Evolution of the Standard Genetic Code

被引:0
作者
Michael Yarus
机构
[1] University of Colorado Boulder,Department of Molecular, Cellular and Developmental Biology
来源
Journal of Molecular Evolution | 2021年 / 89卷
关键词
Coding table; Codon; Triplet; Evolution; Distribution fitness;
D O I
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中图分类号
学科分类号
摘要
A near-universal Standard Genetic Code (SGC) implies a single origin for present Earth life. To study this unique event, I compute paths to the SGC, comparing different plausible histories. Notably, SGC-like coding emerges from traditional evolutionary mechanisms, and a superior route can be identified. To objectively measure evolution, progress values from 0 (random coding) to 1 (SGC-like) are defined: these measure fractions of random-code-to-SGC distance. Progress types are spacing/distance/delta Polar Requirement, detecting space between identical assignments/mutational distance to the SGC/chemical order, respectively. The coding system is based on selected RNAs performing aminoacyl-RNA synthetase reactions. Acceptor RNAs exhibit SGC-like Crick wobble; alternatively, non-wobbling triplets uniquely encode 20 amino acids/start/stop. Triplets acquire 22 functions by stereochemistry, selection, coevolution, or at random. Assignments also propagate to an assigned triplet’s neighborhood via single mutations, but can also decay. A vast code universe makes futile evolutionary paths plentiful. Thus, SGC evolution is critically sensitive to disorder from random assignments. Evolution also inevitably slows near coding completion. The SGC likely avoided these difficulties, and two suitable paths are compared. In late wobble, a majority of non-wobble assignments are made before wobble is adopted. In continuous wobble, a uniquely advantageous early intermediate yields an ordered SGC. Revised coding evolution (limited randomness, late wobble, concentration on amino acid encoding, chemically conservative coevolution with a chemically ordered elite) produces varied full codes with excellent joint progress values. A population of only 600 independent coding tables includes SGC-like members; a Bayesian path toward more accurate SGC evolution is available.
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页码:19 / 44
页数:25
相关论文
共 137 条
[1]  
Adio S(2018)Dynamics of ribosomes and release factors during translation termination in eLife 7 e34252-476
[2]  
Sharma H(1997). J Mol Evol 44 473-799
[3]  
Senyushkina T(2014)An analysis of the metabolic theory of the origin of the genetic code Life Basel Switz 4 788-347
[4]  
Karki P(2017)On the contribution of protein spatial organization to the physicochemical interconnection between proteins and their cognate mRNAs Biochemistry 56 345-184
[5]  
Maracci C(2013)The biology of free guanidine as revealed by riboswitches J Mol Evol 77 170-24
[6]  
Wohlgemuth I(2019)A realistic model under which the genetic code is optimal Int J Mol Sci 20 1-5263
[7]  
Holtkamp W(2009)The origin and evolution of release factors: implications for translation termination, ribosome rescue, and quality control pathways J Am Chem Soc 131 5257-555
[8]  
Peske F(1966)Rapid and simple ribozymic aminoacylation using three conserved nucleotides J Mol Biol 19 548-379
[9]  
Rodnina MV(1968)Codon–anticodon pairing: the wobble hypothesis J Mol Biol 38 367-622
[10]  
Amirnovin R(2002)The origin of the genetic code J Mol Evol 55 616-9