Cargando…

Endogenous ribosomal frameshift signals operate as mRNA destabilizing elements through at least two molecular pathways in yeast

Although first discovered in viruses, previous studies have identified operational −1 ribosomal frameshifting (−1 RF) signals in eukaryotic genomic sequences, and suggested a role in mRNA stability. Here, four yeast −1 RF signals are shown to promote significant mRNA destabilization through the nons...

Descripción completa

Detalles Bibliográficos
Autores principales: Belew, Ashton T., Advani, Vivek M., Dinman, Jonathan D.
Formato: Texto
Lenguaje:English
Publicado: Oxford University Press 2011
Materias:
RNA
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3074144/
https://www.ncbi.nlm.nih.gov/pubmed/21109528
http://dx.doi.org/10.1093/nar/gkq1220
_version_ 1782201694279434240
author Belew, Ashton T.
Advani, Vivek M.
Dinman, Jonathan D.
author_facet Belew, Ashton T.
Advani, Vivek M.
Dinman, Jonathan D.
author_sort Belew, Ashton T.
collection PubMed
description Although first discovered in viruses, previous studies have identified operational −1 ribosomal frameshifting (−1 RF) signals in eukaryotic genomic sequences, and suggested a role in mRNA stability. Here, four yeast −1 RF signals are shown to promote significant mRNA destabilization through the nonsense mediated mRNA decay pathway (NMD), and genetic evidence is presented suggesting that they may also operate through the no-go decay pathway (NGD) as well. Yeast EST2 mRNA is highly unstable and contains up to five −1 RF signals. Ablation of the −1 RF signals or of NMD stabilizes this mRNA, and changes in −1 RF efficiency have opposing effects on the steady-state abundance of the EST2 mRNA. These results demonstrate that endogenous −1 RF signals function as mRNA destabilizing elements through at least two molecular pathways in yeast. Consistent with current evolutionary theory, phylogenetic analyses suggest that −1 RF signals are rapidly evolving cis-acting regulatory elements. Identification of high confidence −1 RF signals in ∼10% of genes in all eukaryotic genomes surveyed suggests that −1 RF is a broadly used post-transcriptional regulator of gene expression.
format Text
id pubmed-3074144
institution National Center for Biotechnology Information
language English
publishDate 2011
publisher Oxford University Press
record_format MEDLINE/PubMed
spelling pubmed-30741442011-04-12 Endogenous ribosomal frameshift signals operate as mRNA destabilizing elements through at least two molecular pathways in yeast Belew, Ashton T. Advani, Vivek M. Dinman, Jonathan D. Nucleic Acids Res RNA Although first discovered in viruses, previous studies have identified operational −1 ribosomal frameshifting (−1 RF) signals in eukaryotic genomic sequences, and suggested a role in mRNA stability. Here, four yeast −1 RF signals are shown to promote significant mRNA destabilization through the nonsense mediated mRNA decay pathway (NMD), and genetic evidence is presented suggesting that they may also operate through the no-go decay pathway (NGD) as well. Yeast EST2 mRNA is highly unstable and contains up to five −1 RF signals. Ablation of the −1 RF signals or of NMD stabilizes this mRNA, and changes in −1 RF efficiency have opposing effects on the steady-state abundance of the EST2 mRNA. These results demonstrate that endogenous −1 RF signals function as mRNA destabilizing elements through at least two molecular pathways in yeast. Consistent with current evolutionary theory, phylogenetic analyses suggest that −1 RF signals are rapidly evolving cis-acting regulatory elements. Identification of high confidence −1 RF signals in ∼10% of genes in all eukaryotic genomes surveyed suggests that −1 RF is a broadly used post-transcriptional regulator of gene expression. Oxford University Press 2011-04 2010-11-24 /pmc/articles/PMC3074144/ /pubmed/21109528 http://dx.doi.org/10.1093/nar/gkq1220 Text en © The Author(s) 2010. Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/2.5 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.5), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle RNA
Belew, Ashton T.
Advani, Vivek M.
Dinman, Jonathan D.
Endogenous ribosomal frameshift signals operate as mRNA destabilizing elements through at least two molecular pathways in yeast
title Endogenous ribosomal frameshift signals operate as mRNA destabilizing elements through at least two molecular pathways in yeast
title_full Endogenous ribosomal frameshift signals operate as mRNA destabilizing elements through at least two molecular pathways in yeast
title_fullStr Endogenous ribosomal frameshift signals operate as mRNA destabilizing elements through at least two molecular pathways in yeast
title_full_unstemmed Endogenous ribosomal frameshift signals operate as mRNA destabilizing elements through at least two molecular pathways in yeast
title_short Endogenous ribosomal frameshift signals operate as mRNA destabilizing elements through at least two molecular pathways in yeast
title_sort endogenous ribosomal frameshift signals operate as mrna destabilizing elements through at least two molecular pathways in yeast
topic RNA
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3074144/
https://www.ncbi.nlm.nih.gov/pubmed/21109528
http://dx.doi.org/10.1093/nar/gkq1220
work_keys_str_mv AT belewashtont endogenousribosomalframeshiftsignalsoperateasmrnadestabilizingelementsthroughatleasttwomolecularpathwaysinyeast
AT advanivivekm endogenousribosomalframeshiftsignalsoperateasmrnadestabilizingelementsthroughatleasttwomolecularpathwaysinyeast
AT dinmanjonathand endogenousribosomalframeshiftsignalsoperateasmrnadestabilizingelementsthroughatleasttwomolecularpathwaysinyeast