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

被引:99
作者
Duarte, CM
Wadley, LM
Pyle, AM
机构
[1] Yale Univ, Dept Mol Biophys & Biochem, New Haven, CT 06520 USA
[2] Columbia Univ, Dept Biochem & Mol Biophys, New York, NY 10032 USA
[3] Columbia Univ, Dept Phys, New York, NY 10027 USA
[4] Yale Univ, Howard Hughes Med Inst, New Haven, CT 06520 USA
关键词
D O I
10.1093/nar/gkg682
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页码:4755 / 4761
页数:7
相关论文
共 39 条
[1]   The complete atomic structure of the large ribosomal subunit at 2.4 Å resolution [J].
Ban, N ;
Nissen, P ;
Hansen, J ;
Moore, PB ;
Steitz, TA .
SCIENCE, 2000, 289 (5481) :905-920
[2]   THE NUCLEIC-ACID DATABASE - A COMPREHENSIVE RELATIONAL DATABASE OF 3-DIMENSIONAL STRUCTURES OF NUCLEIC-ACIDS [J].
BERMAN, HM ;
OLSON, WK ;
BEVERIDGE, DL ;
WESTBROOK, J ;
GELBIN, A ;
DEMENY, T ;
HSIEH, SH ;
SRINIVASAN, AR ;
SCHNEIDER, B .
BIOPHYSICAL JOURNAL, 1992, 63 (03) :751-759
[3]   The Protein Data Bank [J].
Berman, HM ;
Westbrook, J ;
Feng, Z ;
Gilliland, G ;
Bhat, TN ;
Weissig, H ;
Shindyalov, IN ;
Bourne, PE .
NUCLEIC ACIDS RESEARCH, 2000, 28 (01) :235-242
[4]   The structural basis for the action of the antibiotics tetracycline, pactamycin, and hygromycin B on the 30S ribosomal subunit [J].
Brodersen, DE ;
Clemons, WM ;
Carter, AP ;
Morgan-Warren, RJ ;
Wimberly, BT ;
Ramakrishnan, V .
CELL, 2000, 103 (07) :1143-1154
[5]   The two faces of the Escherichia coli 23 S rRNA sarcin/ricin domain:: The structure at 1.11 Å resolution [J].
Correll, CC ;
Wool, IG ;
Munishkin, A .
JOURNAL OF MOLECULAR BIOLOGY, 1999, 292 (02) :275-287
[6]   Stepping through an RNA structure: A novel approach to conformational analysis [J].
Duarte, CM ;
Pyle, AM .
JOURNAL OF MOLECULAR BIOLOGY, 1998, 284 (05) :1465-1478
[7]   The crystal structure of UUCG tetraloop [J].
Ennifar, E ;
Nikulin, A ;
Tishchenko, S ;
Serganov, A ;
Nevskaya, N ;
Garber, M ;
Ehresmann, B ;
Ehresmann, C ;
Nikonov, S ;
Dumas, P .
JOURNAL OF MOLECULAR BIOLOGY, 2000, 304 (01) :35-42
[8]   Ribosomal dynamics explored by cryo-electron microscopy [J].
Frank, J .
METHODS, 2001, 25 (03) :309-315
[9]   Reconstitution of functional 50S ribosomes from in vitro transcripts of Bacillus stearothermophilus 23S rRNA [J].
Green, R ;
Noller, HF .
BIOCHEMISTRY, 1999, 38 (06) :1772-1779
[10]  
Hutchinson EG, 1996, PROTEIN SCI, V5, P212