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番茄(Lycopersicon esculentum)中保守微小RNA及其靶基因的鉴定。

Identification of conserved microRNAs and their target genes in tomato (Lycopersicon esculentum).

作者信息

Yin Zujun, Li Chunhe, Han Xiulan, Shen Fafu

机构信息

State Key Laboratory of Crop Biology, College of Agronomy, Shandong Agricultural University, Tai'an, Shandong, PR China.

出版信息

Gene. 2008 May 15;414(1-2):60-6. doi: 10.1016/j.gene.2008.02.007. Epub 2008 Feb 20.

Abstract

MicroRNAs (miRNAs) are a class of non-coding RNAs that have important gene regulation roles in various organisms. To date, a total of 1279 plant miRNAs have been deposited in the miRNA miRBase database (Release 10.1). Many of them are conserved during the evolution of land plants suggesting that the well-conserved miRNAs may also retain homologous target interactions. Recently, little is known about the experimental or computational identification of conserved miRNAs and their target genes in tomato. Here, using a computational homology search approach, 21 conserved miRNAs were detected in the Expressed Sequence Tags (EST) and Genomic Survey Sequence (GSS) databases. Following this, 57 potential target genes were predicted by searching the mRNA database. Most of the target mRNAs appeared to be involved in plant growth and development. Our findings verified that the well-conserved tomato miRNAs have retained homologous target interactions amongst divergent plant species. Some miRNAs express diverse combinations in different cell types and have been shown to regulate cell-specific target genes coordinately. We believe that the targeting propensity for genes in different biological processes can be explained largely by their protein connectivity.

摘要

微小RNA(miRNA)是一类非编码RNA,在各种生物体中具有重要的基因调控作用。截至目前,共有1279种植物miRNA已存入miRNA miRBase数据库(版本10.1)。其中许多在陆地植物进化过程中是保守的,这表明高度保守的miRNA可能也保留了同源靶标相互作用。最近,关于番茄中保守miRNA及其靶基因的实验或计算鉴定知之甚少。在此,利用计算同源性搜索方法,在表达序列标签(EST)和基因组调查序列(GSS)数据库中检测到21种保守miRNA。随后,通过搜索mRNA数据库预测了57个潜在靶基因。大多数靶mRNA似乎参与植物生长和发育。我们的研究结果证实,高度保守的番茄miRNA在不同植物物种间保留了同源靶标相互作用。一些miRNA在不同细胞类型中表达不同组合,并已显示可协调调控细胞特异性靶基因。我们认为,不同生物学过程中基因的靶向倾向在很大程度上可以通过它们的蛋白质连接性来解释。

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