Seven Amino Acid Types Suffice to Create the Core Fold of RNA Polymerase
Author(s) -
Sota Yagi,
Aditya K. Padhi,
Jelena Vučinić,
Sophie Barbe,
Thomas Schiex,
Reiko Nakagawa,
David Simoncini,
Kam Y. J. Zhang,
Shunsuke Tagami
Publication year - 2021
Publication title -
journal of the american chemical society
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 7.115
H-Index - 612
eISSN - 1520-5126
pISSN - 0002-7863
DOI - 10.1021/jacs.1c05367
Subject(s) - chemistry , genetic code , amino acid , polymerase , rna , gene , translation (biology) , biochemistry , computational biology , messenger rna , biology
The extant complex proteins must have evolved from ancient short and simple ancestors. The double-ψ β-barrel (DPBB) is one of the oldest protein folds and conserved in various fundamental enzymes, such as the core domain of RNA polymerase. Here, by reverse engineering a modern DPBB domain, we reconstructed its plausible evolutionary pathway started by "interlacing homodimerization" of a half-size peptide, followed by gene duplication and fusion. Furthermore, by simplifying the amino acid repertoire of the peptide, we successfully created the DPBB fold with only seven amino acid types (Ala, Asp, Glu, Gly, Lys, Arg, and Val), which can be coded by only GNN and ARR (R = A or G) codons in the modern translation system. Thus, the DPBB fold could have been materialized by the early translation system and genetic code.
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