Literature DB >> 31120344

Bias for 3'-Dominant Codon Directional Asymmetry in Theoretical Minimal RNA Rings.

Jacques Demongeot1, Hervé Seligmann2.   

Abstract

Aminoacyl tRNA synthetases ligate tRNAs specifically with their cognate amino acid. These synthetases are among life's earliest proteins, class II tRNA synthetases (cognates A, D, F, G, H, K, N, P, S, and T) presumably preceding class I tRNA synthetases (cognates C, E, I, L, M, Q, R, V, W, and Y). Classification of codons into palindromic (structure XYX), 5'-dominant (YXX), and 3'-dominant (XXY) (Codon Directional Asymmetry [CDA]) shows that class II tRNA synthetases aminoacylate amino acids associated with XXY. Our working hypothesis expects bias for XXY codons in primordial RNAs, such as theoretical minimal RNA rings, designed in silico to mimic life's earliest RNAs. Twenty-five RNA rings have been computed, which code over a minimal length (22 nucleotides) for a start codon, stop codon, and one and only one codon for each of the 20 amino acids, and form stem-loop hairpins preventing degradation; these 25 minimal RNAs are the only ones matching these constraints and they seem homologous to consensus tRNA sequences. This similarity defined candidate RNA ring anticodons and corresponding cognate amino acids. Here, analyses of RNA ring codon contents confirm bias for XXY codons in 13 among 14 RNA rings with unequal XXY and YXX codon numbers. This bias increases with the genetic code integration order of the RNA ring's cognate amino acid across and within tRNA synthetase classes, suggesting that evolutionary processes, and not physicochemical constraints, produced the association between CDA and tRNA synthetase classes. The self-referential hypothesis for genetic code origin, a very complete genetic code evolutionary hypothesis integrating many translational machinery components, predicts best among genetic code evolutionary hypotheses CDA biases in RNA rings. The RNA rings' simple design inadvertently reproduces CDAs predicted by the genetic code's structure, confirming theoretical minimal RNA rings as good proxies for life's earliest RNAs.

Entities:  

Keywords:  anticodon loop; cloverleaf secondary structure; comma-free codes; tRNA synthetase class

Year:  2019        PMID: 31120344     DOI: 10.1089/cmb.2018.0256

Source DB:  PubMed          Journal:  J Comput Biol        ISSN: 1066-5277            Impact factor:   1.479


  5 in total

1.  Pentamers with Non-redundant Frames: Bias for Natural Circular Code Codons.

Authors:  Jacques Demongeot; Hervé Seligmann
Journal:  J Mol Evol       Date:  2020-01-07       Impact factor: 2.395

2.  Footprints of a Singular 22-Nucleotide RNA Ring at the Origin of Life.

Authors:  Jacques Demongeot; Alexandra Henrion-Caude
Journal:  Biology (Basel)       Date:  2020-04-25

3.  Comparisons between small ribosomal RNA and theoretical minimal RNA ring secondary structures confirm phylogenetic and structural accretion histories.

Authors:  Jacques Demongeot; Hervé Seligmann
Journal:  Sci Rep       Date:  2020-05-06       Impact factor: 4.379

4.  Codon Directional Asymmetry Suggests Swapped Prebiotic 1st and 2nd Codon Positions.

Authors:  Hervé Seligmann; Jacques Demongeot
Journal:  Int J Mol Sci       Date:  2020-01-05       Impact factor: 5.923

5.  The primordial tRNA acceptor stem code from theoretical minimal RNA ring clusters.

Authors:  Jacques Demongeot; Hervé Seligmann
Journal:  BMC Genet       Date:  2020-01-23       Impact factor: 2.797

  5 in total

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