Cargando…
Deciphering the rules by which dynamics of mRNA secondary structure affect translation efficiency in Saccharomyces cerevisiae
Messenger RNA (mRNA) secondary structure decreases the elongation rate, as ribosomes must unwind every structure they encounter during translation. Therefore, the strength of mRNA secondary structure is assumed to be reduced in highly translated mRNAs. However, previous studies in vitro reported a p...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2014
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4005662/ https://www.ncbi.nlm.nih.gov/pubmed/24561808 http://dx.doi.org/10.1093/nar/gku159 |
_version_ | 1782314136283119616 |
---|---|
author | Mao, Yuanhui Liu, HuiLing Liu, Yanlin Tao, Shiheng |
author_facet | Mao, Yuanhui Liu, HuiLing Liu, Yanlin Tao, Shiheng |
author_sort | Mao, Yuanhui |
collection | PubMed |
description | Messenger RNA (mRNA) secondary structure decreases the elongation rate, as ribosomes must unwind every structure they encounter during translation. Therefore, the strength of mRNA secondary structure is assumed to be reduced in highly translated mRNAs. However, previous studies in vitro reported a positive correlation between mRNA folding strength and protein abundance. The counterintuitive finding suggests that mRNA secondary structure affects translation efficiency in an undetermined manner. Here, we analyzed the folding behavior of mRNA during translation and its effect on translation efficiency. We simulated translation process based on a novel computational model, taking into account the interactions among ribosomes, codon usage and mRNA secondary structures. We showed that mRNA secondary structure shortens ribosomal distance through the dynamics of folding strength. Notably, when adjacent ribosomes are close, mRNA secondary structures between them disappear, and codon usage determines the elongation rate. More importantly, our results showed that the combined effect of mRNA secondary structure and codon usage in highly translated mRNAs causes a short ribosomal distance in structural regions, which in turn eliminates the structures during translation, leading to a high elongation rate. Together, these findings reveal how the dynamics of mRNA secondary structure coupling with codon usage affect translation efficiency. |
format | Online Article Text |
id | pubmed-4005662 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-40056622014-05-01 Deciphering the rules by which dynamics of mRNA secondary structure affect translation efficiency in Saccharomyces cerevisiae Mao, Yuanhui Liu, HuiLing Liu, Yanlin Tao, Shiheng Nucleic Acids Res Computational Biology Messenger RNA (mRNA) secondary structure decreases the elongation rate, as ribosomes must unwind every structure they encounter during translation. Therefore, the strength of mRNA secondary structure is assumed to be reduced in highly translated mRNAs. However, previous studies in vitro reported a positive correlation between mRNA folding strength and protein abundance. The counterintuitive finding suggests that mRNA secondary structure affects translation efficiency in an undetermined manner. Here, we analyzed the folding behavior of mRNA during translation and its effect on translation efficiency. We simulated translation process based on a novel computational model, taking into account the interactions among ribosomes, codon usage and mRNA secondary structures. We showed that mRNA secondary structure shortens ribosomal distance through the dynamics of folding strength. Notably, when adjacent ribosomes are close, mRNA secondary structures between them disappear, and codon usage determines the elongation rate. More importantly, our results showed that the combined effect of mRNA secondary structure and codon usage in highly translated mRNAs causes a short ribosomal distance in structural regions, which in turn eliminates the structures during translation, leading to a high elongation rate. Together, these findings reveal how the dynamics of mRNA secondary structure coupling with codon usage affect translation efficiency. Oxford University Press 2014-04 2014-02-21 /pmc/articles/PMC4005662/ /pubmed/24561808 http://dx.doi.org/10.1093/nar/gku159 Text en © Crown copyright 2014. |
spellingShingle | Computational Biology Mao, Yuanhui Liu, HuiLing Liu, Yanlin Tao, Shiheng Deciphering the rules by which dynamics of mRNA secondary structure affect translation efficiency in Saccharomyces cerevisiae |
title | Deciphering the rules by which dynamics of mRNA secondary structure affect translation efficiency in Saccharomyces cerevisiae |
title_full | Deciphering the rules by which dynamics of mRNA secondary structure affect translation efficiency in Saccharomyces cerevisiae |
title_fullStr | Deciphering the rules by which dynamics of mRNA secondary structure affect translation efficiency in Saccharomyces cerevisiae |
title_full_unstemmed | Deciphering the rules by which dynamics of mRNA secondary structure affect translation efficiency in Saccharomyces cerevisiae |
title_short | Deciphering the rules by which dynamics of mRNA secondary structure affect translation efficiency in Saccharomyces cerevisiae |
title_sort | deciphering the rules by which dynamics of mrna secondary structure affect translation efficiency in saccharomyces cerevisiae |
topic | Computational Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4005662/ https://www.ncbi.nlm.nih.gov/pubmed/24561808 http://dx.doi.org/10.1093/nar/gku159 |
work_keys_str_mv | AT maoyuanhui decipheringtherulesbywhichdynamicsofmrnasecondarystructureaffecttranslationefficiencyinsaccharomycescerevisiae AT liuhuiling decipheringtherulesbywhichdynamicsofmrnasecondarystructureaffecttranslationefficiencyinsaccharomycescerevisiae AT liuyanlin decipheringtherulesbywhichdynamicsofmrnasecondarystructureaffecttranslationefficiencyinsaccharomycescerevisiae AT taoshiheng decipheringtherulesbywhichdynamicsofmrnasecondarystructureaffecttranslationefficiencyinsaccharomycescerevisiae |