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Identification of new small non-coding RNAs from tobacco and Arabidopsis

机译:从烟草和拟南芥中鉴定新的小非编码小RNA

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Small non-coding RNAs (ncRNAs) have typically been searched in fully sequenced genomes using one of two approaches—experimental or computational. We developed a mixed method, using both types of information, which has the advantage of applying bio-computing methods to actually expressed sequences. Our method allowed the identification of new small ncRNAs in Arabidopsis thaliana and in the unfinished genome of Nicotiana tabacum. We constructed a N. tabacum cDNA library from small RNAs ranging from 20 to 30 nucleotides (nt). The sequences from 73 unique clones were compared to the A. thaliana genome and to all plant sequences using a pattern-matching approach (program Patbank). Thus, we selected 15 clones from the library corresponding mostly to A. thaliana or N. tabacum non-coding sequences. By Northern blot analyses, we confirmed the presence of most RNA candidates in Arabidopsis and in Nicotiana sylvestris with a size range of 21-100 nt. To gain more insight into the possible genesis of 21-24 nt sequences, stable folding of sRNAs with their flanking regions were predicted with the software MIRFOLD dedicated to the folding of microRNAs (miRNA). Stable hairpins structures were observed for some putative miRNAs.
机译:小型非编码RNA(ncRNA)通常使用实验或计算两种方法中的一种在完全测序的基因组中进行搜索。我们使用两种类型的信息开发了一种混合方法,该方法具有将生物计算方法应用于实际表达的序列的优势。我们的方法允许在拟南芥和未完成烟草基因组中鉴定新的小ncRNA。我们从20至30个核苷酸(nt)的小RNA构建了烟草烟草cDNA文库。使用模式匹配方法(程序Patbank)将来自73个独特克隆的序列与拟南芥基因组和所有植物序列进行比较。因此,我们从文库中选择了15个克隆,这些克隆主要对应于拟南芥或烟草的非编码序列。通过Northern印迹分析,我们确认了拟南芥和烟草中存在大多数RNA候选物,大小范围为21-100 nt。为了更深入地了解21-24 nt序列的可能成因,使用专用于microRNA(miRNA)折叠的软件MIRFOLD预测了sRNA及其侧翼区域的稳定折叠。对于某些推定的miRNA,观察到稳定的发夹结构。

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