Cargando…

Evidence for an RNA pseudoknot loop-helix interaction essential for efficient −1 ribosomal frameshifting

RNA pseudoknots are structural elements that participate in a variety of biological processes. At −1 ribosomal frameshifting sites, several types of pseudoknot have been identified which differ in their organisation and functionality. The pseudoknot found in infectious bronchitis virus (IBV) is typi...

Descripción completa

Detalles Bibliográficos
Autores principales: Liphardt, Jan, Napthine, Sawsan, Kontos, Harry, Brierley, Ian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Academic Press. 1999
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7141562/
https://www.ncbi.nlm.nih.gov/pubmed/10329145
http://dx.doi.org/10.1006/jmbi.1999.2689
_version_ 1783519219215761408
author Liphardt, Jan
Napthine, Sawsan
Kontos, Harry
Brierley, Ian
author_facet Liphardt, Jan
Napthine, Sawsan
Kontos, Harry
Brierley, Ian
author_sort Liphardt, Jan
collection PubMed
description RNA pseudoknots are structural elements that participate in a variety of biological processes. At −1 ribosomal frameshifting sites, several types of pseudoknot have been identified which differ in their organisation and functionality. The pseudoknot found in infectious bronchitis virus (IBV) is typical of those that possess a long stem 1 of 11-12 bp and a long loop 2 (30-164 nt). A second group of pseudoknots are distinguishable that contain stems of only 5 to 7 bp and shorter loops. The NMR structure of one such pseudoknot, that of mouse mammary tumor virus (MMTV), has revealed that it is kinked at the stem 1-stem 2 junction, and that this kinked conformation is essential for efficient frameshifting. We recently investigated the effect on frameshifting of modulating stem 1 length and stability in IBV-based pseudoknots, and found that a stem 1 with at least 11 bp was needed for efficient frameshifting. Here, we describe the sequence manipulations that are necessary to bypass the requirement for an 11 bp stem 1 and to convert a short non-functional IBV-derived pseudoknot into a highly efficient, kinked frameshifter pseudoknot. Simple insertion of an adenine residue at the stem 1-stem 2 junction (an essential feature of a kinked pseudoknot) was not sufficient to create a functional pseudoknot. An additional change was needed: efficient frameshifting was recovered only when the last nucleotide of loop 2 was changed from a G to an A. The requirement for an A at the end of loop 2 is consistent with a loop-helix contact similar to those described in other RNA tertiary structures. A mutational analysis of both partners of the proposed interaction, the loop 2 terminal adenine residue and two G·C pairs near the top of stem 1, revealed that the interaction was essential for efficient frameshifting. The specific requirement for a 3′-terminal A residue was lost when loop 2 was increased from 8 to 14 nt, suggesting that the loop-helix contact may be required only in those pseudoknots with a short loop 2.
format Online
Article
Text
id pubmed-7141562
institution National Center for Biotechnology Information
language English
publishDate 1999
publisher Academic Press.
record_format MEDLINE/PubMed
spelling pubmed-71415622020-04-09 Evidence for an RNA pseudoknot loop-helix interaction essential for efficient −1 ribosomal frameshifting Liphardt, Jan Napthine, Sawsan Kontos, Harry Brierley, Ian J Mol Biol Article RNA pseudoknots are structural elements that participate in a variety of biological processes. At −1 ribosomal frameshifting sites, several types of pseudoknot have been identified which differ in their organisation and functionality. The pseudoknot found in infectious bronchitis virus (IBV) is typical of those that possess a long stem 1 of 11-12 bp and a long loop 2 (30-164 nt). A second group of pseudoknots are distinguishable that contain stems of only 5 to 7 bp and shorter loops. The NMR structure of one such pseudoknot, that of mouse mammary tumor virus (MMTV), has revealed that it is kinked at the stem 1-stem 2 junction, and that this kinked conformation is essential for efficient frameshifting. We recently investigated the effect on frameshifting of modulating stem 1 length and stability in IBV-based pseudoknots, and found that a stem 1 with at least 11 bp was needed for efficient frameshifting. Here, we describe the sequence manipulations that are necessary to bypass the requirement for an 11 bp stem 1 and to convert a short non-functional IBV-derived pseudoknot into a highly efficient, kinked frameshifter pseudoknot. Simple insertion of an adenine residue at the stem 1-stem 2 junction (an essential feature of a kinked pseudoknot) was not sufficient to create a functional pseudoknot. An additional change was needed: efficient frameshifting was recovered only when the last nucleotide of loop 2 was changed from a G to an A. The requirement for an A at the end of loop 2 is consistent with a loop-helix contact similar to those described in other RNA tertiary structures. A mutational analysis of both partners of the proposed interaction, the loop 2 terminal adenine residue and two G·C pairs near the top of stem 1, revealed that the interaction was essential for efficient frameshifting. The specific requirement for a 3′-terminal A residue was lost when loop 2 was increased from 8 to 14 nt, suggesting that the loop-helix contact may be required only in those pseudoknots with a short loop 2. Academic Press. 1999-05-07 2002-05-25 /pmc/articles/PMC7141562/ /pubmed/10329145 http://dx.doi.org/10.1006/jmbi.1999.2689 Text en Copyright © 1999 Academic Press. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Article
Liphardt, Jan
Napthine, Sawsan
Kontos, Harry
Brierley, Ian
Evidence for an RNA pseudoknot loop-helix interaction essential for efficient −1 ribosomal frameshifting
title Evidence for an RNA pseudoknot loop-helix interaction essential for efficient −1 ribosomal frameshifting
title_full Evidence for an RNA pseudoknot loop-helix interaction essential for efficient −1 ribosomal frameshifting
title_fullStr Evidence for an RNA pseudoknot loop-helix interaction essential for efficient −1 ribosomal frameshifting
title_full_unstemmed Evidence for an RNA pseudoknot loop-helix interaction essential for efficient −1 ribosomal frameshifting
title_short Evidence for an RNA pseudoknot loop-helix interaction essential for efficient −1 ribosomal frameshifting
title_sort evidence for an rna pseudoknot loop-helix interaction essential for efficient −1 ribosomal frameshifting
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7141562/
https://www.ncbi.nlm.nih.gov/pubmed/10329145
http://dx.doi.org/10.1006/jmbi.1999.2689
work_keys_str_mv AT liphardtjan evidenceforanrnapseudoknotloophelixinteractionessentialforefficient1ribosomalframeshifting
AT napthinesawsan evidenceforanrnapseudoknotloophelixinteractionessentialforefficient1ribosomalframeshifting
AT kontosharry evidenceforanrnapseudoknotloophelixinteractionessentialforefficient1ribosomalframeshifting
AT brierleyian evidenceforanrnapseudoknotloophelixinteractionessentialforefficient1ribosomalframeshifting