Biology subjects

Mohammad Soltani

Publications and source records attributed to Mohammad Soltani.

3 recordsLinked to original sources

bioRxiv2016

Cell-cycle coupled expression minimizes random fluctuations in gene product levels

Expression of many genes varies as a cell transitions through different cell-cycle stages. How coupling between stochastic expression and cell cycle impacts cell-to-cell variability (noise) in the level of protein is not well understood. We analyze a model, where a stable protein is synthesized in random bursts, and the frequency with which bursts occur varies within the cell cycle. Formulas quantifying the extent of fluctuations in the protein copy number are derived and decomposed into components arising from the cell cycle and stochastic processes. The latter stochastic component represents contributions from bursty expression and errors incurred during partitioning of molecules between daughter cells. These formulas reveal an interesting trade-off: cell-cycle dependencies that amplify the noise contribution from bursty expression also attenuate the contribution from partitioning errors. We investigate existence of optimum strategies for coupling expression to the cell cycle that minimize the stochastic component. Intriguingly, results show that a zero production rate throughout the cell cycle, with expression only occurring just before cell division minimizes noise from bursty expression for a fixed mean protein level. In contrast, the optimal strategy in the case of partitioning errors is to make the protein just after cell division. We provide examples of regulatory proteins that are expressed only towards the end of cell cycle, and argue that such strategies enhance robustness of cell-cycle decisions to the intrinsic stochasticity of gene expression.

Systems Biology↗

bioRxiv2015

Stochastic Analysis Of An Incoherent Feedforward Genetic Motif

Gene products (RNAs, proteins) often occur at low molecular counts inside individual cells, and hence are subject to considerable random fluctuations (noise) in copy number over time. Not surprisingly, cells encode diverse regulatory mechanisms to buffer noise. One such mechanism is the incoherent feedforward circuit. We analyze a simplistic version of this circuit, where an upstream regulator X affects both the production and degradation of a protein Y. Thus, any random increase in Xs copy numbers would increase both production and degradation, keeping Y levels unchanged. To study its stochastic dynamics, we formulate this network into a mathematical model using the Chemical Master Equation formulation. We prove that if the functional dependence of Ys production and degradation on X is similar, then the steady-distribution of Ys copy numbers is independent of X. To investigate how fluctuations in Y propagate downstream, a protein Z whose production rate only depend on Y is introduced. Intriguingly, results show that the extent of noise in Z increases with noise in X, in spite of the fact that the magnitude of noise in Y is invariant of X. Such counter intuitive results arise because X enhances the time-scale of fluctuations in Y, which amplifies fluctuations in downstream processes. In summary, while feedforward systems can buffer a protein from noise in its upstream regulators, noise can propagate downstream due to changes in the time-scale of fluctuations.

Molecular Biology↗

bioRxiv2015

Decomposing variability in protein levels from noisy expression, genome duplication and partitioning errors during cell-divisions

Inside individual cells, expression of genes is inherently stochastic and manifests as cell-to-cell variability or noise in protein copy numbers. Since proteins half-lives can be comparable to the cell-cycle length, randomness in cell-division times generates additional intercellular variability in protein levels. Moreover, as many mRNA/protein species are expressed at low-copy numbers, errors incurred in partitioning of molecules between the mother and daughter cells are significant. We derive analytical formulas for the total noise in protein levels for a general class of cell-division time and partitioning error distributions. Using a novel hybrid approach the total noise is decomposed into components arising from i) stochastic expression; ii) partitioning errors at the time of cell-division and iii) random cell-division events. These formulas reveal that random cell-division times not only generate additional extrinsic noise but also critically affect the mean protein copy numbers and intrinsic noise components. Counter intuitively, in some parameter regimes noise in protein levels can decrease as cell-division times become more stochastic. Computations are extended to consider genome duplication, where the gene dosage is increased by two-fold at a random point in the cell-cycle. We systematically investigate how the timing of genome duplication influences different protein noise components. Intriguingly, results show that noise contribution from stochastic expression is minimized at an optimal genome duplication time. Our theoretical results motivate new experimental methods for decomposing protein noise levels from single-cell expression data. Characterizing the contributions of individual noise mechanisms will lead to precise estimates of gene expression parameters and techniques for altering stochasticity to change phenotype of individual cells.

Systems Biology↗