Welcome to the new version of CaltechAUTHORS. Login is currently restricted to library staff. If you notice any issues, please email coda@library.caltech.edu
Published January 2012 | Published + Supplemental Material
Journal Article Open

A Genome-Wide Analysis of Promoter-Mediated Phenotypic Noise in Escherichia coli

Abstract

Gene expression is subject to random perturbations that lead to fluctuations in the rate of protein production. As a consequence, for any given protein, genetically identical organisms living in a constant environment will contain different amounts of that particular protein, resulting in different phenotypes. This phenomenon is known as "phenotypic noise." In bacterial systems, previous studies have shown that, for specific genes, both transcriptional and translational processes affect phenotypic noise. Here, we focus on how the promoter regions of genes affect noise and ask whether levels of promoter-mediated noise are correlated with genes' functional attributes, using data for over 60% of all promoters in Escherichia coli. We find that essential genes and genes with a high degree of evolutionary conservation have promoters that confer low levels of noise. We also find that the level of noise cannot be attributed to the evolutionary time that different genes have spent in the genome of E. coli. In contrast to previous results in eukaryotes, we find no association between promoter-mediated noise and gene expression plasticity. These results are consistent with the hypothesis that, in bacteria, natural selection can act to reduce gene expression noise and that some of this noise is controlled through the sequence of the promoter region alone

Additional Information

© 2012 Silander et al. 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 credited. Received August 22, 2011; Accepted November 16, 2011; Published January 19, 2012. OKS, NN, and MA were supported by a grant from the Swiss National Science Foundation to MA. OKS was additionally supported by an Ambizione fellowship from the Swiss National Foundation. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript. We thank T. Bollenbach for sharing bacterial strains, R. Beiko for sharing data on horizontal transfer, E. van Nimwegen for valuable discussions, and three reviewers for helpful comments on the manuscript. Author Contributions: Conceived and designed the experiments: OKS NN MA AZ. Performed the experiments: OKS NN AZ AB IK. Analyzed the data: OKS NN MA. Contributed reagents/materials/analysis tools: AZ AB IK UA. Wrote the paper: OKS NN MA.

Attached Files

Published - Silander2012p17511Plos_Genet.pdf

Supplemental Material - journal.pgen.1002443.s001.pdf

Supplemental Material - journal.pgen.1002443.s002.pdf

Supplemental Material - journal.pgen.1002443.s003.pdf

Supplemental Material - journal.pgen.1002443.s004.pdf

Supplemental Material - journal.pgen.1002443.s005.pdf

Supplemental Material - journal.pgen.1002443.s006.pdf

Supplemental Material - journal.pgen.1002443.s007.pdf

Supplemental Material - journal.pgen.1002443.s008.pdf

Supplemental Material - journal.pgen.1002443.s009.doc

Supplemental Material - journal.pgen.1002443.s010.xls

Supplemental Material - journal.pgen.1002443.s011

Files

Silander2012p17511Plos_Genet.pdf
Files (2.8 MB)
Name Size Download all
md5:4ca2c1b39c4f8e22915298d91b9e1f62
1.2 MB Preview Download
md5:8b09b165b8982d06b560532ed438dee0
183.7 kB Preview Download
md5:a68b213bead04aa735ab62e7724524bc
220.5 kB Preview Download
md5:40916f6168c3298c053bd40f4a129436
88.2 kB Preview Download
md5:35544eb422e101f1c4c25f9ff42f6925
146.1 kB Preview Download
md5:084711cbd09e530d11e5105e6703c0fa
85.7 kB Preview Download
md5:0b32c6b97804e8ded214f30e323b9858
252.7 kB Preview Download
md5:70638fff3ec2f94a78d8b048d54fe275
99.8 kB Download
md5:66b53f612a7b4c4c9fec078c736cb6c2
283.6 kB Download
md5:89c27d1beb305167582cae605dde41c4
205.0 kB Preview Download
md5:0be99444bb3be3700b3f9d189c015500
101.9 kB Preview Download
md5:d9869c46c2570cce1ee27901c3b29352
1.9 kB Download

Additional details

Created:
August 19, 2023
Modified:
October 24, 2023