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挖掘小RNA测序数据:一种鉴定拟南芥中小核仁RNA的新方法。

Mining small RNA sequencing data: a new approach to identify small nucleolar RNAs in Arabidopsis.

作者信息

Chen Ho-Ming, Wu Shu-Hsing

机构信息

Institute of Plant and Microbial Biology, Academia Sinica, Taiwan International Graduate Program, National Chung-Hsing University and Academia Sinica, Taipei, Taiwan.

出版信息

Nucleic Acids Res. 2009 May;37(9):e69. doi: 10.1093/nar/gkp225. Epub 2009 Apr 8.

Abstract

Small nucleolar RNAs (snoRNAs) are noncoding RNAs that direct 2'-O-methylation or pseudouridylation on ribosomal RNAs or spliceosomal small nuclear RNAs. These modifications are needed to modulate the activity of ribosomes and spliceosomes. A comprehensive repertoire of snoRNAs is needed to expand the knowledge of these modifications. The sequences corresponding to snoRNAs in 18-26-nt small RNA sequencing data have been rarely explored and remain as a hidden treasure for snoRNA annotation. Here, we showed the enrichment of small RNAs at Arabidopsis snoRNA termini and developed a computational approach to identify snoRNAs on the basis of this characteristic. The approach successfully uncovered the full-length sequences of 144 known Arabidopsis snoRNA genes, including some snoRNAs with improved 5'- or 3'-end annotation. In addition, we identified 27 and 17 candidates for novel box C/D and box H/ACA snoRNAs, respectively. Northern blot analysis and sequencing data from parallel analysis of RNA ends confirmed the expression and the termini of the newly predicted snoRNAs. Our study especially expanded on the current knowledge of box H/ACA snoRNAs and snoRNA species targeting snRNAs. In this study, we demonstrated that the use of small RNA sequencing data can increase the complexity and the accuracy of snoRNA annotation.

摘要

小核仁RNA(snoRNAs)是非编码RNA,可指导核糖体RNA或剪接体小核RNA上的2'-O-甲基化或假尿苷化。这些修饰对于调节核糖体和剪接体的活性是必需的。需要一份全面的snoRNA清单来扩展对这些修饰的认识。18 - 26个核苷酸的小RNA测序数据中与snoRNA对应的序列很少被探索,仍然是snoRNA注释的一个隐藏宝库。在这里,我们展示了拟南芥snoRNA末端小RNA的富集情况,并基于这一特征开发了一种计算方法来鉴定snoRNA。该方法成功地揭示了144个已知拟南芥snoRNA基因的全长序列,包括一些5'或3'端注释得到改进的snoRNA。此外,我们分别鉴定出27个和17个新型盒C/D和盒H/ACA snoRNA的候选序列。RNA末端平行分析的Northern印迹分析和测序数据证实了新预测的snoRNA的表达和末端。我们的研究特别扩展了当前关于盒H/ACA snoRNA和靶向snRNA的snoRNA种类的知识。在这项研究中,我们证明了使用小RNA测序数据可以提高snoRNA注释的复杂性和准确性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e85c/2685112/7a9217bcfd7c/gkp225f1.jpg

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