4.4 Article

Analysis and classification of RNA tertiary structures

期刊

RNA
卷 14, 期 11, 页码 2274-2289

出版社

COLD SPRING HARBOR LAB PRESS, PUBLICATIONS DEPT
DOI: 10.1261/rna.853208

关键词

noncoding RNA; structural classification of RNA; alignment of RNA tertiary (3D) structures; 3D database search; edit distance of RNA secondary (2D) structures; RNA sequence comparison

资金

  1. Israeli Ministry of Science
  2. Israel Science Foundation [281/05]
  3. Hermann Minkowski-Minerva Center
  4. NIAID
  5. NIH [1UC1AI067231]
  6. Binational U.S.-Israel Science Foundation (BSF)
  7. National Cancer Institute
  8. Center for Cancer Research
  9. [N01-CO-12400]

向作者/读者索取更多资源

There is a fast growing interest in noncoding RNA transcripts. These transcripts are not translated into proteins, but play essential roles in many cellular and pathological processes. Recent efforts toward comprehension of their function has led to a substantial increase in both the number and the size of solved RNA structures. With the aim of addressing questions relating to RNA structural diversity, we examined RNA conservation at three structural levels: primary, secondary, and tertiary structure. Additionally, we developed an automated method for classifying RNA structures based on spatial (three-dimensional [3D]) similarity. Applying the method to all solved RNA structures resulted in a classified database of RNA tertiary structures (DARTS). DARTS embodies 1333 solved RNA structures classified into 94 clusters. The classification is hierarchical, reflecting the structural relationship between and within clusters. We also developed an application for searching DARTS with a new structure. The search is fast and its performance was successfully tested on all solved RNA structures since the creation of DARTS. A user-friendly interface for both the database and the search application is available online. We show intracluster and intercluster similarities in DARTS and demonstrate the usefulness of the search application. The analysis reveals the current structural repertoire of RNA and exposes common global folds and local tertiary motifs. Further study of these conserved substructures may suggest possible RNA domains and building blocks. This should be beneficial for structure prediction and for gaining insights into structure - function relationships.

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