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本文引用的文献

1
Expression-based functional investigation of the organ-specific microRNAs in Arabidopsis.基于表达谱的拟南芥组织特异性 microRNA 功能研究。
PLoS One. 2012;7(11):e50870. doi: 10.1371/journal.pone.0050870. Epub 2012 Nov 30.
2
Methods for validation of miRNA sequence variants and the cleavage of their targets.miRNA 序列变异体的验证方法及其靶标的切割。
Methods. 2012 Oct;58(2):135-43. doi: 10.1016/j.ymeth.2012.08.005. Epub 2012 Aug 17.
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IsomiRs--the overlooked repertoire in the dynamic microRNAome.IsomiRs——动态 microRNAome 中被忽视的文库。
Trends Genet. 2012 Nov;28(11):544-9. doi: 10.1016/j.tig.2012.07.005. Epub 2012 Aug 8.
4
Reconstitution of an Argonaute-dependent small RNA biogenesis pathway reveals a handover mechanism involving the RNA exosome and the exonuclease QIP.重建依赖 Argonaute 的小 RNA 生物发生途径揭示了一种涉及 RNA 外切酶复合物和核酸外切酶 QIP 的交接机制。
Mol Cell. 2012 May 11;46(3):299-310. doi: 10.1016/j.molcel.2012.03.019. Epub 2012 Apr 17.
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MicroRNA profiling: approaches and considerations.miRNA 分析:方法与考虑因素。
Nat Rev Genet. 2012 Apr 18;13(5):358-69. doi: 10.1038/nrg3198.
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Plant secondary siRNA production determined by microRNA-duplex structure.植物二级 siRNA 的产生由 microRNA 二聚体结构决定。
Proc Natl Acad Sci U S A. 2012 Feb 14;109(7):2461-6. doi: 10.1073/pnas.1200169109. Epub 2012 Jan 30.
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Massive analysis of rice small RNAs: mechanistic implications of regulated microRNAs and variants for differential target RNA cleavage.大规模水稻小 RNA 分析:调控 microRNAs 和变体对差异靶 RNA 切割的机制影响。
Plant Cell. 2011 Dec;23(12):4185-207. doi: 10.1105/tpc.111.089045. Epub 2011 Dec 9.
8
MicroRNAs as master regulators of the plant NB-LRR defense gene family via the production of phased, trans-acting siRNAs.MicroRNAs 通过产生有相位的、反式作用的 siRNAs 作为植物 NB-LRR 防御基因家族的主调控因子。
Genes Dev. 2011 Dec 1;25(23):2540-53. doi: 10.1101/gad.177527.111.
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High-resolution experimental and computational profiling of tissue-specific known and novel miRNAs in Arabidopsis.在拟南芥中进行组织特异性已知和新型 miRNA 的高分辨率实验和计算分析。
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Post-transcriptional generation of miRNA variants by multiple nucleotidyl transferases contributes to miRNA transcriptome complexity.多种核苷酸转移酶在后转录水平产生 miRNA 变体,有助于 miRNA 转录组的复杂性。
Genome Res. 2011 Sep;21(9):1450-61. doi: 10.1101/gr.118059.110. Epub 2011 Aug 3.

通过分析序列变异、表达模式、ARGONAUTE 加载和靶标切割来增强 microRNA 的综合研究。

Comprehensive investigation of microRNAs enhanced by analysis of sequence variants, expression patterns, ARGONAUTE loading, and target cleavage.

机构信息

Delaware Biotechnology Institute, University of Delaware, Newark, Delaware 19711, USA.

出版信息

Plant Physiol. 2013 Jul;162(3):1225-45. doi: 10.1104/pp.113.219873. Epub 2013 May 24.

DOI:10.1104/pp.113.219873
PMID:23709668
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3707554/
Abstract

MicroRNAs (miRNAs) are a class of small RNAs that typically function by guiding the cleavage of target messenger RNAs. They have been shown to play major roles in a variety of plant processes, including development, and responses to pathogens and environmental stresses. To identify new miRNAs and regulation in Arabidopsis (Arabidopsis thaliana), 27 small RNA libraries were constructed and sequenced from various tissues, stresses, and small RNA biogenesis mutants, resulting in 95 million genome-matched sequences. The use of rdr2 to enrich the miRNA population greatly enhanced this analysis and led to the discovery of new miRNAs arising from both known and new precursors, increasing the total number of Arabidopsis miRNAs by about 10%. Parallel Analysis of RNA Ends data provide evidence that the majority guide target cleavage. Many libraries represented novel stress/tissue conditions, such as submergence-stressed flowers, which enabled the identification of new stress regulation of both miRNAs and their targets, all of which were validated in wild-type plants. By combining small RNA expression analysis with ARGONAUTE immunoprecipitation data and global target cleavage data from Parallel Analysis of RNA Ends, a much more complete picture of Arabidopsis miRNAs was obtained. In particular, the discovery of ARGONAUTE loading and target cleavage biases gave important insights into tissue-specific expression patterns, pathogen responses, and the role of sequence variation among closely related miRNA family members that would not be evident without this combinatorial approach.

摘要

微小 RNA(miRNAs)是一类小 RNA,通常通过引导靶信使 RNA 的切割发挥作用。它们已被证明在多种植物过程中发挥重要作用,包括发育以及对病原体和环境胁迫的反应。为了鉴定拟南芥(Arabidopsis thaliana)中的新 miRNAs 和调控,从各种组织、胁迫和 miRNA 生物发生突变体构建并测序了 27 个小 RNA 文库,产生了 9500 万个与基因组匹配的序列。使用 rdr2 富集 miRNA 群体极大地增强了这种分析,并发现了来自已知和新前体的新 miRNAs,使拟南芥 miRNAs 的总数增加了约 10%。RNA 末端平行分析数据提供了证据表明大多数 miRNA 指导靶标切割。许多文库代表了新的胁迫/组织条件,如淹没胁迫的花朵,这使得能够鉴定新的胁迫调节 miRNA 和它们的靶标,所有这些都在野生型植物中得到了验证。通过将小 RNA 表达分析与 ARGONAUTE 免疫沉淀数据和 RNA 末端平行分析的全球靶标切割数据相结合,获得了更完整的拟南芥 miRNAs 图谱。特别是,ARGONAUTE 加载和靶标切割偏向的发现为组织特异性表达模式、病原体反应以及密切相关 miRNA 家族成员之间序列变异的作用提供了重要的见解,如果没有这种组合方法,这些见解是不会明显的。