Nucleic Acids Research, 1995, Vol. 23, No. 14 2791-2798
© 1995
RNA |
Well-determined regions in RNA secondary structure prediction: analysis of small subunit ribosomal RNA
Institute for Biomedical Computing, Washington University St Louis, MO 63110, USA 1Department of Microbiology, State University of New York Stony Brook, NY 11794-5222, USA
*To whom correspondence should be addressed
Received January 6, 1995. Accepted May 10, 1995.
Recent structural analyses of genomic RNAs from RNA coliphages suggest that both well-determined base paired helices and well-determined structural domains that are identified by energy dot plot analysis using the RNA folding package mfold, are likely to be predicted correctly. To test these observations with another group of large RNAs, we have analyzed 15 ribosomal RNAs. Published secondary structure models that were derived by comparative sequence analysis were used to evaluate the predicted structures. Both the optimal predicted fold and the predicted energy dot plot of each sequence were examined. Each prediction was obtained from a single computer run on an entire ribosomal RNA sequence. All predicted base pairs in optimal foldings were examined for agreement with proven base pairs in the comparative models. Our analyses show that the overall correspondence between the predicted and comparative models varies for different RNAs and ranges from a low of 27% to a high of 70%, with a mean value of 49%. The correspondence improves to a mean value of 81% when the analysis is limited to welldetermined helices. In addition to well-determined helices, large well-determined structural domains can be observed in energy dot plots of some 16S ribosomal RNAs. The predicted domains correspond closely with structural domains that are found by the comparative method in the same RNAs. Our analyses also show that measuring the agreement between predicted and comparative secondary structure models underestimates the reliability of structural prediction by mfold.
![]()
CiteULike
Connotea
Del.icio.us What's this?
This article has been cited by other articles:
![]() |
D. A. Defenbaugh, M. Johnson, R. Chen, Y. Y. Zheng, and J. L. Casey Hepatitis Delta Antigen Requires a Minimum Length of the Hepatitis Delta Virus Unbranched Rod RNA Structure for Binding J. Virol., May 1, 2009; 83(9): 4548 - 4556. [Abstract] [Full Text] [PDF] |
||||
![]() |
C. A. Dumstorf, S. Mukhopadhyay, E. Krishnan, B. Haribabu, and W. G. McGregor REV1 Is Implicated in the Development of Carcinogen-Induced Lung Cancer Mol. Cancer Res., February 1, 2009; 7(2): 247 - 254. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. A. MIR and A. T. PANGANIBAN The bunyavirus nucleocapsid protein is an RNA chaperone: Possible roles in viral RNA panhandle formation and genome replication RNA, February 1, 2006; 12(2): 272 - 282. [Abstract] [Full Text] [PDF] |
||||
![]() |
D. H. Mathews Predicting a set of minimal free energy RNA secondary structures common to two sequences Bioinformatics, May 15, 2005; 21(10): 2246 - 2253. [Abstract] [Full Text] [PDF] |
||||
![]() |
G. Ghazal, D. Ge, J. Gervais-Bird, J. Gagnon, and S. Abou Elela Genome-Wide Prediction and Analysis of Yeast RNase III-Dependent snoRNA Processing Signals Mol. Cell. Biol., April 15, 2005; 25(8): 2981 - 2994. [Abstract] [Full Text] [PDF] |
||||
![]() |
D. M. Layton and R. Bundschuh A statistical analysis of RNA folding algorithms through thermodynamic parameter perturbation Nucleic Acids Res., January 26, 2005; 33(2): 519 - 524. [Abstract] [Full Text] [PDF] |
||||
![]() |
