4.3 Article

RNA affinity for molecular L-histidine; Genetic code origins

Journal

JOURNAL OF MOLECULAR EVOLUTION
Volume 61, Issue 2, Pages 226-235

Publisher

SPRINGER
DOI: 10.1007/s00239-004-0360-9

Keywords

selection; SELEX; amino acid; coding; triplet

Funding

  1. NIGMS NIH HHS [GM 48080] Funding Source: Medline

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Selection for affinity for free histidine yields a single RNA aptamer, which was isolated 54 times independently. This RNA is highly specific for the side chain and binds protonated L-histidine with 10(2)-10(3)-fold stereoselectivity and a dissociation constant (K-D) of 8-54 mu M in different isolates. These histidine-binding RNAs have a common internal loop-hairpin loop structure, based on a conserved RAAGUGGGKKN(0-36) AUGUN(0-2)AGKAACAG sequence. Notably, the repetitively isolated sequence contains two histidine anticodons, both implicated by conservation and chemical data in amino acid affinity. This site is probably the simplest structure that can meet our histidine affinity selection, which strengthens experimental support for a stereochemical origin of the genetic code.

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