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高通量深度降解组测序揭示了桑树(Morus alba)响应干旱胁迫时的微小RNA及其靶标。

High throughput deep degradome sequencing reveals microRNAs and their targets in response to drought stress in mulberry (Morus alba).

作者信息

Li Ruixue, Chen Dandan, Wang Taichu, Wan Yizhen, Li Rongfang, Fang Rongjun, Wang Yuting, Hu Fei, Zhou Hong, Li Long, Zhao Weiguo

机构信息

School of Biology and Technology, Jiangsu University of Science and Technology, Zhenjiang, Jiangsu, P. R. China.

The Sericultural Research Institute, Anhui Academy of Agricultural Sciences, Hefei, Anhui, P. R. China.

出版信息

PLoS One. 2017 Feb 24;12(2):e0172883. doi: 10.1371/journal.pone.0172883. eCollection 2017.

Abstract

MicroRNAs (miRNAs) play important regulatory roles by targeting mRNAs for cleavage or translational repression. Identification of miRNA targets is essential to better understanding the roles of miRNAs. miRNA targets have not been well characterized in mulberry (Morus alba). To anatomize miRNA guided gene regulation under drought stress, transcriptome-wide high throughput degradome sequencing was used in this study to directly detect drought stress responsive miRNA targets in mulberry. A drought library (DL) and a contrast library (CL) were constructed to capture the cleaved mRNAs for sequencing. In CL, 409 target genes of 30 conserved miRNA families and 990 target genes of 199 novel miRNAs were identified. In DL, 373 target genes of 30 conserved miRNA families and 950 target genes of 195 novel miRNAs were identified. Of the conserved miRNA families in DL, mno-miR156, mno-miR172, and mno-miR396 had the highest number of targets with 54, 52 and 41 transcripts, respectively, indicating that these three miRNA families and their target genes might play important functions in response to drought stress in mulberry. Additionally, we found that many of the target genes were transcription factors. By analyzing the miRNA-target molecular network, we found that the DL independent networks consisted of 838 miRNA-mRNA pairs (63.34%). The expression patterns of 11 target genes and 12 correspondent miRNAs were detected using qRT-PCR. Six miRNA targets were further verified by RNA ligase-mediated 5' rapid amplification of cDNA ends (RLM-5' RACE). Gene Ontology (GO) annotations and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway analysis revealed that these target transcripts were implicated in a broad range of biological processes and various metabolic pathways. This is the first study to comprehensively characterize target genes and their associated miRNAs in response to drought stress by degradome sequencing in mulberry. This study provides a framework for understanding the molecular mechanisms of drought resistance in mulberry.

摘要

微小RNA(miRNA)通过靶向mRNA进行切割或翻译抑制发挥重要的调控作用。鉴定miRNA靶标对于更好地理解miRNA的作用至关重要。桑树(Morus alba)中miRNA靶标尚未得到很好的表征。为了解析干旱胁迫下miRNA介导的基因调控,本研究采用全转录组高通量降解组测序直接检测桑树中干旱胁迫响应的miRNA靶标。构建了一个干旱文库(DL)和一个对照文库(CL)以捕获切割后的mRNA进行测序。在CL中,鉴定出30个保守miRNA家族的409个靶基因和199个新miRNA的990个靶基因。在DL中,鉴定出30个保守miRNA家族的373个靶基因和195个新miRNA的950个靶基因。在DL中的保守miRNA家族中,mno-miR156、mno-miR172和mno-miR396的靶标数量最多,分别有54、52和41个转录本,表明这三个miRNA家族及其靶基因可能在桑树对干旱胁迫的响应中发挥重要作用。此外,我们发现许多靶基因是转录因子。通过分析miRNA-靶标分子网络,我们发现DL独立网络由838个miRNA- mRNA对组成(63.34%)。使用qRT-PCR检测了11个靶基因和12个相应miRNA的表达模式。通过RNA连接酶介导的5' cDNA末端快速扩增(RLM-5' RACE)进一步验证了6个miRNA靶标。基因本体论(GO)注释和京都基因与基因组百科全书(KEGG)通路分析表明,这些靶转录本涉及广泛的生物学过程和各种代谢途径。这是第一项通过桑树降解组测序全面表征响应干旱胁迫的靶基因及其相关miRNA的研究。本研究为理解桑树抗旱的分子机制提供了一个框架。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/532b/5325578/580ae067abfd/pone.0172883.g001.jpg

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