Ribosomal Pausing at a Frameshifter RNA Pseudoknot Is Sensitive to Reading Phase but Shows Little Correlation with Frameshift Efficiency

ABSTRACT Here we investigated ribosomal pausing at sites of programmed −1 ribosomal frameshifting, using translational elongation and ribosome heelprint assays. The site of pausing at the frameshift signal of infectious bronchitis virus (IBV) was determined and was consistent with an RNA pseudoknot-induced pause that placed the ribosomal P- and A-sites over the slippery sequence. Similarly, pausing at the simian retrovirus 1 gag/pol signal, which contains a different kind of frameshifter pseudoknot, also placed the ribosome over the slippery sequence, supporting a role for pausing in frameshifting. However, a simple correlation between pausing and frameshifting was lacking. Firstly, a stem-loop structure closely related to the IBV pseudoknot, although unable to stimulate efficient frameshifting, paused ribosomes to a similar extent and at the same place on the mRNA as a parental pseudoknot. Secondly, an identical pausing pattern was induced by two pseudoknots differing only by a single loop 2 nucleotide yet with different functionalities in frameshifting. The final observation arose from an assessment of the impact of reading phase on pausing. Given that ribosomes advance in triplet fashion, we tested whether the reading frame in which ribosomes encounter an RNA structure (the reading phase) would influence pausing. We found that the reading phase did influence pausing but unexpectedly, the mRNA with the pseudoknot in the phase which gave the least pausing was found to promote frameshifting more efficiently than the other variants. Overall, these experiments support the view that pausing alone is insufficient to mediate frameshifting and additional events are required. The phase dependence of pausing may be indicative of an activity in the ribosome that requires an optimal contact with mRNA secondary structures for efficient unwinding.

[1]  W. Szer,et al.  Effect of edeine on aminoacyl-tRNA binding to ribosomes and its relationship to ribosomal binding sites. , 1970, Biochimica et biophysica acta.

[2]  C. Milcarek,et al.  The metabolism of a poly(A) minus mRNA fraction in HeLa cells. , 1974, Cell.

[3]  F. Sanger,et al.  DNA sequencing with chain-terminating inhibitors. , 1977, Proceedings of the National Academy of Sciences of the United States of America.

[4]  N. Zinder,et al.  Functional analysis of bacteriophage f1 intergenic region. , 1981, Virology.

[5]  M. Kozak Comparison of initiation of protein synthesis in procaryotes, eucaryotes, and organelles. , 1983, Microbiological reviews.

[6]  J. Sambrook,et al.  Molecular Cloning: A Laboratory Manual , 2001 .

[7]  D. Melton,et al.  Efficient in vitro synthesis of biologically active RNA and RNA hybridization probes from plasmids containing a bacteriophage SP6 promoter. , 1984, Nucleic acids research.

[8]  T. Kunkel Rapid and efficient site-specific mutagenesis without phenotypic selection. , 1985, Proceedings of the National Academy of Sciences of the United States of America.

[9]  S. Kidd,et al.  An improved filamentous helper phage for generating single-stranded plasmid DNA. , 1986, Gene.

[10]  C. Thomas Caskey,et al.  Translational frameshifting: Where will it stop? , 1987, Cell.

[11]  P. Walter,et al.  Ribosome pausing and stacking during translation of a eukaryotic mRNA. , 1988, The EMBO journal.

[12]  H. Varmus,et al.  Signals for ribosomal frameshifting in the rous sarcoma virus gag-pol region , 1988, Cell.

[13]  D. Glitz,et al.  Wheat germ cytoplasmic ribosomes. Structure of ribosomal subunits and localization of N6,N6-dimethyladenosine by immunoelectron microscopy. , 1988, The Journal of biological chemistry.

[14]  I. Brierley,et al.  Characterization of an efficient coronavirus ribosomal frameshifting signal: Requirement for an RNA pseudoknot , 1989, Cell.

[15]  W. Tate,et al.  Frameshift autoregulation in the gene for Escherichia coli release factor 2: partly functional mutants result in frameshift enhancement. , 1990, Nucleic acids research.

[16]  Z. Tsuchihashi,et al.  Translational frameshifting in the Escherichia coli dnaX gene in vitro. , 1991, Nucleic acids research.

[17]  I. Brierley,et al.  Mutational analysis of the RNA pseudoknot component of a coronavirus ribosomal frameshifting signal☆ , 1991, Journal of Molecular Biology.

[18]  I. Brierley,et al.  Mutational analysis of the “slippery-sequence” component of a coronavirus ribosomal frameshifting signal , 1992, Journal of Molecular Biology.

