Abstract
AbstractA 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.
Publisher
Springer Science and Business Media LLC
Subject
Genetics,Molecular Biology,Ecology, Evolution, Behavior and Systematics
Reference57 articles.
1. Adio S, Sharma H, Senyushkina T, Karki P, Maracci C, Wohlgemuth I, Holtkamp W, Peske F, Rodnina MV (2018) Dynamics of ribosomes and release factors during translation termination in E. coli. eLife 7:e34252. https://doi.org/10.7554/eLife.34252
2. Amirnovin R (1997) An analysis of the metabolic theory of the origin of the genetic code. J Mol Evol 44:473–476
3. Beier A, Zagrovic B, Polyansky AA (2014) On the contribution of protein spatial organization to the physicochemical interconnection between proteins and their cognate mRNAs. Life Basel Switz 4:788–799
4. Breaker RR, Atilho RM, Malkowski SN, Nelson JW, Sherlock ME (2017) The biology of free guanidine as revealed by riboswitches. Biochemistry 56:345–347
5. Buhrman H, van der Gulik PTS, Klau GW, Schaffner C, Speijer D, Stougie L (2013) A realistic model under which the genetic code is optimal. J Mol Evol 77:170–184
Cited by
18 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献