scholarly journals Quantifying Extrinsic Noise in Gene Expression Using the Maximum Entropy Framework

2013 ◽  
Vol 104 (12) ◽  
pp. 2743-2750 ◽  
Author(s):  
Purushottam D. Dixit
Cell Reports ◽  
2019 ◽  
Vol 26 (13) ◽  
pp. 3752-3761.e5 ◽  
Author(s):  
Antoine Baudrimont ◽  
Vincent Jaquet ◽  
Sandrine Wallerich ◽  
Sylvia Voegeli ◽  
Attila Becskei

2019 ◽  
Author(s):  
Lucy Ham ◽  
Rowan D. Brackston ◽  
Michael P.H. Stumpf

AbstractNoise in gene expression is one of the hallmarks of life at the molecular scale. Here we derive analytical solutions to a set of models describing the molecular mechanisms underlying transcription of DNA into RNA. Our Ansatz allows us to incorporate the effects of extrinsic noise – encompassing factors external to the transcription of the individual gene – and discuss the ramifications for heterogeneity in gene product abundance that has been widely observed in single cell data. Crucially, we are able to show that heavy-tailed distributions of RNA copy numbers cannot result from the intrinsic stochasticity in gene expression alone, but must instead reflect extrinsic sources of variability.


2017 ◽  
Vol 50 (1) ◽  
pp. 15092-15096 ◽  
Author(s):  
Aarón Vázquez-Jiménez ◽  
Moisés Santillán ◽  
Jesús Rodríguez-González

2020 ◽  
Vol 48 (16) ◽  
pp. 9406-9413 ◽  
Author(s):  
Tyler Quarton ◽  
Taek Kang ◽  
Vasileios Papakis ◽  
Khai Nguyen ◽  
Chance Nowak ◽  
...  

Abstract Eukaryotic protein synthesis is an inherently stochastic process. This stochasticity stems not only from variations in cell content between cells but also from thermodynamic fluctuations in a single cell. Ultimately, these inherently stochastic processes manifest as noise in gene expression, where even genetically identical cells in the same environment exhibit variation in their protein abundances. In order to elucidate the underlying sources that contribute to gene expression noise, we quantify the contribution of each step within the process of protein synthesis along the central dogma. We uncouple gene expression at the transcriptional, translational, and post-translational level using custom engineered circuits stably integrated in human cells using CRISPR. We provide a generalized framework to approximate intrinsic and extrinsic noise in a population of cells expressing an unbalanced two-reporter system. Our decomposition shows that the majority of intrinsic fluctuations stem from transcription and that coupling the two genes along the central dogma forces the fluctuations to propagate and accumulate along the same path, resulting in increased observed global correlation between the products.


2014 ◽  
Vol 24 (10) ◽  
pp. 1698-1706 ◽  
Author(s):  
Eilon Sharon ◽  
David van Dijk ◽  
Yael Kalma ◽  
Leeat Keren ◽  
Ohad Manor ◽  
...  

mSphere ◽  
2019 ◽  
Vol 4 (3) ◽  
Author(s):  
João P. N. Silva ◽  
Soraia Vidigal Lopes ◽  
Diogo J. Grilo ◽  
Zach Hensel

ABSTRACTSome microbiology experiments and biotechnology applications can be improved if it is possible to tune the expression of two different genes at the same time with cell-to-cell variation at or below the level of genes constitutively expressed from the chromosome (the “extrinsic noise limit”). This was recently achieved for a single gene by exploiting negative autoregulation by the tetracycline repressor (TetR) and bicistronic gene expression to reduce gene expression noise. We report new plasmids that use the same principles to achieve simultaneous, low-noise expression for two genes inEscherichia coli. The TetR system was moved to a compatible plasmid backbone, and a system based on thelacrepressor (LacI) was found to also exhibit gene expression noise below the extrinsic noise limit. We characterized gene expression mean and noise across the range of induction levels for these plasmids, applied the LacI system to tune expression for single-molecule mRNA detection under two different growth conditions, and showed that two plasmids can be cotransformed to independently tune expression of two different genes.IMPORTANCEMicrobiologists often express foreign proteins in bacteria in order study them or to use bacteria as a microbial factory. Usually, this requires controlling the number of foreign proteins expressed in each cell, but for many common protein expression systems, it is difficult to “tune” protein expression without large cell-to-cell variation in expression levels (called “noise” in protein expression). This work describes two protein expression systems that can be combined in the same cell, with tunable expression levels and very low protein expression noise. One new system was used to detect single mRNA molecules by fluorescence microscopy, and the two systems were shown to be independent of each other. These protein expression systems may be useful in any experiment or biotechnology application that can be improved with low protein expression noise.


2015 ◽  
Vol 11 (5) ◽  
pp. 805 ◽  
Author(s):  
Sanjay Tyagi

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