Cargando…

New scoring system to identify RNA G-quadruplex folding

G-quadruplexes (G4s) are non-canonical structures involved in many important cellular processes. To date, the prediction of potential G-quadruplex structures (PG4s) has been based almost exclusively on the sequence of interest agreeing with the algorithm G(x)-N-(1–7)-G(x)-N(1–7)-G(x)-N(1–7)-G(x) (wh...

Descripción completa

Detalles Bibliográficos
Autores principales: Beaudoin, Jean-Denis, Jodoin, Rachel, Perreault, Jean-Pierre
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2014
Materias:
RNA
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3902908/
https://www.ncbi.nlm.nih.gov/pubmed/24121682
http://dx.doi.org/10.1093/nar/gkt904
_version_ 1782301042368577536
author Beaudoin, Jean-Denis
Jodoin, Rachel
Perreault, Jean-Pierre
author_facet Beaudoin, Jean-Denis
Jodoin, Rachel
Perreault, Jean-Pierre
author_sort Beaudoin, Jean-Denis
collection PubMed
description G-quadruplexes (G4s) are non-canonical structures involved in many important cellular processes. To date, the prediction of potential G-quadruplex structures (PG4s) has been based almost exclusively on the sequence of interest agreeing with the algorithm G(x)-N-(1–7)-G(x)-N(1–7)-G(x)-N(1–7)-G(x) (where x ≥ 3 and N = A, U, G or C). However, many sequences agreeing with this algorithm do not form G4s and are considered false-positive predictions. Here we show the RNA PG4 candidate in the 3′-untranslated region (UTR) of the TTYH1 gene to be one such false positive. Specifically, G4 folding was observed to be inhibited by the presence of multiple-cytosine tracks, located in the candidate’s genomic context, that adopted a Watson–Crick base-paired structure. Clearly, the neighbouring sequences of a PG4 may influence its folding. The secondary structure of 12 PG4 motifs along with either 15 or 50 nucleotides of their upstream and downstream genomic contexts were evaluated by in-line probing. Data permitted the development of a scoring system for the prediction of PG4s taking into account the effect of the neighbouring sequences. The accuracy of this scoring system was assessed by probing 14 other novel PG4 candidates retrieved in human 5′-UTRs. This new scoring system can be used, in combination with the standard algorithm, to better predict the folding of RNA G4s.
format Online
Article
Text
id pubmed-3902908
institution National Center for Biotechnology Information
language English
publishDate 2014
publisher Oxford University Press
record_format MEDLINE/PubMed
spelling pubmed-39029082014-01-27 New scoring system to identify RNA G-quadruplex folding Beaudoin, Jean-Denis Jodoin, Rachel Perreault, Jean-Pierre Nucleic Acids Res RNA G-quadruplexes (G4s) are non-canonical structures involved in many important cellular processes. To date, the prediction of potential G-quadruplex structures (PG4s) has been based almost exclusively on the sequence of interest agreeing with the algorithm G(x)-N-(1–7)-G(x)-N(1–7)-G(x)-N(1–7)-G(x) (where x ≥ 3 and N = A, U, G or C). However, many sequences agreeing with this algorithm do not form G4s and are considered false-positive predictions. Here we show the RNA PG4 candidate in the 3′-untranslated region (UTR) of the TTYH1 gene to be one such false positive. Specifically, G4 folding was observed to be inhibited by the presence of multiple-cytosine tracks, located in the candidate’s genomic context, that adopted a Watson–Crick base-paired structure. Clearly, the neighbouring sequences of a PG4 may influence its folding. The secondary structure of 12 PG4 motifs along with either 15 or 50 nucleotides of their upstream and downstream genomic contexts were evaluated by in-line probing. Data permitted the development of a scoring system for the prediction of PG4s taking into account the effect of the neighbouring sequences. The accuracy of this scoring system was assessed by probing 14 other novel PG4 candidates retrieved in human 5′-UTRs. This new scoring system can be used, in combination with the standard algorithm, to better predict the folding of RNA G4s. Oxford University Press 2014-01 2013-10-08 /pmc/articles/PMC3902908/ /pubmed/24121682 http://dx.doi.org/10.1093/nar/gkt904 Text en © The Author(s) 2013. Published by Oxford University Press. http://creativecommons.org/licenses/by/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle RNA
Beaudoin, Jean-Denis
Jodoin, Rachel
Perreault, Jean-Pierre
New scoring system to identify RNA G-quadruplex folding
title New scoring system to identify RNA G-quadruplex folding
title_full New scoring system to identify RNA G-quadruplex folding
title_fullStr New scoring system to identify RNA G-quadruplex folding
title_full_unstemmed New scoring system to identify RNA G-quadruplex folding
title_short New scoring system to identify RNA G-quadruplex folding
title_sort new scoring system to identify rna g-quadruplex folding
topic RNA
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3902908/
https://www.ncbi.nlm.nih.gov/pubmed/24121682
http://dx.doi.org/10.1093/nar/gkt904
work_keys_str_mv AT beaudoinjeandenis newscoringsystemtoidentifyrnagquadruplexfolding
AT jodoinrachel newscoringsystemtoidentifyrnagquadruplexfolding
AT perreaultjeanpierre newscoringsystemtoidentifyrnagquadruplexfolding