Cargando…
Quantitating translational control: mRNA abundance-dependent and independent contributions and the mRNA sequences that specify them
Translation rate per mRNA molecule correlates positively with mRNA abundance. As a result, protein levels do not scale linearly with mRNA levels, but instead scale with the abundance of mRNA raised to the power of an ‘amplification exponent’. Here we show that to quantitate translational control, th...
Autores principales: | , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5714229/ https://www.ncbi.nlm.nih.gov/pubmed/29040683 http://dx.doi.org/10.1093/nar/gkx898 |
_version_ | 1783283550569627648 |
---|---|
author | Li, Jingyi Jessica Chew, Guo-Liang Biggin, Mark D. |
author_facet | Li, Jingyi Jessica Chew, Guo-Liang Biggin, Mark D. |
author_sort | Li, Jingyi Jessica |
collection | PubMed |
description | Translation rate per mRNA molecule correlates positively with mRNA abundance. As a result, protein levels do not scale linearly with mRNA levels, but instead scale with the abundance of mRNA raised to the power of an ‘amplification exponent’. Here we show that to quantitate translational control, the translation rate must be decomposed into two components. One, TR(mD), depends on the mRNA level and defines the amplification exponent. The other, TR(mIND), is independent of mRNA amount and impacts the correlation coefficient between protein and mRNA levels. We show that in Saccharomyces cerevisiae TR(mD) represents ∼20% of the variance in translation and directs an amplification exponent of 1.20 with a 95% confidence interval [1.14, 1.26]. TR(mIND) constitutes the remaining ∼80% of the variance in translation and explains ∼5% of the variance in protein expression. We also find that TR(mD) and TR(mIND) are preferentially determined by different mRNA sequence features: TR(mIND) by the length of the open reading frame and TR(mD) both by a ∼60 nucleotide element that spans the initiating AUG and by codon and amino acid frequency. Our work provides more appropriate estimates of translational control and implies that TR(mIND) is under different evolutionary selective pressures than TR(mD). |
format | Online Article Text |
id | pubmed-5714229 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-57142292017-12-08 Quantitating translational control: mRNA abundance-dependent and independent contributions and the mRNA sequences that specify them Li, Jingyi Jessica Chew, Guo-Liang Biggin, Mark D. Nucleic Acids Res Genomics Translation rate per mRNA molecule correlates positively with mRNA abundance. As a result, protein levels do not scale linearly with mRNA levels, but instead scale with the abundance of mRNA raised to the power of an ‘amplification exponent’. Here we show that to quantitate translational control, the translation rate must be decomposed into two components. One, TR(mD), depends on the mRNA level and defines the amplification exponent. The other, TR(mIND), is independent of mRNA amount and impacts the correlation coefficient between protein and mRNA levels. We show that in Saccharomyces cerevisiae TR(mD) represents ∼20% of the variance in translation and directs an amplification exponent of 1.20 with a 95% confidence interval [1.14, 1.26]. TR(mIND) constitutes the remaining ∼80% of the variance in translation and explains ∼5% of the variance in protein expression. We also find that TR(mD) and TR(mIND) are preferentially determined by different mRNA sequence features: TR(mIND) by the length of the open reading frame and TR(mD) both by a ∼60 nucleotide element that spans the initiating AUG and by codon and amino acid frequency. Our work provides more appropriate estimates of translational control and implies that TR(mIND) is under different evolutionary selective pressures than TR(mD). Oxford University Press 2017-11-16 2017-10-11 /pmc/articles/PMC5714229/ /pubmed/29040683 http://dx.doi.org/10.1093/nar/gkx898 Text en Published by Oxford University Press on behalf of Nucleic Acids Research 2017. This work is written by (a) US Government employee(s) and is in the public domain in the US. |
spellingShingle | Genomics Li, Jingyi Jessica Chew, Guo-Liang Biggin, Mark D. Quantitating translational control: mRNA abundance-dependent and independent contributions and the mRNA sequences that specify them |
title | Quantitating translational control: mRNA abundance-dependent and independent contributions and the mRNA sequences that specify them |
title_full | Quantitating translational control: mRNA abundance-dependent and independent contributions and the mRNA sequences that specify them |
title_fullStr | Quantitating translational control: mRNA abundance-dependent and independent contributions and the mRNA sequences that specify them |
title_full_unstemmed | Quantitating translational control: mRNA abundance-dependent and independent contributions and the mRNA sequences that specify them |
title_short | Quantitating translational control: mRNA abundance-dependent and independent contributions and the mRNA sequences that specify them |
title_sort | quantitating translational control: mrna abundance-dependent and independent contributions and the mrna sequences that specify them |
topic | Genomics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5714229/ https://www.ncbi.nlm.nih.gov/pubmed/29040683 http://dx.doi.org/10.1093/nar/gkx898 |
work_keys_str_mv | AT lijingyijessica quantitatingtranslationalcontrolmrnaabundancedependentandindependentcontributionsandthemrnasequencesthatspecifythem AT chewguoliang quantitatingtranslationalcontrolmrnaabundancedependentandindependentcontributionsandthemrnasequencesthatspecifythem AT bigginmarkd quantitatingtranslationalcontrolmrnaabundancedependentandindependentcontributionsandthemrnasequencesthatspecifythem |