bioRxiv ScienceSearch

Biology subjects

Mazzolini, A.

Publications and source records attributed to Mazzolini, A..

2 recordsLinked to original sources

Emergent Statistical Laws in Single-Cell Transcriptomic Data

Large scale data on single-cell gene expression have the potential to unravel the specific transcriptional programs of different cell types. The structure of these expression datasets suggests a similarity with several other complex systems that can be analogously described through the statistics of their basic building blocks. Transcriptomes of single cells are collections of messenger RNA abundances transcribed from a common set of genes just as books are different collections of words from a shared vocabulary, genomes of different species are specific compositions of genes belonging to evolutionary families, and ecological niches can be described by their species abundances. Following this analogy, we identify several emergent statistical laws in single-cell transcriptomic data closely similar to regularities found in linguistics, ecology or genomics. A simple mathematical framework can be used to analyze the relations between different laws and the possible mechanisms behind their ubiquity. Importantly, treatable statistical models can be useful tools in transcriptomics to disentangle the actual biological variability from general statistical effects present in most component systems and from the consequences of the sampling process inherent to the experimental technique. Author summaryGene expression profiles represent how different cells use their genetic information. Similarly, books are specific collections of words chosen from a shared vocabulary, and many complex systems can be ultimately described by the statistics of their basic components. Leveraging on this analogy, we identified several emergent statistical laws in single-cell transcriptomic data that are universally found in complex component systems. A simple mathematical description sets these laws in a treatable quantitative framework and represents a useful tool for dissecting the different sources of gene expression variability.

systems biology

Universality of evolutionary dynamics with arbitrary demography

The assumption of constant population size is central in population genetics. It led to a large body of results, that are robust to modeling choices and that have proven successful to understand evolutionary dynamics. In reality, allele frequencies and population size are both determined by the interaction between a population and the environment. Relaxing the constant-population assumption have two big drawbacks. It increases the technical difficulty of the analysis, and it requires specifying a mechanism for the saturation of the population size, possibly making the results contingent on model details. Here, we develop a framework that encompasses a great variety of systems with an arbitrary mechanism for population growth limitation. By using techniques based on scale separation for stochastic processes, we are able to calculate analytically properties of evolutionary trajectories, such as the fixation probability. Remarkably, these properties assume a universal form with respect to our framework, which depends on only three parameters related to the inter-generation timescale, the invasion fitness, and the carrying capacity of the strains. In other words, different systems, such as Lotka-Volterra or a chemostat model (contained in our framework), share the same evolutionary outcomes after a proper re-mapping of their parameters. An important and surprising consequence of our results is that the direction of selection can be inverted, with a population evolving to reach lower values of invasion fitness.

evolutionary biology