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本文引用的文献

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The kink-turn: a new RNA secondary structure motif.扭结转角:一种新的RNA二级结构基序。
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利用RNA构象空间的简化表示进行RNA结构比较、基序搜索与发现。

RNA structure comparison, motif search and discovery using a reduced representation of RNA conformational space.

作者信息

Duarte Carlos M, Wadley Leven M, Pyle Anna Marie

机构信息

Department of Biochemistry and Molecular Biophysics, Columbia University, New York, NY 10032, USA.

出版信息

Nucleic Acids Res. 2003 Aug 15;31(16):4755-61. doi: 10.1093/nar/gkg682.

DOI:10.1093/nar/gkg682
PMID:12907716
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC169959/
Abstract

Given the wealth of new RNA structures and the growing list of RNA functions in biology, it is of great interest to understand the repertoire of RNA folding motifs. The ability to identify new and known motifs within novel RNA structures, to compare tertiary structures with one another and to quantify the characteristics of a given RNA motif are major goals in the field of RNA research; however, there are few systematic ways to address these issues. Using a novel approach for visualizing and mathematically describing macromolecular structures, we have developed a means to quantitatively describe RNA molecules in order to rapidly analyze, compare and explore their features. This approach builds on the alternative eta,theta convention for describing RNA torsion angles and is executed using a new program called PRIMOS. Applying this methodology, we have successfully identified major regions of conformational change in the 50S and 30S ribosomal subunits, we have developed a means to search the database of RNA structures for the prevalence of known motifs and we have classified and identified new motifs. These applications illustrate the powerful capabilities of our new RNA structural convention, and they suggest future adaptations with important implications for bioinformatics and structural genomics.

摘要

鉴于新的RNA结构丰富多样,且RNA在生物学中的功能列表不断增加,了解RNA折叠基序的全部内容具有极大的意义。在新的RNA结构中识别新的和已知的基序、相互比较三级结构以及量化给定RNA基序的特征,这些能力是RNA研究领域的主要目标;然而,几乎没有系统的方法来解决这些问题。我们采用一种可视化和数学描述大分子结构的新方法,开发了一种定量描述RNA分子的手段,以便快速分析、比较和探索它们的特征。这种方法基于描述RNA扭转角的替代eta、theta约定,并使用一个名为PRIMOS的新程序来执行。应用这种方法,我们成功地识别了50S和30S核糖体亚基构象变化的主要区域,我们开发了一种方法来在RNA结构数据库中搜索已知基序的普遍性,并且我们对新基序进行了分类和识别。这些应用展示了我们新的RNA结构约定的强大功能,并且它们暗示了未来的适应性,这对生物信息学和结构基因组学具有重要意义。