Search Results (5)

A mutator is a variant in a population of organisms whose mutation rate is higher than the average mutation rate in the population. For genetic and population dynamics reasons, mutators are produced and survive with much greater frequency than anti-mutators (variants with a lower-than-average mutation rate). This strong asymmetry is a consequence of both fundamental genetics and natural selection; it can lead to a ratchet-like increase in the mutation rate. The rate at which mutators appear is, therefore, a parameter that should be of great interest to evolutionary biologists generally; for example, it can influence: (1) the survival duration of a species, especially asexual species (which are known to be short-lived), (2) the evolution of recombination, a process that can ameliorate the deleterious effects of mutator abundance, (3) the rate at which cancer appears, (4) the ability of pathogens to escape immune surveillance in their hosts, (5) the long-term fate of mitochondria, etc. In spite of its great relevance to basic and applied science, the rate of mutation to a mutator phenotype continues to be essentially unknown. The reasons for this gap in our knowledge are largely methodological; in general, a mutator phenotype cannot be observed directly, but must instead be inferred from the numbers of some neutral “marker” mutation that can be observed directly: different mutation-rate variants will produce this marker mutation at different rates. Here, we derive the expected distribution of the numbers of the marker mutants observed, accounting for the fact that some of the mutants will have been produced by a mutator phenotype that itself arose by mutation during the growth of the culture. These developments, together with previous enhancements of the Luria–Delbrück assay (by one of us, dubbed the “Jones protocol”), make possible a novel experimental protocol for estimating the rate of mutation to a mutator phenotype. Simulated experiments using biologically reasonable parameters that employ this protocol show that such experiments in the lab can give us fairly accurate estimates of the rate of mutation to a mutator phenotype. Although our ability to estimate mutation-to-mutator rates from simulated experiments is promising, we view this study as a proof-of-concept study and an important first step towards practical empirical estimation. Full article

While Luria and Delbrück’s seminal work has found its way to some college biology textbooks, it is now largely absent from those in mathematics. This is a significant omission, and we consider it a missed opportunity to present a celebrated conceptual model that provides an authentic and, in many ways, intuitive example of the quantifiable nature of stochasticity. We argue that it is an important topic that could enrich the educational literature in mathematics, from the introductory to advanced levels, opening many doors to undergraduate research. The paper has two main parts. First, we present in detail the mathematical theory behind the Luria–Delbrück model and make suggestions for further readings from the literature. We also give ideas for inclusion in various mathematics courses and for projects that can be used in regular courses, independent projects, or as starting points for student research. Second, we briefly review available hands-on activities as pedagogical ways to facilitate problem posing, problem-based learning, and investigative case-based learning and to expose students to experiments leading to Poisson distributions. These help students with even limited mathematics backgrounds understand the significance of Luria–Delbrück’s work for determining mutation rates and its impact on many fields, including cancer chemotherapy, antibiotic resistance, radiation, and environmental screening for mutagens and teratogens. Full article

We consider a fluctuation test experiment in which cell colonies were grown from a single cell until they reach a given population size and were then exposed to treatment. While they grow, the cells may, with a low probability, acquire resistance to treatment and pass it on to their offspring. Unlike the classical Luria–Delbrück fluctuation test, and motivated by recent work on drug-resistance acquisition in cancer/microbial cells, we allowed the resistant cell state to switch back to a drug-sensitive state. This modification did not affect the central part of the Luria–Delbrück distribution of the number of resistant survivors: the previously developed approximation by the Landau probability density function applied. However, the right tail of the modified distribution deviated from the power law decay of the Landau distribution. Here, we demonstrate that the correction factor was equal to the Landau cumulative distribution function. We interpreted the appearance of the Landau laws from the standpoint of singular perturbation theory and used the asymptotic matching principle to construct uniformly valid approximations. Additionally, we describe the corrections to the distribution tails in populations initially consisting of multiple sensitive cells, a mixture of sensitive and resistant cells, and a cell with a randomly drawn state. Full article

Originating from the Luria–Delbrück experiment in 1943, fluctuation analysis (FA) has been well developed to demonstrate random mutagenesis in microbial cell populations and infer mutation rates. Despite the remarkable progress in its theory and applications, FA often faces difficulties in the computation perspective, due to the lack of appropriate simulators. Existing simulation algorithms are usually designed specifically for particular scenarios, thus their applications may be largely restricted. There is a pressing need for more flexible simulators that rely on minimum model assumptions and are highly adaptable to produce data for a wide range of scenarios. In this study, we propose SimuBP, a simulator of population dynamics and mutations based on branching processes. SimuBP generates data based on a general two-type branching process, which is able to mimic the real cell proliferation and mutation process. Through simulations under traditional FA assumptions, we demonstrate that the data generated by SimuBP follow expected distributions, and exhibit high consistency with those generated by two alternative simulators. The most impressive feature of SimuBP lies in its flexibility, which enables the simulation of data analogous to real fluctuation experiments. We demonstrate the application of SimuBP through examples of estimating mutation rates. Full article

Concepts of infinitely divisible distributions are reviewed and applied to mutant number distributions derived from the Lea-Coulson and other models which describe the Luria-Delbrück fluctuation test. A key finding is that mutant number distributions arising from a generalised Lea-Coulson model for which normal cell growth is non-decreasing are unimodal. An integral criterion is given which separates the cases of a mode at the origin, or not. Full article