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Teasing Apart Translational and Transcriptional Components of Stochastic Variations in Eukaryotic Gene Expression
The intrinsic stochasticity of gene expression leads to cell-to-cell variations, noise, in protein abundance. Several processes, including transcription, translation, and degradation of mRNA and proteins, can contribute to these variations. Recent single cell analyses of gene expression in yeast hav...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3431295/ https://www.ncbi.nlm.nih.gov/pubmed/22956896 http://dx.doi.org/10.1371/journal.pcbi.1002644 |
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author | Salari, Raheleh Wojtowicz, Damian Zheng, Jie Levens, David Pilpel, Yitzhak Przytycka, Teresa M. |
author_facet | Salari, Raheleh Wojtowicz, Damian Zheng, Jie Levens, David Pilpel, Yitzhak Przytycka, Teresa M. |
author_sort | Salari, Raheleh |
collection | PubMed |
description | The intrinsic stochasticity of gene expression leads to cell-to-cell variations, noise, in protein abundance. Several processes, including transcription, translation, and degradation of mRNA and proteins, can contribute to these variations. Recent single cell analyses of gene expression in yeast have uncovered a general trend where expression noise scales with protein abundance. This trend is consistent with a stochastic model of gene expression where mRNA copy number follows the random birth and death process. However, some deviations from this basic trend have also been observed, prompting questions about the contribution of gene-specific features to such deviations. For example, recent studies have pointed to the TATA box as a sequence feature that can influence expression noise by facilitating expression bursts. Transcription-originated noise can be potentially further amplified in translation. Therefore, we asked the question of to what extent sequence features known or postulated to accompany translation efficiency can also be associated with increase in noise strength and, on average, how such increase compares to the amplification associated with the TATA box. Untangling different components of expression noise is highly nontrivial, as they may be gene or gene-module specific. In particular, focusing on codon usage as one of the sequence features associated with efficient translation, we found that ribosomal genes display a different relationship between expression noise and codon usage as compared to other genes. Within nonribosomal genes we found that sequence high codon usage is correlated with increased noise relative to the average noise of proteins with the same abundance. Interestingly, by projecting the data on a theoretical model of gene expression, we found that the amplification of noise strength associated with codon usage is comparable to that of the TATA box, suggesting that the effect of translation on noise in eukaryotic gene expression might be more prominent than previously appreciated. |
format | Online Article Text |
id | pubmed-3431295 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-34312952012-09-06 Teasing Apart Translational and Transcriptional Components of Stochastic Variations in Eukaryotic Gene Expression Salari, Raheleh Wojtowicz, Damian Zheng, Jie Levens, David Pilpel, Yitzhak Przytycka, Teresa M. PLoS Comput Biol Research Article The intrinsic stochasticity of gene expression leads to cell-to-cell variations, noise, in protein abundance. Several processes, including transcription, translation, and degradation of mRNA and proteins, can contribute to these variations. Recent single cell analyses of gene expression in yeast have uncovered a general trend where expression noise scales with protein abundance. This trend is consistent with a stochastic model of gene expression where mRNA copy number follows the random birth and death process. However, some deviations from this basic trend have also been observed, prompting questions about the contribution of gene-specific features to such deviations. For example, recent studies have pointed to the TATA box as a sequence feature that can influence expression noise by facilitating expression bursts. Transcription-originated noise can be potentially further amplified in translation. Therefore, we asked the question of to what extent sequence features known or postulated to accompany translation efficiency can also be associated with increase in noise strength and, on average, how such increase compares to the amplification associated with the TATA box. Untangling different components of expression noise is highly nontrivial, as they may be gene or gene-module specific. In particular, focusing on codon usage as one of the sequence features associated with efficient translation, we found that ribosomal genes display a different relationship between expression noise and codon usage as compared to other genes. Within nonribosomal genes we found that sequence high codon usage is correlated with increased noise relative to the average noise of proteins with the same abundance. Interestingly, by projecting the data on a theoretical model of gene expression, we found that the amplification of noise strength associated with codon usage is comparable to that of the TATA box, suggesting that the effect of translation on noise in eukaryotic gene expression might be more prominent than previously appreciated. Public Library of Science 2012-08-30 /pmc/articles/PMC3431295/ /pubmed/22956896 http://dx.doi.org/10.1371/journal.pcbi.1002644 Text en © 2012 This is an open-access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Salari, Raheleh Wojtowicz, Damian Zheng, Jie Levens, David Pilpel, Yitzhak Przytycka, Teresa M. Teasing Apart Translational and Transcriptional Components of Stochastic Variations in Eukaryotic Gene Expression |
title | Teasing Apart Translational and Transcriptional Components of Stochastic Variations in Eukaryotic Gene Expression |
title_full | Teasing Apart Translational and Transcriptional Components of Stochastic Variations in Eukaryotic Gene Expression |
title_fullStr | Teasing Apart Translational and Transcriptional Components of Stochastic Variations in Eukaryotic Gene Expression |
title_full_unstemmed | Teasing Apart Translational and Transcriptional Components of Stochastic Variations in Eukaryotic Gene Expression |
title_short | Teasing Apart Translational and Transcriptional Components of Stochastic Variations in Eukaryotic Gene Expression |
title_sort | teasing apart translational and transcriptional components of stochastic variations in eukaryotic gene expression |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3431295/ https://www.ncbi.nlm.nih.gov/pubmed/22956896 http://dx.doi.org/10.1371/journal.pcbi.1002644 |
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