Human tRNALYs3UUU Is Pre-Structured by Natural Modifications for Cognate and Wobble Codon Binding through Keto-Enol Tautomerism

JOURNAL OF MOLECULAR BIOLOGY

卷:416

Article

Vendeix, Franck A. P.²  Murphy, Frank V.³  Cantara, William A.^1,2  Leszczynska, Grazyna⁴  Gustilo, Estella M.²  Sproat, Brian⁵  Malkiewicz, Andrzej⁴  Agris, Paul F.^1,2 

[1] SUNY Albany, RNA Inst, Albany, NY 12222 USA

[2] N Carolina State Univ, Dept Mol & Struct Biochem, Raleigh, NC 27695 USA

[3] Argonne Natl Lab, NE Collaborat Access Team, Argonne, IL 60439 USA

[4] Tech Univ Lodz, Inst Organ Chem, PL-90924 Lodz, Poland

[5] Integrated DNA Technol BVBA, B-3000 Louvain, Belgium

关键词: modifications;    wobble decoding;    anticodon structure;    tRNA(LYs3);   

DOI  :  10.1016/j.jmb.2011.12.048

来源: Elsevier

【 摘 要 】

Human tRNA(UUU)(LYs3) (htRNA(UUU)(LYs3)) decodes the lysine codons AAA and AAG during translation and also plays a crucial role as the primer for HIV-1 (human immunodeficiency virus type 1) reverse transcription. The posttranscriptional modifications 5-methoxycarbonylmethy1-2-thiouridine (mcm(5)S(2)U(34)), 2-methylthio-N-6-threonylcarbamoyladenosine (ms(2)t(6)A(37)), and pseudouridirte (Psi(39)) in the tRNA's anticodon domain are critical for ribosomal binding and HIV-1 reverse transcription. To understand the importance of modified nucleoside contributions, we determined the structure and function of this tRNA's anticodon stem and loop (ASL) domain with these modifications at positions 34, 37, and 39, respectively (hASL(UUU)(Lys3)-mcm(5)s(2)U(34);ms(2)t(6)A(37);Psi(39)). Ribosome binding assays in vitro revealed that the hASL(UUU)(LYs3)-mcm(5)s(2)U(34);ms(2)t(6)A(37);Psi(39) bound AAA and AAG codons, whereas binding of the unmodified ASL(UUU)(LYs3) was barely detectable. The UV hyperchromicity, the circular dichroism, and the structural analyses indicated that Psi(39) enhanced the thermodynamic stability of the ASL through base stacking while ms(2)t(6)A(37) restrained the anticodon to adopt an open loop conformation that is required for ribosomal binding. The NMR-restrained molecular-dynamics-derived solution structure revealed that the modifications provided an open, ordered loop for codon binding. The crystal structures of the hASL(UUU)(LYs3)-mcm(5)s(2)U(34);ms(2)t(6)A(37);Psi(39) bound to the 30S ribosomal subunit with each codon in the A site showed that the modified nucleotides mcm(5)s(2)U(34) and ms(2)t(6)A(37) participate in the stability of the anticodon-codon interaction. Importantly, the mcm(5)s(2)U(34)center dot G3 wobble base pair is in the Watson-Crick geometry, requiring unusual hydrogen bonding to G in which mcm(5)s(2)U(34) must shift from the keto to the enol form. The results unambiguously demonstrate that modifications pre-structure the anticodon as a key prerequisite for efficient and accurate recognition of cognate and wobble codons. (C) 2011 Elsevier Ltd. All rights reserved.

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