通过小 RNA 测序、基于微阵列杂交和基因组调查支架序列,在茶树(Camellia sinensis)的一个芽和两片嫩叶中进行全基因组保守和新型 microRNA 的鉴定。

Genome-wide identification of conserved and novel microRNAs in one bud and two tender leaves of tea plant (Camellia sinensis) by small RNA sequencing, microarray-based hybridization and genome survey scaffold sequences.

机构信息

State Key Laboratory of Tea Plant Biology and Utilization, Anhui Agricultural University, 130 Changjiang West Road, Hefei, Anhui Province, 230036, People's Republic of China.

Department of Biotechnology, Karpagam University, Coimbatore, India.

出版信息

BMC Plant Biol. 2017 Nov 21;17(1):212. doi: 10.1186/s12870-017-1169-1.

Abstract

BACKGROUND

MicroRNAs (miRNAs) are important for plant growth and responses to environmental stresses via post-transcriptional regulation of gene expression. Tea, which is primarily produced from one bud and two tender leaves of the tea plant (Camellia sinensis), is one of the most popular non-alcoholic beverages worldwide owing to its abundance of secondary metabolites. A large number of miRNAs have been identified in various plants, including non-model species. However, due to the lack of reference genome sequences and/or information of tea plant genome survey scaffold sequences, discovery of miRNAs has been limited in C. sinensis.

RESULTS

Using small RNA sequencing, combined with our recently obtained genome survey data, we have identified and analyzed 175 conserved and 83 novel miRNAs mainly in one bud and two tender leaves of the tea plant. Among these, 93 conserved and 18 novel miRNAs were validated using miRNA microarray hybridization. In addition, the expression pattern of 11 conserved and 8 novel miRNAs were validated by stem-loop-qRT-PCR. A total of 716 potential target genes of identified miRNAs were predicted. Further, Gene Ontology (GO) and the Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway analysis revealed that most of the target genes were primarily involved in stress response and enzymes related to phenylpropanoid biosynthesis. The predicted targets of 4 conserved miRNAs were further validated by 5'RLM-RACE. A negative correlation between expression profiles of 3 out of 4 conserved miRNAs (csn-miR160a-5p, csn-miR164a, csn-miR828 and csn-miR858a) and their targets (ARF17, NAC100, WER and MYB12 transcription factor) were observed.

CONCLUSION

In summary, the present study is one of few such studies on miRNA detection and identification in the tea plant. The predicted target genes of majority of miRNAs encoded enzymes, transcription factors, and functional proteins. The miRNA-target transcription factor gene interactions may provide important clues about the regulatory mechanism of these miRNAs in the tea plant. The data reported in this study will make a huge contribution to knowledge on the potential miRNA regulators of the secondary metabolism pathway and other important biological processes in C. sinensis.

摘要

背景

微小 RNA(miRNA)通过基因表达的转录后调控在植物生长和对环境胁迫的响应中发挥着重要作用。茶是一种主要由茶树的一个芽和两片嫩叶制成的饮品,由于其丰富的次生代谢产物,是全球最受欢迎的非酒精饮料之一。在包括非模式物种在内的各种植物中,已经鉴定出大量的 miRNA。然而,由于缺乏茶树参考基因组序列和/或基因组调查支架序列的信息,导致在茶树中 miRNA 的发现受到限制。

结果

我们使用小 RNA 测序技术,结合我们最近获得的基因组调查数据,在茶树的一个芽和两片嫩叶中鉴定和分析了 175 个保守和 83 个新的 miRNA。其中,93 个保守和 18 个新的 miRNA 通过 miRNA 微阵列杂交得到验证。此外,通过茎环-qRT-PCR 验证了 11 个保守和 8 个新的 miRNA 的表达模式。共预测了 716 个鉴定 miRNA 的潜在靶基因。进一步的基因本体(GO)和京都基因与基因组百科全书(KEGG)途径分析表明,大多数靶基因主要参与应激反应和与苯丙烷生物合成相关的酶。预测的 miRNA 靶基因进一步通过 5'RLM-RACE 进行验证。4 个保守 miRNA 的预测靶基因中有 3 个(csn-miR160a-5p、csn-miR164a、csn-miR828 和 csn-miR858a)及其靶基因(ARF17、NAC100、WER 和 MYB12 转录因子)之间的表达谱呈负相关。

结论

综上所述,本研究是茶树 miRNA 检测和鉴定的少数研究之一。大多数 miRNA 的预测靶基因编码酶、转录因子和功能蛋白。miRNA-靶转录因子基因相互作用可能为这些 miRNA 在茶树中的调控机制提供重要线索。本研究报告的数据将为茶树次生代谢途径和其他重要生物学过程的潜在 miRNA 调控因子的知识做出巨大贡献。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d97e/5697157/3fa498ec990c/12870_2017_1169_Fig1_HTML.jpg

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