PRFdb: A database of computationally predicted eukaryotic programmed -1 ribosomal frameshift signals

BackgroundThe Programmed Ribosomal Frameshift Database (PRFdb) provides an interface to help researchers identify potential programmed -1 ribosomal frameshift (-1 PRF) signals in eukaryotic genes or sequences of interest.ResultsTo identify putative -1 PRF signals, sequences are first imported from whole genomes or datasets, e.g. the yeast genome project and mammalian gene collection. They are then filtered through multiple algorithms to identify potential -1 PRF signals as defined by a heptameric slippery site followed by an mRNA pseudoknot. The significance of each candidate -1 PRF signal is evaluated by comparing the predicted thermodynamic stability (ΔG°) of the native mRNA sequence against a distribution of ΔG° values of a pool of randomized sequences derived from the original. The data have been compiled in a user-friendly, easily searchable relational database.ConclusionThe PRFdB enables members of the research community to determine whether genes that they are investigating contain potential -1 PRF signals, and can be used as a metasource of information for cross referencing with other databases. It is available on the web at http://dinmanlab.umd.edu/prfdb.

[1]  J. Dinman,et al.  A programmed -1 ribosomal frameshift signal can function as a cis-acting mRNA destabilizing element. , 2004, Nucleic acids research.

[2]  H. Hoos,et al.  HotKnots: heuristic prediction of RNA secondary structures including pseudoknots. , 2005, RNA.

[3]  P. Farabaugh Programmed translational frameshifting. , 1996, Annual review of genetics.

[4]  Raymond F. Gesteland,et al.  RECODE: a database of frameshifting, bypassing and codon redefinition utilized for gene expression , 2001, Nucleic Acids Res..

[5]  J. F. Atkins,et al.  Recoding: dynamic reprogramming of translation. , 1996, Annual review of biochemistry.

[6]  Raymond F. Gesteland,et al.  Recode 2003 , 2003, Nucleic Acids Res..

[7]  H. Varmus,et al.  Expression of the Rous sarcoma virus pol gene by ribosomal frameshifting. , 1985, Science.

[8]  Sanghoon Moon,et al.  FSDB: A frameshift signal database , 2007, Computational Biology and Chemistry.

[9]  I. Brierley,et al.  Characterization of the frameshift signal of Edr, a mammalian example of programmed −1 ribosomal frameshifting , 2005, Nucleic acids research.

[10]  J. Sabina,et al.  Expanded sequence dependence of thermodynamic parameters improves prediction of RNA secondary structure. , 1999, Journal of molecular biology.

[11]  I. Brierley,et al.  Ribosomal frameshifting viral RNAs. , 1995, The Journal of general virology.

[12]  Niles A. Pierce,et al.  An algorithm for computing nucleic acid base‐pairing probabilities including pseudoknots , 2004, J. Comput. Chem..

[13]  Yanga Byun,et al.  PSEUDOVIEWER2: visualization of RNA pseudoknots of any type , 2003, Nucleic Acids Res..

[14]  E Rivas,et al.  A dynamic programming algorithm for RNA structure prediction including pseudoknots. , 1998, Journal of molecular biology.

[15]  Jonathan D. Dinman,et al.  Identification of functional, endogenous programmed −1 ribosomal frameshift signals in the genome of Saccharomyces cerevisiae , 2006, Nucleic acids research.

[16]  J. Dinman Programmed Ribosomal Frameshifting Goes Beyond Viruses: Organisms from all three kingdoms use frameshifting to regulate gene expression, perhaps signaling a paradigm shift. , 2006, Microbe.

[17]  D. Ecker,et al.  RNAMotif, an RNA secondary structure definition and search algorithm. , 2001, Nucleic acids research.

[18]  Michael B. Mathews,et al.  Translational control in biology and medicine , 2007 .

[19]  Chris M. Brown,et al.  Detecting overlapping coding sequences in virus genomes , 2006, BMC Bioinformatics.