精确 3'端信息。对小 RNA-Seq 数据的分析鉴定了氮饥饿响应的 miRNA,并导致 NF-YA 的去抑制,这一点通过 RNA-Seq 和 qRT-PCR 得到了证实。此外,我们还分析了根特异性 miRNA osa-miR444a.4-3p 的氮饥饿响应下调,并通过降解组测序证实了 MADS25 是一个新的靶基因。

结论

在这项研究中,我们使用多种 RNA-Seq 分析的组合,广泛分析了氮饥饿水稻根和地上部中基因、新鉴定的 lncRNA 和 microRNA 的表达。本研究产生的数据深入了解了氮饥饿响应 miRNA 调节的调控途径。全面、大规模数据分析的结果提供了有关水稻转录组多个方面的有价值信息,这可能有助于理解水稻植物对土壤中氮供应状态变化的响应。

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