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Motasem ElGamel

Publications and source records attributed to Motasem ElGamel.

4 recordsLinked to original sources

Optimal information transmission in a sequential model for cell division

In proliferating cell populations, adaptive changes to biochemical reactions can change a cell's division time, which in turn can change the population size. However, biochemical reactions are subject to noise, and therefore the conditions for optimal information transmission from the molecular to the population scale are poorly understood. Here, we model cell proliferation as a Bellman-Harris branching process with age-dependent division times. We identify a class of division time distributions, built from a series of Markovian steps, for which the population size distribution at all times is hierarchically calculable. We use this feature to characterize the amount of influence that a given reaction step has on the population size via the mutual information. We find that information transmission is optimal for a characteristic number of steps until division: too few and the population size is unpredictable; too many and any given step has vanishing influence on the population size. Our work reveals the potential tradeoffs involved in adaptive decision making at the sub-cellular, cellular and population scales.

physics.bio-ph

General mechanism for concentration-based cell size control

Cells control their size to cope with noise during growth and division. Eukaryotic cells exhibiting "sizer" control (targeting a specific size before dividing) may rely on molecular concentration thresholds, but simple implementations of this strategy are not stable. We derive a general criterion for concentration-based sizer control and demonstrate it with a mechanistic model that resolves the instability by using multistage progression towards division. We show that if molecular dynamics in one stage satisfy the sizer criterion, then sizer control follows for the whole progression. We predict that perturbations to the molecular dynamics in non-sizer stages shift the size statistics without disrupting sizer control, consistent with recent experiments in fission yeast.

physics.bio-ph

Effects of molecular noise on cell size control

Cells employ control strategies to maintain a stable size. Dividing at a target size (the `sizer' strategy) is thought to produce the tightest size distribution. However, this result follows from phenomenological models that ignore the molecular mechanisms required to implement the strategy. Here we investigate a simple mechanistic model for exponentially growing cells whose division is triggered at a molecular abundance threshold. We find that size noise inherits the molecular noise and is consequently minimized not by the sizer but by the `adder' strategy, where a cell divides after adding a target amount to its birth size. We derive a lower bound on size noise that agrees with publicly available data from six microfluidic studies on Escherichia coli bacteria.

physics.bio-ph

Multigenerational memory in bacterial size control

Cells maintain a stable size as they grow and divide. Inspired by the available experimental data, most proposed models for size homeostasis assume size control mechanisms that act on a timescale of one generation. Such mechanisms lead to short-lived autocorrelations in size fluctuations that decay within less than two generations. However, recent evidence from comparing sister lineages suggests that correlations in size fluctuations can persist for many generations. Here we develop a minimal model that explains these seemingly contradictory results. Our model proposes that different environments result in different control parameters, leading to distinct inheritance patterns. Multigenerational memory is revealed in constant environments but obscured when averaging over many different environments. Inferring the parameters of our model from {\it Escherichia coli} size data in microfluidic experiments, we recapitulate the observed statistics. Our work elucidates the impact of the environment on cell homeostasis and growth and division dynamics.

physics.bio-ph