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利用全基因组高通量测序鉴定和综合分析水稻中草甘膦胁迫响应的 microRNAs、lncRNAs 和 mRNAs。

Identification and integrated analysis of glyphosate stress-responsive microRNAs, lncRNAs, and mRNAs in rice using genome-wide high-throughput sequencing.

机构信息

Institute of Crop and Nuclear Technology Utilization, Zhejiang Academy of Agricultural Sciences, 198, Shiqiao Road, Hangzhou, 310021, Zhejiang, China.

RiceTec Inc, Alvin, TX, 77511, USA.

出版信息

BMC Genomics. 2020 Mar 17;21(1):238. doi: 10.1186/s12864-020-6637-6.

Abstract

BACKGROUND

Glyphosate has become the most widely used herbicide in the world. Therefore, the development of new varieties of glyphosate-tolerant crops is a research focus of seed companies and researchers. The glyphosate stress-responsive genes were used for the development of genetically modified crops, while only the EPSPS gene has been used currently in the study on glyphosate-tolerance in rice. Therefore, it is essential and crucial to intensify the exploration of glyphosate stress-responsive genes, to not only acquire other glyphosate stress-responsive genes with clean intellectual property rights but also obtain non-transgenic glyphosate-tolerant rice varieties. This study is expected to elucidate the responses of miRNAs, lncRNAs, and mRNAs to glyphosate applications and the potential regulatory mechanisms in response to glyphosate stress in rice.

RESULTS

Leaves of the non-transgenic glyphosate-tolerant germplasm CA21 sprayed with 2 mg·ml glyphosate (GLY) and CA21 plants with no spray (CK) were collected for high-throughput sequencing analysis. A total of 1197 DEGs, 131 DELs, and 52 DEMs were identified in the GLY samples in relation to CK samples. Genes were significantly enriched for various biological processes involved in detoxification of plant response to stress. A total of 385 known miRNAs from 59 miRNA families and 94 novel miRNAs were identified. Degradome analysis led to the identification of 32 target genes, of which, the squamosa promoter-binding-like protein 12 (SPL12) was identified as a target of osa-miR156a_L + 1. The lncRNA-miRNA-mRNA regulatory network consisted of osa-miR156a_L + 1, two transcripts of SPL12 (LOC_Os06g49010.3 and LOC_Os06g49010.5), and 13 lncRNAs (e.g., MSTRG.244.1 and MSTRG.16577.1).

CONCLUSION

Large-scale expression changes in coding and noncoding RNA were observed in rice mainly due to its response to glyphosate. SPL12, osa-miR156, and lncRNAs (e.g., MSTRG.244.1 and MSTRG.16577.1) could be a novel ceRNA mechanism in response to glyphosate in rice by regulating transcription and metal ions binding. These findings provide a theoretical basis for breeding glyphosate-tolerant rice varieties and for further research on the biogenesis of glyphosate- tolerance in rice.

摘要

背景

草甘膦已成为世界上使用最广泛的除草剂。因此,开发新的草甘膦耐受作物品种是种子公司和研究人员的研究重点。草甘膦胁迫响应基因被用于开发转基因作物,而目前在研究水稻草甘膦耐受性方面仅使用 EPSPS 基因。因此,加强对草甘膦胁迫响应基因的探索至关重要,不仅要获得其他具有清洁知识产权的草甘膦胁迫响应基因,还要获得非转基因的草甘膦耐受水稻品种。本研究有望阐明 miRNA、lncRNA 和 mRNA 对草甘膦应用的响应以及水稻对草甘膦胁迫响应的潜在调控机制。

结果

用 2mg·ml 草甘膦(GLY)喷洒的非转基因草甘膦耐受种质 CA21 和未喷洒的 CA21 植株(CK)叶片进行高通量测序分析。在 GLY 样品中与 CK 样品相比,共鉴定出 1197 个差异表达基因(DEGs)、131 个差异外显子(DELs)和 52 个差异剪接体(DEMs)。基因显著富集于各种生物过程,包括植物对胁迫的解毒反应。共鉴定出 59 个 miRNA 家族的 385 个已知 miRNA 和 94 个新的 miRNA。降解组分析导致鉴定出 32 个靶基因,其中,伞状结构域结合蛋白 12(SPL12)被鉴定为 osa-miR156a_L+1 的靶标。lncRNA-miRNA-mRNA 调控网络由 osa-miR156a_L+1、SPL12 的两个转录本(LOC_Os06g49010.3 和 LOC_Os06g49010.5)和 13 个 lncRNA(如 MSTRG.244.1 和 MSTRG.16577.1)组成。

结论

水稻主要由于对草甘膦的反应,导致编码和非编码 RNA 的大规模表达变化。SPL12、osa-miR156 和 lncRNAs(如 MSTRG.244.1 和 MSTRG.16577.1)可能通过调节转录和金属离子结合,成为水稻响应草甘膦的新型 ceRNA 机制。这些发现为培育草甘膦耐受水稻品种和进一步研究水稻草甘膦耐受的生物发生提供了理论基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4abf/7076996/fa8ef90a5ce7/12864_2020_6637_Fig1_HTML.jpg

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