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Unusual base pairing during the decoding of a stop codon by the ribosome

During normal translation, binding of a release factor to one of the three stop codons (UGA, UAA or UAG) results in termination of protein synthesis. However, modification of the initial uridine to a pseudouridine (Ψ) allows efficient recognition and read-through of these stop codons by a transfer R...

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Autores principales: Fernández, Israel S., Ng, Chyan Leong, Kelley, Ann C., Wu, Guowei, Yu, Yi-Tao, Ramakrishnan, V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3732562/
https://www.ncbi.nlm.nih.gov/pubmed/23812587
http://dx.doi.org/10.1038/nature12302
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author Fernández, Israel S.
Ng, Chyan Leong
Kelley, Ann C.
Wu, Guowei
Yu, Yi-Tao
Ramakrishnan, V.
author_facet Fernández, Israel S.
Ng, Chyan Leong
Kelley, Ann C.
Wu, Guowei
Yu, Yi-Tao
Ramakrishnan, V.
author_sort Fernández, Israel S.
collection PubMed
description During normal translation, binding of a release factor to one of the three stop codons (UGA, UAA or UAG) results in termination of protein synthesis. However, modification of the initial uridine to a pseudouridine (Ψ) allows efficient recognition and read-through of these stop codons by a transfer RNA (tRNA), although it requires formation of two normally forbidden purine-purine base pairs(1). We have determined the crystal structure at 3.1 Å resolution of the 30S ribosomal subunit in complex with the anticodon stem loop of tRNA(Ser) bound to the ΨAG stop codon in the A site. The ΨA base pair at the first position is accompanied by the formation of purine-purine base pairs at the second and third positions of the codon, which display an unusual Watson-Crick/Hoogsteen geometry. The structure shows a previously unsuspected ability of the ribosomal decoding center to accommodate non-canonical base pairs.
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spelling pubmed-37325622014-02-01 Unusual base pairing during the decoding of a stop codon by the ribosome Fernández, Israel S. Ng, Chyan Leong Kelley, Ann C. Wu, Guowei Yu, Yi-Tao Ramakrishnan, V. Nature Article During normal translation, binding of a release factor to one of the three stop codons (UGA, UAA or UAG) results in termination of protein synthesis. However, modification of the initial uridine to a pseudouridine (Ψ) allows efficient recognition and read-through of these stop codons by a transfer RNA (tRNA), although it requires formation of two normally forbidden purine-purine base pairs(1). We have determined the crystal structure at 3.1 Å resolution of the 30S ribosomal subunit in complex with the anticodon stem loop of tRNA(Ser) bound to the ΨAG stop codon in the A site. The ΨA base pair at the first position is accompanied by the formation of purine-purine base pairs at the second and third positions of the codon, which display an unusual Watson-Crick/Hoogsteen geometry. The structure shows a previously unsuspected ability of the ribosomal decoding center to accommodate non-canonical base pairs. 2013-06-30 2013-08-01 /pmc/articles/PMC3732562/ /pubmed/23812587 http://dx.doi.org/10.1038/nature12302 Text en Users may view, print, copy, download and text and data- mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use: http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
Fernández, Israel S.
Ng, Chyan Leong
Kelley, Ann C.
Wu, Guowei
Yu, Yi-Tao
Ramakrishnan, V.
Unusual base pairing during the decoding of a stop codon by the ribosome
title Unusual base pairing during the decoding of a stop codon by the ribosome
title_full Unusual base pairing during the decoding of a stop codon by the ribosome
title_fullStr Unusual base pairing during the decoding of a stop codon by the ribosome
title_full_unstemmed Unusual base pairing during the decoding of a stop codon by the ribosome
title_short Unusual base pairing during the decoding of a stop codon by the ribosome
title_sort unusual base pairing during the decoding of a stop codon by the ribosome
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3732562/
https://www.ncbi.nlm.nih.gov/pubmed/23812587
http://dx.doi.org/10.1038/nature12302
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