Structural insights into mRNA reading frame regulation by tRNA modification and slippery codon-anticodon pairing.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 33016876.
- Also identified by DOI 10.7554/eLife.51898 and PMC identifier 7577736.
- Licence recorded as CC BY.
- The licence permits redistribution, so the abstract is shown in full and the full text is available from the publisher.
Abstract
Modifications in the tRNA anticodon loop, adjacent to the three-nucleotide anticodon, influence translation fidelity by stabilizing the tRNA to allow for accurate reading of the mRNA genetic code. One example is the N1-methylguanosine modification at guanine nucleotide 37 (m<sup>1</sup>G37) located in the anticodon loop andimmediately adjacent to the anticodon nucleotides 34, 35, 36. The absence of m<sup>1</sup>G37 in tRNA<sup>Pro</sup> causes +1 frameshifting on polynucleotide, slippery codons. Here, we report structures of the bacterial ribosome containing tRNA<sup>Pro</sup> bound to either cognate or slippery codons to determine how the m<sup>1</sup>G37 modification prevents mRNA frameshifting. The structures reveal that certain codon-anticodon contexts and the lack of m<sup>1</sup>G37 destabilize interactions of tRNA<sup>Pro</sup> with the P site of the ribosome, causing large conformational changes typically only seen during EF-G-mediated translocation of the mRNA-tRNA pairs. These studies provide molecular insights into how m<sup>1</sup>G37 stabilizes the interactions of tRNA<sup>Pro</sup> with the ribosome in the context of a slippery mRNA codon.
Medical subject headings
- Anticodon
- Codon
- Escherichia coli
- Gene Expression Regulation, Bacterial
- RNA, Messenger
- Reading Frames