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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...
Autores principales: | , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2011
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Materias: | |
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 |
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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 |
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