[19]  J A Bruenn,et al.  Ribosomal movement impeded at a pseudoknot required for frameshifting. , 1992, Proceedings of the National Academy of Sciences of the United States of America.

[20]  S. Harrison,et al.  Long-COVID Symptoms in Individuals Infected with Different SARS-CoV-2 Variants of Concern: A Systematic Review of the Literature , 2022, Viruses.

[21]  J. P. Doohan,et al.  Biosynthesis of reovirus-specified polypeptides: ribosome pausing during the translation of reovirus S1 mRNA. , 1992, Virology.

[22]  R. Wickner,et al.  Ribosomal frameshifting efficiency and gag/gag-pol ratio are critical for yeast M1 double-stranded RNA virus propagation , 1992, Journal of virology.

[23]  I. Brierley,et al.  Ribosomal pausing during translation of an RNA pseudoknot , 1993, Molecular and cellular biology.

[24]  C. Pleij,et al.  Identification and analysis of the pseudoknot-containing gag-pro ribosomal frameshift signal of simian retrovirus-1. , 1994, Nucleic acids research.

[25]  J. Dinman Ribosomal frameshifting in yeast viruses , 1995, Yeast.

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

[27]  H. Varmus,et al.  Structural and functional studies of retroviral RNA pseudoknots involved in ribosomal frameshifting: nucleotides at the junction of the two stems are important for efficient ribosomal frameshifting. , 1995, The EMBO journal.

[28]  C. Pleij,et al.  Analysis of the role of the pseudoknot component in the SRV-1 gag-pro ribosomal frameshift signal: loop lengths and stability of the stem regions. , 1995, RNA.

[29]  I. Tinoco,et al.  The structure of an RNA pseudoknot that causes efficient frameshifting in mouse mammary tumor virus. , 1995, Journal of molecular biology.

[30]  H. Varmus,et al.  A characteristic bent conformation of RNA pseudoknots promotes -1 frameshifting during translation of retroviral RNA. , 1996, Journal of molecular biology.

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

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

[33]  D. Giedroc,et al.  Base-pairings within the RNA pseudoknot associated with the simian retrovirus-1 gag-pro frameshift site. , 1997, Journal of molecular biology.

[34]  D. Sung,et al.  Mutational analysis of the RNA pseudoknot involved in efficient ribosomal frameshifting in simian retrovirus-1. , 1998, Nucleic acids research.

[35]  S. Napthine,et al.  The role of RNA pseudoknot stem 1 length in the promotion of efficient −1 ribosomal frameshifting 1 , 1999, Journal of Molecular Biology.

[36]  J. F. Atkins,et al.  Structural studies of the RNA pseudoknot required for readthrough of the gag-termination codon of murine leukemia virus. , 1999, Journal of molecular biology.

[37]  A. Böck,et al.  Dynamics and efficiency in vivo of UGA‐directed selenocysteine insertion at the ribosome , 1999, The EMBO journal.

[38]  J. Berger,et al.  Minor groove RNA triplex in the crystal structure of a ribosomal frameshifting viral pseudoknot , 1999, Nature Structural Biology.

[39]  S. Napthine,et al.  Evidence for an RNA pseudoknot loop-helix interaction essential for efficient −1 ribosomal frameshifting 1 , 1999, Journal of Molecular Biology.

[40]  P. Farabaugh,et al.  How translational accuracy influences reading frame maintenance , 1999, The EMBO journal.

[41]  P. Farabaugh Translational frameshifting: implications for the mechanism of translational frame maintenance. , 2000, Progress in nucleic acid research and molecular biology.

[42]  Jonathan D. Dinman,et al.  Kinetics of Ribosomal Pausing during Programmed −1 Translational Frameshifting , 2000, Molecular and Cellular Biology.

[43]  R. Gesteland,et al.  One protein from two open reading frames: mechanism of a 50 nt translational bypass , 2000, The EMBO journal.

[44]  I. Brierley,et al.  The Q-base of asparaginyl-tRNA is dispensable for efficient −1 ribosomal frameshifting in eukaryotes1 , 2000, Journal of Molecular Biology.

[45]  C. W. Hilbers,et al.  Solution structure of the pseudoknot of SRV-1 RNA, involved in ribosomal frameshifting1 , 2001, Journal of Molecular Biology.

[46]  P. Farabaugh,et al.  Programmed +1 frameshifting stimulated by complementarity between a downstream mRNA sequence and an error-correcting region of rRNA. , 2001, RNA.