Abstract

Genetically identical cells exposed to homogeneous environment can show remarkable phenotypic difference. To predict how phenotype is shaped, understanding of how each factor contributes is required. During gene expression processes, noise could arise either intrinsically in biochemical processes of gene expression or extrinsically from other cellular processes such as cell growth. In this work, important noise sources in gene expression of phage λ lysogen are quantified using models described by stochastic differential equations (SDEs). Results show that DNA looping has sophisticated impacts on gene expression noise: When DNA looping provides autorepression, like in wild type, it reduces noise in the system; When the autorepression is defected as it is in certain mutants, DNA looping increases expression noise. We also study how each gene operator affects the expression noise by changing the binding affinity between the gene and the transcription factor systematically. We find that the system shows extraordinarily large noise when the binding affinity is in certain range, which changes the system from monostable to bistable. In addition, we find that cell growth causes non-negligible noise, which increases with gene expression level. Quantification of noise and identification of new noise sources will provide deeper understanding on how stochasticity impacts phenotype.

Highlights

  • In this work, phage λ is used to study gene expression noise

  • In our previous work[4] on quantifying noise of cI expression with chemical Langevin equations (CLEs)[29], we simplified the expression processes by integrating transcription and translation into one virtual process, resulting in a system the state of which can be described by the birth-death process of protein CI

  • We present a model considering noise from mRNA fluctuation in addition to that from protein fluctuation, which we refer to as two-step expression model

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Summary

Lysogenic Phage Lambda

Identical cells exposed to homogeneous environment can show remarkable phenotypic difference. Gene expression noise in E. coli has been widely studied, which gave quantifications of intrinsic and extrinsic noise of dynamics and of steady states, from single cell to population[11,16,17,18,19], revealing a number of factors that affect gene expression noise in E. coli, including gene regulation, fluctuation of transcription rate[11] and of protein production rate[19]. These factors could play a role in phage λ system. We focus on the population fluctuation from an ensemble view and give the mathematical definition of each noise. (2) How and how significantly each noise factor affects gene expression

Results
Parameter δ mRNA NDNA μ Nns
Discussion
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