Genetic code ambiguity: an unexpected source of proteome innovation and phenotypic diversity.

Translation of the genome into the proteome is a highly accurate biological process. However, the molecular mechanisms involved in protein synthesis are not error free and downstream protein quality control systems are needed to counteract the negative effects of translational errors (mistranslation) on proteome and cell homeostasis. This plus human and mice diseases caused by translational error generalized the idea that codon ambiguity is detrimental to life. Here we depart from this classical view of deleterious translational error and highlight how codon ambiguity can play important roles in the evolution of novel proteins. We also explain how tRNA mischarging can be relevant for the synthesis of functional proteomes, how codon ambiguity generates phenotypic and genetic diversity and how advantageous phenotypes can be selected, fixed, and inherited. A brief introduction to the molecular nature of translational error is provided; however, detailed information on the mechanistic aspects of mistranslation or comprehensive literature reviews of this topic should be obtained elsewhere.

[1]  M. Tuite,et al.  Transfer RNA structural change is a key element in the reassignment of the CUG codon in Candida albicans. , 1996, The EMBO journal.

[2]  Manuel A. S. Santos,et al.  A genetic code alteration generates a proteome of high diversity in the human pathogen Candida albicans , 2007, Genome Biology.

[3]  M. Z. Humayun,et al.  Escherichia coli cells bearing mutA, a mutant glyV tRNA gene, express a recA‐dependent error‐prone DNA replication activity , 1999, Molecular microbiology.

[4]  M. Wilcox Gamma-phosphoryl ester of glu-tRNA-GLN as an intermediate in Bacillus subtilis glutaminyl-tRNA synthesis. , 1969, Cold Spring Harbor symposia on quantitative biology.

[5]  J. Parker,et al.  Mistranslation during phenylalanine starvation , 1986, Molecular and General Genetics MGG.

[6]  Manuel A. S. Santos,et al.  Selective advantages created by codon ambiguity allowed for the evolution of an alternative genetic code in Candida spp. , 1999, Molecular microbiology.

[7]  M. Z. Humayun,et al.  Expression of mutant alanine tRNAs increases spontaneous mutagenesis in Escherichia coli , 2002, Molecular microbiology.

[8]  J. Parker,et al.  Context specific misreading of phenylalanine codons , 1989, Molecular and General Genetics MGG.

[9]  Sergey V. Balashov,et al.  Mistranslation induced by streptomycin provokes a RecABC/RuvABC-dependent mutator phenotype in Escherichia coli cells. , 2002, Journal of molecular biology.

[10]  A. Krol,et al.  The selenium to selenoprotein pathway in eukaryotes: more molecular partners than anticipated. , 2009, Biochimica et biophysica acta.

[11]  P. Farabaugh,et al.  The frequency of translational misreading errors in E. coli is largely determined by tRNA competition. , 2006, RNA.

[12]  I. Stansfield,et al.  The products of the SUP45 (eRF1) and SUP35 genes interact to mediate translation termination in Saccharomyces cerevisiae. , 1995, The EMBO journal.

[13]  V. Döring,et al.  Genetic Code Ambiguity , 2002, The Journal of Biological Chemistry.

[14]  T Suzuki,et al.  The 'polysemous' codon--a codon with multiple amino acid assignment caused by dual specificity of tRNA identity. , 1997, The EMBO journal.

[15]  H. True,et al.  A yeast prion provides a mechanism for genetic variation and phenotypic diversity , 2000, Nature.

[16]  D. Barford,et al.  The Crystal Structure of Human Eukaryotic Release Factor eRF1—Mechanism of Stop Codon Recognition and Peptidyl-tRNA Hydrolysis , 2000, Cell.

[17]  J. Masel,et al.  Complex Adaptations Can Drive the Evolution of the Capacitor [PSI +], Even with Realistic Rates of Yeast Sex , 2009, PLoS genetics.

[18]  M. Tuite,et al.  Translation termination efficiency can be regulated in Saccharomyces cerevisiae by environmental stress through a prion‐mediated mechanism , 1999, The EMBO journal.

[19]  Sergey V. Balashov,et al.  Escherichia coli Cells Bearing a Ribosomal Ambiguity Mutation in rpsD Have a Mutator Phenotype That Correlates with Increased Mistranslation , 2003, Journal of bacteriology.

[20]  M. Wilcox Gamma-glutamyl phosphate attached to glutamine-specific tRNA. A precursor of glutaminyl-tRNA in Bacillus subtilis. , 1969, European journal of biochemistry.

[21]  Shigeyuki Yokoyama,et al.  Structural insights into the second step of RNA-dependent cysteine biosynthesis in archaea: crystal structure of Sep-tRNA:Cys-tRNA synthase from Archaeoglobus fulgidus. , 2007, Journal of molecular biology.

