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Journal of Zhejiang University SCIENCE B
ISSN 1673-1581(Print), 1862-1783(Online), Monthly
2014 Vol.15 No.2 P.125-132
Analysis of promoters of microRNAs from a Glycine max degradome library
Abstract: Objective: MicroRNAs (miRNAs) are genome-encoded, small non-coding RNAs that play important functions in development, biotic and abiotic stress responses, and other processes. Our aim was to explore the regulation of miRNA expression. Methods: We used bioinformatics methods to predict the core promoters of 440 miRNAs identified from a soybean (Glycine max) degradome library and to analyze cis-acting elements for 369 miRNAs. Results: The prediction results showed that 83.86% of the 440 miRNAs contained promoters in their upstream sequences, and 8.64% (38 loci) in their downstream sequences. The distributions of two core promoter elements, TATA-boxes and transcription start sites (TSSs), were similar. The cis-acting elements were examined to provide clues to the function and regulation of spatiotemporal expression of the miRNAs. Analyses of miRNA cis-elements and targets indicated a potential auxin response factor (ARF)- and gibberellin response factor (GARF)-mediated negative feedback loop for miRNA expression. Conclusions: The features of miRNAs from a Glycine max degradome library obtained here provide insights into the transcription regulation and functions of miRNAs in soybean.
Key words: Glycine max, MicroRNA (miRNA), Promoter, Cis-acting element, Prediction
The online version of this article contains supplementary materials Table S1, Table S2, and Table S3
创新要点:利用生物信息学方法全面解析了大豆降解组文库miRNA的启动子特征,并依据顺式作用元件及靶基因构建了miRNA的表达与生长素响应因子、赤霉素响应因子之间存在潜在的负反馈调控网络。
研究方法:本研究利用TSSP 程序和PlantCARE数据库预测了来自大豆降解组文库的440个miRNA的核心启动子以及369个miRNAs的顺式作用元件,并依据顺式作用元件及靶基因构建miRNA调控网络。
重要结论:83.86%的miRNA在其上游序列中含有启动子,8.64%的miRNA在其下游序列中含有启动子,21.59%的miRNA包含增强子。核心启动子的TATA盒与转录起始位点(TSSs)的分布相似(见图2)。此外,对转录起始位点5'端的顺式作用元件预测为miRNAs的可能功能和表达的时空性提供了线索。miRNAs的顺式作用元件和靶基因的分析显示,部分miRNA的表达与生长素响应因子、赤霉素响应因子之间存在潜在的负反馈调控(见图3)。
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DOI:
10.1631/jzus.B1300179
CLC number:
Q522+.6
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On-line Access:
2024-08-27
Received:
2023-10-17
Revision Accepted:
2024-05-08
Crosschecked:
2014-01-14