D. H. MATHEWS Using an RNA secondary structure partition function to determine confidence in base pairs predicted by free energy minimization RNA, August 1, 2004; 10(8): 1178 - 1190. [Abstract] [Full Text] [PDF] |
||||
![]() |
D. R. Clark, W. Zacharias, L. Panaitescu, and W. G. McGregor Ribozyme-mediated REV1 inhibition reduces the frequency of UV-induced mutations in the human HPRT gene Nucleic Acids Res., September 1, 2003; 31(17): 4981 - 4988. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. Gabler, S. Krebs, D. Seichter, and M. Forster Fast and accurate determination of sites along the FUT2 in vitro transcript that are accessible to antisense oligonucleotides by application of secondary structure predictions and RNase H in combination with MALDI-TOF mass spectrometry Nucleic Acids Res., August 1, 2003; 31(15): e79 - e79. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. Zuker Mfold web server for nucleic acid folding and hybridization prediction Nucleic Acids Res., July 1, 2003; 31(13): 3406 - 3415. [Abstract] [Full Text] [PDF] |
||||
![]() |
I. L. Hofacker Vienna RNA secondary structure server Nucleic Acids Res., July 1, 2003; 31(13): 3429 - 3431. [Abstract] [Full Text] [PDF] |
||||
![]() |
Y.-J. Hu GPRM: a genetic programming approach to finding common RNA secondary structure elements Nucleic Acids Res., July 1, 2003; 31(13): 3446 - 3449. [Abstract] [Full Text] [PDF] |
||||
![]() |
H. H. Gan, S. Pasquali, and T. Schlick Exploring the repertoire of RNA secondary motifs using graph theory; implications for RNA design Nucleic Acids Res., June 1, 2003; 31(11): 2926 - 2943. [Abstract] [Full Text] [PDF] |
||||
![]() |
H. Duque and A. C. Palmenberg Phenotypic Characterization of Three Phylogenetically Conserved Stem-Loop Motifs in the Mengovirus 3' Untranslated Region J. Virol., April 1, 2001; 75(7): 3111 - 3120. [Abstract] [Full Text] |
||||
![]() |
Y. Ding and C. E. Lawrence Statistical prediction of single-stranded regions in RNA secondary structure and application to predicting effective antisense target sites and beyond Nucleic Acids Res., March 1, 2001; 29(5): 1034 - 1046. [Abstract] [Full Text] [PDF] |
||||
![]() |
J.-H. Chen, S.-Y. Le, and J. V. Maizel Prediction of common secondary structures of RNAs: a genetic algorithm approach Nucleic Acids Res., February 15, 2000; 28(4): 991 - 999. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. Hersberger, S. Patarroyo-White, K. S. Arnold, and T. L. Innerarity Phylogenetic Analysis of the Apolipoprotein B mRNA-editing Region. EVIDENCE FOR A SECONDARY STRUCTURE BETWEEN THE MOORING SEQUENCE AND THE 3' EFFICIENCY ELEMENT J. Biol. Chem., December 3, 1999; 274(49): 34590 - 34597. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. M. Aschoff, D. Foster, and J. M. Coffin Point Mutations in the Avian Sarcoma/Leukosis Virus 3' Untranslated Region Result in a Packaging Defect J. Virol., September 1, 1999; 73(9): 7421 - 7429. [Abstract] [Full Text] |
||||
![]() |
H. Ulrich, J. E. Ippolito, O. R. Pagan, V. A. Eterovic, R. M. Hann, H. Shi, J. T. Lis, M. E. Eldefrawi, and G. P. Hess In vitro selection of RNA molecules that displace cocaine from the membrane-bound nicotinic acetylcholine receptor PNAS, November 24, 1998; 95(24): 14051 - 14056. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. Hersberger and T. L. Innerarity Two Efficiency Elements Flanking the Editing Site of Cytidine 6666 in the Apolipoprotein B mRNA Support Mooring-dependent Editing J. Biol. Chem., April 17, 1998; 273(16): 9435 - 9442. [Abstract] [Full Text] [PDF] |
||||
![]() |
M P Playford, R J Butler, X C Wang, R M Katso, I E Cooke, and T S Ganesan The genomic structure of discoidin receptor tyrosine kinase. Genome Res., July 1, 1996; 6(7): 620 - 627. [Abstract] [PDF] |
||||








