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‘MicroRNA 靶点’,一个新的 AthaMap 网络工具,用于在拟南芥中进行全基因组 miRNA 靶点的鉴定。

'MicroRNA Targets', a new AthaMap web-tool for genome-wide identification of miRNA targets in Arabidopsis thaliana.

机构信息

Institut für Genetik, Technische Universität Braunschweig, Spielmannstr, 38106, Braunschweig, Germany.

出版信息

BioData Min. 2012 Jul 16;5(1):7. doi: 10.1186/1756-0381-5-7.

Abstract

BACKGROUND

The AthaMap database generates a genome-wide map for putative transcription factor binding sites for A. thaliana. When analyzing transcriptional regulation using AthaMap it may be important to learn which genes are also post-transcriptionally regulated by inhibitory RNAs. Therefore, a unified database for transcriptional and post-transcriptional regulation will be highly useful for the analysis of gene expression regulation.

METHODS

To identify putative microRNA target sites in the genome of A. thaliana, processed mature miRNAs from 243 annotated miRNA genes were used for screening with the psRNATarget web server. Positional information, target genes and the psRNATarget score for each target site were annotated to the AthaMap database. Furthermore, putative target sites for small RNAs from seven small RNA transcriptome datasets were used to determine small RNA target sites within the A. thaliana genome.

RESULTS

Putative 41,965 genome wide miRNA target sites and 10,442 miRNA target genes were identified in the A. thaliana genome. Taken together with genes targeted by small RNAs from small RNA transcriptome datasets, a total of 16,600 A. thaliana genes are putatively regulated by inhibitory RNAs. A novel web-tool, 'MicroRNA Targets', was integrated into AthaMap which permits the identification of genes predicted to be regulated by selected miRNAs. The predicted target genes are displayed with positional information and the psRNATarget score of the target site. Furthermore, putative target sites of small RNAs from selected tissue datasets can be identified with the new 'Small RNA Targets' web-tool.

CONCLUSIONS

The integration of predicted miRNA and small RNA target sites with transcription factor binding sites will be useful for AthaMap-assisted gene expression analysis. URL: http://www.athamap.de/

摘要

背景

AthaMap 数据库为拟南芥的潜在转录因子结合位点生成全基因组图谱。在使用 AthaMap 分析转录调控时,了解哪些基因也受到抑制性 RNA 的转录后调控可能很重要。因此,一个用于转录和转录后调控的统一数据库将非常有助于分析基因表达调控。

方法

为了鉴定拟南芥基因组中潜在的 microRNA 靶位点,使用 243 个注释的 miRNA 基因的成熟 miRNA 进行筛选,使用 psRNATarget 网络服务器进行筛选。将每个靶位点的位置信息、靶基因和 psRNATarget 得分注释到 AthaMap 数据库中。此外,还使用来自七个小 RNA 转录组数据集的小 RNA 前体来确定拟南芥基因组内的小 RNA 靶位点。

结果

在拟南芥基因组中鉴定出 41965 个全基因组 miRNA 靶位点和 10442 个 miRNA 靶基因。加上来自小 RNA 转录组数据集的小 RNA 靶向的基因,共有 16600 个拟南芥基因被抑制性 RNA 靶向调控。一个新的网络工具“MicroRNA Targets”被集成到 AthaMap 中,允许鉴定出被选定 miRNA 预测调控的基因。预测的靶基因显示位置信息和靶位点的 psRNATarget 得分。此外,还可以使用新的“Small RNA Targets”网络工具识别来自选定组织数据集的小 RNA 的潜在靶位点。

结论

将预测的 miRNA 和小 RNA 靶位点与转录因子结合位点整合在一起,将有助于 AthaMap 辅助的基因表达分析。网址:http://www.athamap.de/

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