Evolution of the genetic code based on conservative changes of codons, amino acids, and aminoacyl tRNA synthetases

被引:18
|
作者
Rogers, Scott O. [1 ]
机构
[1] Bowling Green State Univ, Dept Biol Sci, Bowling Green, OH 43403 USA
关键词
Genetic code; Coevolution; Prebiotic Earth; Amino acid biochemistry; Phylogeny; Parsimony; ORIGIN; MODEL; COEVOLUTION; SEQUENCE; ANCIENT; PROTEIN;
D O I
10.1016/j.jtbi.2019.01.022
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
The genetic code, as arranged in the standard tabular form, displays a non-random structure relating to the characteristics of the amino acids. An alternative arrangement can be made by organizing the code according to aminoacyl-tRNA synthetases (aaRSs), codons, and reverse complement codons, which illuminates a coevolutionary process that led to the contemporary genetic code. As amino acids were added to the genetic code, they were recognized by aaRSs that interact with stereochemically similar amino acids. Single nucleotide changes in the codons and anticodons were favored over more extensive changes, such that there was a logical stepwise progression in the evolution of the genetic code. The model presented traces the evolution of the genetic code accounting for these steps. Amino acid frequencies in ancient proteins and the preponderance of GNN codons in mRNAs for ancient proteins indicate that the genetic code began with alanine, aspartate, glutamate, glycine, and valine, with alanine being in the highest proportions. In addition to being consistent in terms of conservative changes in codon nucleotides, the model also is consistent with respect to aaRS classes, aaRS attachment to the tRNA, amino acid stereochemistry, and to a large extent with amino acid physicochemistry, and biochemical pathways. (C) 2019 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1 / 10
页数:10
相关论文
共 50 条
  • [21] On the relative content of G,C bases in codons of amino acids corresponding to Class I and II aminoacyl-tRNA synthetases
    Cavalcanti, ARO
    Ferreira, R
    ORIGINS OF LIFE AND EVOLUTION OF BIOSPHERES, 2001, 31 (03): : 257 - 269
  • [22] INHIBITION OF AMINOACYL-TRNA SYNTHETASES BY ACYL DERIVATIVES OF AMINO-ACIDS
    ZEVINSONKIN, D
    HOCHBERG, AA
    FEBS LETTERS, 1974, 49 (01) : 125 - 128
  • [23] Characterization and directed evolution of aminoacyl tRNA synthetases
    Tullman, Jennifer
    Wu, Liming
    Li, Shuwei
    Marino, John
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2015, 249
  • [24] Evolution of structure in aminoacyl-tRNA synthetases
    O'Donoghue, P
    Luthey-Schulten, Z
    MICROBIOLOGY AND MOLECULAR BIOLOGY REVIEWS, 2003, 67 (04) : 550 - +
  • [25] Evolution of structure in the aminoacyl-tRNA synthetases
    O'Donoghue, PM
    Luthey-Schulten, Z
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2004, 227 : U275 - U275
  • [26] Structural Robustness Affects the Engineerability of Aminoacyl-tRNA Synthetases for Genetic Code Expansion
    Grasso, Katherine T.
    Yeo, Megan J. R.
    Hillenbrand, Christen M.
    Ficaretta, Elise D.
    Italia, James S.
    Huang, Rachel L.
    Chatterjee, Abhishek
    BIOCHEMISTRY, 2021, 60 (07) : 489 - 493
  • [27] Aminoacyl-tRNA synthetases and amino acid signaling
    Yu, Ya Chun
    Han, Jung Min
    Kim, Sunghoon
    BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH, 2021, 1868 (01):
  • [28] Origin of the genetic code: First aminoacyl-tRNA synthetases could replace isofunctional ribozymes when only the second base of codons was established
    Rodin, Sergei N.
    Rodin, Andrei S.
    DNA AND CELL BIOLOGY, 2006, 25 (06) : 365 - 375
  • [29] Aminoacyl-tRNA synthetase evolution and sectoring of the genetic code
    Pak, Daewoo
    Kim, Yunsoo
    Burton, Zachary F.
    TRANSCRIPTION-AUSTIN, 2018, 9 (04): : 205 - 224
  • [30] Engineered Aminoacyl-tRNA Synthetases with Improved Selectivity toward Noncanonical Amino Acids
    Kwok, Hui Si
    Vargas-Rodriguez, Oscar
    Melnikov, Sergey V.
    Soll, Dieter
    ACS CHEMICAL BIOLOGY, 2019, 14 (04) : 603 - 612