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Yin Z  Li C  Han X  Shen F 《Gene》2008,414(1-2):60-66
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.  相似文献   

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MicroRNA (miRNA) 是一类调控基因转录后表达的非编码的小分子RNA.它在生物的发育、细胞增殖、凋亡以及胁迫响应等生物过程中发挥着重要的调控作用.目前,分离和鉴定miRNA的方法主要包括实验方法(遗传筛选、直接克隆)和生物信息学方法.MiRNA存在表达丰度低,表达组织特异性,以及受特殊诱导等问题,用传统的实验法常难发现和鉴定miRNA.通过生物信息学方法在已有的各种基因库中寻找未知miRNA,大大提高了人们发现miRNA及其靶基因的效率.芸苔属(Brassica)的成员包括油菜、芜青、甘蓝等,是世界各国主要油料和食用作物.目前,油菜的miRNA的分离和鉴定工作已有文献报道,而其它的尚属空白.本文将拟南芥、水稻等植物已知的miRNA分别与芜青、甘蓝、野芥菜、黑芥菜、埃塞俄比亚芥的GSS和EST数据库进行比对搜索,采用一系列标准进行筛选,最后分别在芜青和甘蓝中预测到67个和95个miRNA.再把这些预测得到的miRNA分别与芜青和甘蓝的mRNA数据库进行比对搜索,分别找到120个和111个靶基因,除去未知功能及功能不详的,各有62个和48个靶基因.分析结果表明,上述大多数靶基因编码的产物为转录因子及重要代谢酶类,涉及植物的生长发育调控,信号转导及胁迫响应等方面.  相似文献   

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MicroRNAs (miRNAs) are small non-coding RNA molecules that play a vital role in the regulation of gene expression. Despite their identification in hundreds of plant species, few miRNAs have been identified in the Asteraceae, a large family that comprises approximately one tenth of all flowering plants. In this study, we used the expressed sequence tag (EST) analysis to identify potential conserved miRNAs and their putative target genes in the Asteraceae. We applied quantitative Real-Time PCR (qRT-PCR) to confirm the expression of eight potential miRNAs in Carthamus tinctorius and Helianthus annuus. We also performed qRT-PCR analysis to investigate the differential expression pattern of five newly identified miRNAs during five different cotyledon growth stages in safflower. Using these methods, we successfully identified and characterized 151 potentially conserved miRNAs, belonging to 26 miRNA families, in 11 genus of Asteraceae. EST analysis predicted that the newly identified conserved Asteraceae miRNAs target 130 total protein-coding ESTs in sunflower and safflower, as well as 433 additional target genes in other plant species. We experimentally confirmed the existence of seven predicted miRNAs, (miR156, miR159, miR160, miR162, miR166, miR396, and miR398) in safflower and sunflower seedlings. We also observed that five out of eight miRNAs are differentially expressed during cotyledon development. Our results indicate that miRNAs may be involved in the regulation of gene expression during seed germination and the formation of the cotyledons in the Asteraceae. The findings of this study might ultimately help in the understanding of miRNA-mediated gene regulation in important crop species.  相似文献   

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