Experimental solutions to problems defining the origin of codon-directed protein synthesis

Abstract

How genetic coding differentiated biology from chemistry is a long-standing challenge in Biology, for which there have been few experimental approaches, despite a wide-ranging speculative literature. We summarize five coordinated areas-experimental characterization of functional approximations to the minimal peptides (protozymes and urzymes) necessary to activate amino acids and acylate tRNA; showing that specificities of these experimental models match those expected from the synthetase Class division; population of disjoint regions of amino acid sequence space via bidirectional coding ancestry of the two synthetase Classes; showing that the phase transfer equilibria of amino acid side chains that form a two-dimensional basis set for protein folding are embedded in patterns of bases in the tRNA acceptor stem and anticodon; and identification of molecular signatures of ancestral synthetases and tRNAs necessary to define the earliest cognate synthetase:tRNA pairs-that now compose an extensive experimentally testable paradigm for progress toward understanding the coordinated emergence of the codon table and viable mRNA coding sequences. We briefly discuss recent progress toward identifying the remaining outstanding questions-the nature of the earliest amino acid alphabets and the origin of binding discrimination via distinct amino acid sequence-independent protein secondary structures-and how these, too, might be addressed experimentally.

Keywords: Aminoacyl-tRNA synthetase:tRNA cognate pairs; Bidirectional genetic coding; Protein folding; Self-organization of molecular recognition.