滴虫中保守mirna及其靶点的计算鉴定、表征和分析

B. Hajieghrari, N. Farrokhi, B. Goliaei, K. Kavousi
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引用次数: 12

摘要

MicroRNAs (miRNAs)是一种单链非编码内源性小rna,大约有22个核苷酸,在转录后水平直接参与基因表达调控。mirna在生物和非生物胁迫的发育和响应中发挥关键作用。同源性搜索允许鉴定新的mirna,因为它们在植物物种中相对较高的保守性。在这里,鉴定出了滴虫Amborella trichopoda的mirna。从miRBase中提取已知的和独特的植物miRNAs,对毛蛾的表达序列标签(EST)和基因组调查序列(GSS)进行blast检索。通过一系列miRNA过滤标准筛选具有适当折叠结构的候选序列。最后,我们鉴定并分析了来自est的5个miRNA基因家族的5个潜在保守miRNA,以及来自gss的82个新鉴定的miRNA依赖的39个miRNA家族。利用psRNATarget对毛螺旋藻基因组序列的支架定位,根据miRNAs与相应miRNAs序列的序列互补性,鉴定鉴定出潜在的靶基因。总共鉴定出1219个毛虫基因组的目标位点。其中941个(77.19%)是miRNA切割的对象,278个(22.81%)是通过mRNA的翻译抑制来调节的。从预测的mirna中,有18个没有在毛螺旋藻中找到目标序列。
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Computational Identification, Characterization and Analysis of Conserved miRNAs and their Targets in Amborella Trichopoda
MicroRNAs (miRNAs) are single stranded non-coding endogenous small RNAs of about 22 nucleotides, which are directly involved in regulating gene expression at post transcriptional level. miRNAs play key roles in development and response to biotic and abiotic stresses. Homology searches allow identification of new miRNAs due to their relative high conservation in plant species. Here, miRNAs were identified for Amborella trichopoda. Known and unique plant miRNAs from miRBase were BLAST-searched against Expressed Sequence Tag (EST) and Genomic Survey Sequence (GSS) in A. trichopoda. All candidate sequences with appropriate fold back structure were screened by a series of miRNA filtering criteria. Finally, we identified and analysed conservation of 5 potential conserved miRNAs belonging to 5 miRNA gene families from ESTs as well 82 newly identified miRNAs dependant 39 miRNA families from GSSs. Potential target genes of identified miRNAs were identified based on their sequence complementarities to the respective miRNAs using psRNATarget against scaffold assignment of A. trichopoda genome sequences. Totally, 1219 target sites in A. trichopoda genome were identified. From which, 941 (77.19%) were predicted to be the subject of miRNA cleavage and 278 (22.81%) scaffolds were regulated via translational repression of mRNA. From the predicted miRNAs, 18 had no target sequence in A.trichopoda.
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