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      Noise in transcription negative feedback loops: simulation and experimental analysis

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          Abstract

          Negative feedback loops have been invoked as a way to control and decrease transcriptional noise. Here, we have built three circuits to test the effect of negative feedback loops on transcriptional noise of an autoregulated gene encoding a transcription factor (TF) and a downstream gene (DG), regulated by this TF. Experimental analysis shows that self-repression decreases noise compared to expression from a non-regulated promoter. Interestingly enough, we find that noise minimization by negative feedback loop is optimal within a range of repression strength. Repression values outside this range result in noise increase producing a U-shaped behaviour. This behaviour is the result of external noise probably arising from plasmid fluctuations as shown by simulation of the network. Regarding the target gene of a self-repressed TF (sTF), we find a strong decrease of noise when repression by the sTF is strong and a higher degree of noise anti-correlation between sTF and its target. Simulations of the circuits indicate that the main source of noise in these circuits could come from plasmid variation and therefore that negative feedback loops play an important role in suppressing both external and internal noise. An important observation is that DG expression without negative feedback exhibits bimodality at intermediate TF repression values. This bimodal behaviour seems to be the result of external noise as it can only be found in those simulations that include plasmid variation.

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          Partitioning of lipid-modified monomeric GFPs into membrane microdomains of live cells.

          Many proteins associated with the plasma membrane are known to partition into submicroscopic sphingolipid- and cholesterol-rich domains called lipid rafts, but the determinants dictating this segregation of proteins in the membrane are poorly understood. We suppressed the tendency of Aequorea fluorescent proteins to dimerize and targeted these variants to the plasma membrane using several different types of lipid anchors. Fluorescence resonance energy transfer measurements in living cells revealed that acyl but not prenyl modifications promote clustering in lipid rafts. Thus the nature of the lipid anchor on a protein is sufficient to determine submicroscopic localization within the plasma membrane.
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            Noise propagation in gene networks.

            Accurately predicting noise propagation in gene networks is crucial for understanding signal fidelity in natural networks and designing noise-tolerant gene circuits. To quantify how noise propagates through gene networks, we measured expression correlations between genes in single cells. We found that noise in a gene was determined by its intrinsic fluctuations, transmitted noise from upstream genes, and global noise affecting all genes. A model was developed that explains the complex behavior exhibited by the correlations and reveals the dominant noise sources. The model successfully predicts the correlations as the network is systematically perturbed. This approach provides a step toward understanding and manipulating noise propagation in more complex gene networks.
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              New unstable variants of green fluorescent protein for studies of transient gene expression in bacteria.

              Use of the green fluorescent protein (Gfp) from the jellyfish Aequorea victoria is a powerful method for nondestructive in situ monitoring, since expression of green fluorescence does not require any substrate addition. To expand the use of Gfp as a reporter protein, new variants have been constructed by the addition of short peptide sequences to the C-terminal end of intact Gfp. This rendered the Gfp susceptible to the action of indigenous housekeeping proteases, resulting in protein variants with half-lives ranging from 40 min to a few hours when synthesized in Escherichia coli and Pseudomonas putida. The new Gfp variants should be useful for in situ studies of temporal gene expression.
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                Author and article information

                Journal
                Mol Syst Biol
                Molecular Systems Biology
                1744-4292
                2006
                01 August 2006
                : 2
                : 41
                Affiliations
                [1 ] European Molecular Biology Laboratory (EMBL), Heildelberg, Germany
                Author notes
                [a ] European Molecular Biology Laboratory (EMBL), SCB, Meyerhofstrasse 1, 69117 Heildelberg, Germany. Tel.: +49 6 221387320; Fax: +49 6 221387306; E-mail: serrano@ 123456embl.de
                [*]

                These authors contributed equally to this work

                Article
                msb4100081
                10.1038/msb4100081
                1681513
                16883354
                f6c5a7af-4114-4464-a786-2a2c903759e1
                Copyright © 2006, EMBO and Nature Publishing Group
                History
                : 11 January 2006
                : 14 June 2006
                Page count
                Pages: 1
                Categories
                Article

                Quantitative & Systems biology
                smartcell,negative feedback loop,autoregulation,noise,tetr
                Quantitative & Systems biology
                smartcell, negative feedback loop, autoregulation, noise, tetr

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