Conserved RNA secondary structures in Picornaviridae genomes.

The family Picornaviridae contains important pathogens including, for example, hepatitis A virus and foot-and-mouth disease virus. The genome of these viruses is a single messenger-active (+)-RNA of 7200-8500 nt. Besides coding for the viral proteins, it also contains functionally important RNA secondary structures, among them an internal ribosomal entry site (IRES) region towards the 5'-end. This contribution provides a comprehensive computational survey of the complete genomic RNAs and a detailed comparative analysis of the conserved structural elements in seven of the currently nine genera in the family PICORNAVIRIDAE: Compared with previous studies we find: (i) that only smaller sections of the IRES region than previously reported are conserved at single base-pair resolution and (ii) that there is a number of significant structural elements in the coding region. Furthermore, we identify potential cis-acting replication elements in four genera where this feature has not been reported so far.

[1]  E. Wimmer,et al.  The 5' end of poliovirus mRNA is not capped with m7G(5')ppp(5')Np. , 1976, Proceedings of the National Academy of Sciences of the United States of America.

[2]  D. Baltimore,et al.  5'-terminal structure of poliovirus polyribosomal RNA is pUp. , 1976, Proceedings of the National Academy of Sciences of the United States of America.

[3]  D. Sankoff Simultaneous Solution of the RNA Folding, Alignment and Protosequence Problems , 1985 .

[4]  B. Clarke,et al.  Potential secondary and tertiary structure in the genomic RNA of foot and mouth disease virus. , 1987, Nucleic acids research.

[5]  V. Blinov,et al.  Conserved structural domains in the 5'-untranslated region of picornaviral genomes: an analysis of the segment controlling translation and neurovirulence. , 1989, Virology.

[6]  T. M. Dmitrieva,et al.  Conservation of the secondary structure elements of the 5'-untranslated region of cardio- and aphthovirus RNAs. , 1989, Nucleic acids research.

[7]  Daniel Gautheret,et al.  Pattern searching/alignment with RNA primary and secondary structures: an effective descriptor for tRNA , 1990, Comput. Appl. Biosci..

[8]  R. Jackson,et al.  The novel mechanism of initiation of picornavirus RNA translation. , 1990, Trends in biochemical sciences.

[9]  M. Zuker,et al.  Common structures of the 5' non-coding RNA in enteroviruses and rhinoviruses. Thermodynamical stability and statistical significance. , 1990, Journal of molecular biology.

[10]  J. McCaskill The equilibrium partition function and base pair binding probabilities for RNA secondary structure , 1990, Biopolymers.

[11]  M. Zuker,et al.  Predicting common foldings of homologous RNAs. , 1991, Journal of biomolecular structure & dynamics.

[12]  S. Lemon,et al.  The 5' nontranslated region of hepatitis A virus RNA: secondary structure and elements required for translation in vitro , 1991, Journal of virology.

[13]  V. Agol,et al.  Towards identification of cis-acting elements involved in the replication of enterovirus and rhinovirus RNAs: a proposal for the existence of tRNA-like terminal structures. , 1992, Nucleic acids research.

[14]  M. Hoffman,et al.  Sequence and structural elements that contribute to efficient encephalomyocarditis virus RNA translation , 1992, Journal of virology.

[15]  S Y Le,et al.  Conserved tertiary structural elements in the 5' nontranslated region of cardiovirus, aphthovirus and hepatitis A virus RNAs. , 1993, Nucleic acids research.

[16]  P. Schuster,et al.  Statistics of RNA secondary structures , 1993, Biopolymers.

[17]  M. Zuker,et al.  Structural analysis by energy dot plot of a large mRNA. , 1993, Journal of molecular biology.

[18]  Walter Fontana,et al.  Fast folding and comparison of RNA secondary structures , 1994 .

[19]  P. Schuster,et al.  From sequences to shapes and back: a case study in RNA secondary structures , 1994, Proceedings of the Royal Society of London. Series B: Biological Sciences.

[20]  J. Thompson,et al.  CLUSTAL W: improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choice. , 1994, Nucleic acids research.

[21]  M. Hentze,et al.  Finding the hairpin in the haystack: searching for RNA motifs. , 1995, Trends in genetics : TIG.

[22]  D. H. Moon,et al.  The 3' untranslated region of picornavirus RNA: features required for efficient genome replication , 1995, Journal of virology.

