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白皮松转录组中 microRNA 的鉴定与特征分析。

Transcriptome-wide identification and characterization of miRNAs from Pinus densata.

机构信息

Key Laboratory of Plant Molecular Physiology, Institute of Botany, Chinese Academy of Sciences, Beijing 100093, China.

出版信息

BMC Genomics. 2012 Apr 6;13:132. doi: 10.1186/1471-2164-13-132.

Abstract

BACKGROUND

MicroRNAs (miRNAs) play key roles in diverse developmental processes, nutrient homeostasis and responses to biotic and abiotic stresses. The biogenesis and regulatory functions of miRNAs have been intensively studied in model angiosperms, such as Arabidopsis thaliana, Oryza sativa and Populus trichocarpa. However, global identification of Pinus densata miRNAs has not been reported in previous research.

RESULTS

Here, we report the identification of 34 conserved miRNAs belonging to 25 miRNA families from a P. densata mRNA transcriptome database using local BLAST and MIREAP programs. The primary and/or precursor sequences of 29 miRNAs were further confirmed by RT-PCR amplification and subsequent sequencing. The average value of the minimal folding free energy indexes of the 34 miRNA precursors was 0.92. Nineteen (58%) mature miRNAs began with a 5' terminal uridine residue. Analysis of miRNA precursors showed that 19 mature miRNAs were novel members of 14 conserved miRNA families, of which 17 miRNAs were further validated by subcloning and sequencing. Using real-time quantitative RT-PCR, we found that the expression levels of 7 miRNAs were more than 2-fold higher in needles than in stems. In addition, 72 P. densata mRNAs were predicted to be targets of 25 miRNA families. Four target genes, including a nodal modulator 1-like protein gene, two GRAS family transcription factor protein genes and one histone deacetylase gene, were experimentally verified to be the targets of 3 P. densata miRNAs, pde-miR162a, pde-miR171a and pde-miR482a, respectively.

CONCLUSIONS

This study led to the discovery of 34 conserved miRNAs comprising 25 miRNA families from Pinus densata. These results lay a solid foundation for further studying the regulative roles of miRNAs in the development, growth and responses to environmental stresses in P. densata.

摘要

背景

微小 RNA(miRNA)在多种发育过程、养分稳态以及生物和非生物胁迫反应中发挥关键作用。miRNA 的生物发生和调控功能已在拟南芥、水稻和毛白杨等模式被子植物中得到深入研究。然而,在之前的研究中,尚未报道过云南松 miRNA 的全局鉴定。

结果

在这里,我们使用本地 BLAST 和 MIREAP 程序,从云南松 mRNA 转录组数据库中报告了 34 个属于 25 个 miRNA 家族的保守 miRNA 的鉴定。29 个 miRNA 的初级和/或前体序列通过 RT-PCR 扩增和随后的测序进一步证实。34 个 miRNA 前体的最小折叠自由能指数的平均值为 0.92。19 个(58%)成熟 miRNA 以 5'端尿嘧啶残基开始。miRNA 前体分析表明,19 个成熟 miRNA 是 14 个保守 miRNA 家族的新成员,其中 17 个 miRNA 通过亚克隆和测序进一步验证。使用实时定量 RT-PCR,我们发现 7 个 miRNA 在针中的表达水平比在茎中高 2 倍以上。此外,预测到 72 个云南松 mRNAs 是 25 个 miRNA 家族的靶标。四个靶基因,包括一个节点调节剂 1 样蛋白基因、两个 GRAS 家族转录因子蛋白基因和一个组蛋白去乙酰化酶基因,被实验验证为 3 个云南松 miRNA,pde-miR162a、pde-miR171a 和 pde-miR482a 的靶标。

结论

本研究从云南松中发现了 34 个保守 miRNA,包含 25 个 miRNA 家族。这些结果为进一步研究 miRNA 在云南松发育、生长和对环境胁迫反应中的调控作用奠定了基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ce21/3347991/5e6c8bdd7236/1471-2164-13-132-1.jpg

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