[22]  Qian Wang,et al.  Expanding the genetic code for biological studies. , 2009, Chemistry & biology.

[23]  S. Rutherford,et al.  Between genotype and phenotype: protein chaperones and evolvability , 2003, Nature Reviews Genetics.

[24]  V. Ramakrishnan,et al.  First published online as a Review in Advance on February 25, 2005 STRUCTURAL INSIGHTS INTO TRANSLATIONAL , 2022 .

[25]  D. Söll,et al.  Pyrrolysine analogues as substrates for pyrrolysyl‐tRNA synthetase , 2006, FEBS letters.

[26]  S. Lindquist,et al.  Prion Switching in Response to Environmental Stress , 2008, PLoS biology.

[27]  P. Farabaugh,et al.  Translational Accuracy during Exponential, Postdiauxic, and Stationary Growth Phases in Saccharomyces cerevisiae , 2004, Eukaryotic Cell.

[28]  M. Tuite,et al.  The CUG codon is decoded in vivo as serine and not leucine in Candida albicans. , 1995, Nucleic acids research.

[29]  Manuel A. S. Santos,et al.  Evolution of pathogenicity and sexual reproduction in eight Candida genomes , 2009, Nature.

[30]  Shigeyuki Yokoyama,et al.  Structural insights into the first step of RNA-dependent cysteine biosynthesis in archaea , 2007, Nature Structural &Molecular Biology.

[31]  Ryohei Ishii,et al.  Multistep engineering of pyrrolysyl-tRNA synthetase to genetically encode N(epsilon)-(o-azidobenzyloxycarbonyl) lysine for site-specific protein modification. , 2008, Chemistry & biology.

[32]  J. Andreesen,et al.  Factors and Selenocysteine Insertion Sequence Requirements for the Synthesis of Selenoproteins from a Gram-Positive Anaerobe in Escherichia coli , 2007, Applied and Environmental Microbiology.

[33]  Dieter Söll,et al.  Natural expansion of the genetic code. , 2007, Nature chemical biology.

[34]  Dieter Söll,et al.  tRNA-dependent asparagine formation , 1996, Nature.

[35]  S. Yokoyama,et al.  Recognition of non-alpha-amino substrates by pyrrolysyl-tRNA synthetase. , 2009, Journal of molecular biology.

[36]  A. V. Lobanov,et al.  Genetic Code Supports Targeted Insertion of Two Amino Acids by One Codon , 2009, Science.

[37]  J. Ferry,et al.  Cysteine biosynthesis in the Archaea: Methanosarcina thermophila utilizes O-acetylserine sulfhydrylase. , 2000, FEMS microbiology letters.

[38]  M. Z. Humayun,et al.  DNA Polymerase III from Escherichia coliCells Expressing mutA Mistranslator tRNA Is Error-prone* , 2002, The Journal of Biological Chemistry.

[39]  M. Wilcox γ-Glutamyl Phosphate Attached to Glutamine-Specific tRNA , 1969 .

[40]  Paul Schimmel,et al.  Global effects of mistranslation from an editing defect in mammalian cells. , 2006, Chemistry & biology.

[41]  J. Parker,et al.  Missense misreading of asparagine codons as a function of codon identity and context. , 1987, The Journal of biological chemistry.

[42]  J. Ferry,et al.  O-Acetylserine Sulfhydrylase fromMethanosarcina thermophila , 2000, Journal of bacteriology.

[43]  D. Söll,et al.  Misacylation of pyrrolysine tRNA in vitro and in vivo , 2008, FEBS letters.

[44]  Manuel A. S. Santos,et al.  Critical roles for a genetic code alteration in the evolution of the genus Candida , 2007, The EMBO journal.

[45]  J. Sabina,et al.  Quality control despite mistranslation caused by an ambiguous genetic code , 2008, Proceedings of the National Academy of Sciences.

[46]  Gabriela R. Moura,et al.  A Genetic Code Alteration Is a Phenotype Diversity Generator in the Human Pathogen Candida albicans , 2007, PloS one.

[47]  Dieter Söll,et al.  From one amino acid to another: tRNA-dependent amino acid biosynthesis , 2008, Nucleic acids research.

[48]  M. Ibba,et al.  Aminoacyl-tRNA synthesis and translational quality control. , 2009, Annual review of microbiology.

[49]  D. Söll,et al.  Purification and functional characterization of glutamate-1-semialdehyde aminotransferase from Chlamydomonas reinhardtii. , 1991, The Journal of biological chemistry.

[50]  O. Namy,et al.  Epigenetic control of polyamines by the prion [PSI+] , 2008, Nature Cell Biology.

[51]  Yan Zhang,et al.  High content of proteins containing 21st and 22nd amino acids, selenocysteine and pyrrolysine, in a symbiotic deltaproteobacterium of gutless worm Olavius algarvensis , 2007, Nucleic acids research.