[23]  A. Porter,et al.  Localization of binding site for encephalomyocarditis virus RNA polymerase in the 3'-noncoding region of the viral RNA. , 1995, Nucleic acids research.

[24]  H. Auer,et al.  Equine rhinovirus serotypes 1 and 2: relationship to each other and to aphthoviruses and cardioviruses. , 1996, The Journal of general virology.

[25]  R. Lück,et al.  Thermodynamic prediction of conserved secondary structure: application to the RRE element of HIV, the tRNA-like element of CMV and the mRNA of prion protein. , 1996, Journal of molecular biology.

[26]  G. Stanway,et al.  An RNA tertiary structure in the 3' untranslated region of enteroviruses is necessary for efficient replication , 1997, Journal of virology.

[27]  N. Moscufo,et al.  Encapsidation of Viral Rna. Poliovirus 2c Region Functions During , 1997 .

[28]  R. Zell,et al.  Application of genome sequence information to the classification of bovine enteroviruses: the importance of 5'- and 3'-nontranslated regions. , 1997, Virus research.

[29]  A. Palmenberg,et al.  TOPOLOGICAL ORGANIZATION OF PICORNAVIRAL GENOMES : STATISTICAL PREDICTION OF RNA STRUCTURAL SIGNALS , 1997 .

[30]  Peter F. Stadler,et al.  Spontaneous and Engineered Deletions in the 3′ Noncoding Region of Tick-Borne Encephalitis Virus: Construction of Highly Attenuated Mutants of a Flavivirus , 1998, Journal of Virology.

[31]  M. Pallansch,et al.  Complete sequence of echovirus 23 and its relationship to echovirus 22 and other human enteroviruses. , 1998, Virus research.

[32]  S. Lemon,et al.  The rhinovirus type 14 genome contains an internally located RNA structure that is required for viral replication. , 1998, RNA.

[33]  T. Hyypiä,et al.  Molecular analysis of human parechovirus type 2 (formerly echovirus 23). , 1998, The Journal of general virology.

[34]  M. Huynen,et al.  Automatic detection of conserved RNA structure elements in complete RNA virus genomes. , 1998, Nucleic acids research.

[35]  FOOT-AND-MOUTH DISEASE VIRUSES (PICORNAVIRIDAE) , 1999 .

[36]  Peter F. Stadler,et al.  Conserved secondary structures in hepatitis B virus DNA , 1999, German Conference on Bioinformatics.

[37]  N. Escriou,et al.  A coding RNA sequence acts as a replication signal in cardioviruses. , 1999, Proceedings of the National Academy of Sciences of the United States of America.

[38]  V. Juan,et al.  RNA secondary structure prediction based on free energy and phylogenetic analysis. , 1999, Journal of molecular biology.

[39]  N. Mcferran,et al.  Sequence analysis of a porcine enterovirus serotype 1 isolate: relationships with other picornaviruses. , 1999, The Journal of general virology.

[40]  Peter F. Stadler,et al.  Automatic Detection of Conserved Base Pairing Patterns in RNA Virus Genomes , 1998, Comput. Chem..

[41]  J. Meredith,et al.  Similar Interactions of the Poliovirus and Rhinovirus 3D Polymerases with the 3′ Untranslated Region of Rhinovirus 14 , 1999, Journal of Virology.

[42]  R. Lück,et al.  ConStruct: a tool for thermodynamic controlled prediction of conserved secondary structure. , 1999, Nucleic acids research.

[43]  V. Agol,et al.  Structural requirements of the higher order RNA kissing element in the enteroviral 3'UTR. , 1999, Nucleic acids research.

[44]  J. Meredith,et al.  Identification of a cis-Acting Replication Element within the Poliovirus Coding Region , 2000, Journal of Virology.

[45]  J. Doudna Structural genomics of RNA , 2000, Nature Structural Biology.

[46]  N. Suzuki Virus Taxonomy : Seventh Report of the International Committee for the Taxonomy of Viruses.(共著) , 2000 .

[47]  V. Racaniello Picornaviridae : the viruses and their replication , 2001 .

[48]  A. Palmenberg,et al.  Phenotypic Characterization of Three Phylogenetically Conserved Stem-Loop Motifs in the Mengovirus 3′ Untranslated Region , 2001, Journal of Virology.

[49]  R. Zell,et al.  Porcine Teschoviruses Comprise at Least Eleven Distinct Serotypes: Molecular and Evolutionary Aspects , 2001, Journal of Virology.