Pseudoknots in prion protein mRNAs confirmed by comparative sequence analysis and pattern searching.

The human prion gene contains five copies of a 24 nt repeat that is highly conserved among species. An analysis of folding free energies of the human prion mRNA, in particular in the repeat region, suggested biased codon selection and the presence of RNA patterns. In particular, pseudoknots, similar to the one predicted by Wills in the human prion mRNA, were identified in the repeat region of all available prion mRNAs available in GenBank, but not those of birds and the red slider turtle. An alignment of these mRNAs, which share low sequence homology, shows several co-variations that maintain the pseudoknot pattern. The presence of pseudoknots in yeast Sup35p and Rnq1 suggests acquisition in the prokaryotic era. Computer generated three-dimensional structures of the human prion pseudoknot highlight protein and RNA interaction domains, which suggest a possible effect in prion protein translation. The role of pseudoknots in prion diseases is discussed as individuals with extra copies of the 24 nt repeat develop the familial form of Creutzfeldt-Jakob disease.

[1]  Peter R. Wills,et al.  Stem loops in hiv and prion protein messenger-RNAS , 1990 .

[2]  S. Lindquist,et al.  Rnq1: an epigenetic modifier of protein function in yeast. , 2000, Molecular cell.

[3]  D. Goldgaber,et al.  Transmissible familial Creutzfeldt-Jakob disease associated with five, seven, and eight extra octapeptide coding repeats in the PRNP gene. , 1991, Proceedings of the National Academy of Sciences of the United States of America.

[4]  R. Casareno,et al.  Brain Copper Content and Cuproenzyme Activity Do Not Vary with Prion Protein Expression Level* , 2000, The Journal of Biological Chemistry.

[5]  M. Karplus,et al.  CHARMM: A program for macromolecular energy, minimization, and dynamics calculations , 1983 .

[6]  R. Wagner,et al.  5S RNA structure and function. , 1988, Methods in enzymology.

[7]  B. Ghetti,et al.  Neurological Illness in Transgenic Mice Expressing a Prion Protein with an Insertional Mutation , 1998, Neuron.

[8]  L. Defebvre,et al.  Prominent psychiatric features and early onset in an inherited prion disease with a new insertional mutation in the prion protein gene. , 1999, Brain : a journal of neurology.

[9]  E. Wagner,et al.  Antisense RNA regulation in prokaryotes: rapid RNA/RNA interaction facilitated by a general U-turn loop structure. , 1999, Journal of molecular biology.

[10]  Jan van Duin,et al.  Control of prokaryotic translational initiation by mRNA secondary structure , 1990 .

[11]  G. Bannon,et al.  mRNA stability plays a major role in regulating the temperature-specific expression of a Tetrahymena thermophila surface protein , 1988, Molecular and cellular biology.

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

[13]  G Lapalme,et al.  The combination of symbolic and numerical computation for three-dimensional modeling of RNA. , 1991, Science.

[14]  S. Prusiner,et al.  A transmembrane form of the prion protein in neurodegenerative disease. , 1998, Science.

[15]  F. Cohen,et al.  Eight prion strains have PrPSc molecules with different conformations , 1998, Nature Medicine.

[16]  J. Collinge,et al.  Prion protein gene analysis in new variant cases of Creutzfeldt-Jakob disease , 1996, The Lancet.

[17]  S. Le,et al.  A method for assessing the statistical significance of RNA folding. , 1989, Journal of theoretical biology.

[18]  Alexander D. MacKerell,et al.  All-atom empirical potential for molecular modeling and dynamics studies of proteins. , 1998, The journal of physical chemistry. B.

[19]  B. Ghetti,et al.  Accumulation of protease-resistant prion protein (PrP) and apoptosis of cerebellar granule cells in transgenic mice expressing a PrP insertional mutation. , 2000, Proceedings of the National Academy of Sciences of the United States of America.

[20]  P. Wills Potential pseudoknots in the PrP-encoding mRNA. , 1992, Journal of theoretical biology.

[21]  David W. Digby,et al.  mRNAs have greater negative folding free energies than shuffled or codon choice randomized sequences. , 1999, Nucleic acids research.

[22]  U. Scheffer,et al.  Interaction of 68-kDa TAR RNA-binding protein and other cellular proteins with prion protein-RNA stem-loop. , 1995, Journal of neurovirology.

[23]  D. Draper,et al.  Pseudoknots, RNA Folding, and Translational Regulation , 1998 .

[24]  S. Lindquist,et al.  Oligopeptide-repeat expansions modulate ‘protein-only’ inheritance in yeast , 1999, Nature.

[25]  T. Werner,et al.  Analysis of 27 mammalian and 9 avian PrPs reveals high conservation of flexible regions of the prion protein. , 1999, Journal of molecular biology.

[26]  S. Duga,et al.  cDNA cloning of turtle prion protein , 2000, FEBS letters.

[27]  D. Forsdyke,et al.  A stem-loop "kissing" model for the initiation of recombination and the origin of introns. , 1995, Molecular biology and evolution.

[28]  E Westhof,et al.  Non-Watson-Crick base pairs in RNA-protein recognition. , 1999, Chemistry & biology.

[29]  L. R. Scott,et al.  Electrostatics and diffusion of molecules in solution: simulations with the University of Houston Brownian dynamics program , 1995 .

[30]  D Gautheret,et al.  Predicting U-turns in ribosomal RNA with comparative sequence analysis. , 2000, Journal of molecular biology.

[31]  E. Myers,et al.  Basic local alignment search tool. , 1990, Journal of molecular biology.

[32]  P R Wills,et al.  Stem loops in HIV and prion protein mRNAs. , 1990, Journal of acquired immune deficiency syndromes.

[33]  K R Williams,et al.  Translational repression by the bacteriophage T4 gene 32 protein involves specific recognition of an RNA pseudoknot structure. , 1993, Journal of molecular biology.

[34]  P Argos,et al.  Protein secondary structural types are differentially coded on messenger RNA , 1996, Protein science : a publication of the Protein Society.

[35]  H. Kretzschmar,et al.  Prion disease associated with a novel nine octapeptide repeat insertion in the PRNP gene. , 1995, Brain research. Molecular brain research.

[36]  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.

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

[38]  D. Westaway,et al.  The cellular prion protein binds copper in vivo , 1997, Nature.

[39]  J. van Duin,et al.  Control of prokaryotic translational initiation by mRNA secondary structure. , 1990, Progress in nucleic acid research and molecular biology.