Laboratory Dominic Grün
Quantitative single cell biology
Substantial variability of mRNA levels across cells of the same type has been observed in any organism studied, ranging from bacteria and yeast to mammals. Gene expression variability can have diverse origins. Heterogeneity of cell states following extrinsic or intrinsic stimuli, e. g., due to cell cycle, metabolic fluctuations or differentiation events, can be one reason for cell-to-cell transcriptome differences. Moreover, many genes are presumably transcribed in bursts rather than at a constant rate, leading to substantially different transcript numbers in individual cells, commonly addressed as gene expression noise. Gene expression variability causes fluctuations in protein levels, and can entail physiological differences between cells.
In unicellular organisms, such as bacteria, yeast, and viruses, gene expression noise is utilized to increase heterogeneity of the population, permitting quick adjustment to fluctuating environments. In higher eukaryotes, the relevance and the regulation of gene expression noise are much less explored. Development of a multicellular organism requires robust execution of developmental transitions with spatial and temporal precision. Although the required cell differentiation events rely on coordinate execution of gene expression changes, mammalian genes have been found to exhibit strongly varying bursting kinetics. The magnitude of gene expression noise in mammalian cells is comparable to unicellular systems, i.e., mRNA levels frequently differ more than twofold between identical cells. However, the role of gene expression noise and its regulation during cellular differentiation on a genome-wide level are largely unexplored.
In our lab we investigate how stem cells robustly maintain their pluripotent state and reliably execute differentiation programs with spatial and temporal precision in the presence of gene expression noise. For this purpose we study in vitro differentiation of cell lines and 3D cell culture systems and analyze differentiation in animal models within collaborative projects.
Regulation of gene expression during cellular differentiation
To understand how gene expression is regulated during differentiation of a stem cell into all its daughter cell types one has to be able to discriminate distinct cell types and states in a complex mixture, such as a tissue or an organ. The established approach is profiling sub-populations of cells purified based on only a handful of marker genes. This pre-selection imposes strong constraints on the resolution of cell types. Moreover, measuring gene expression in populations of cells masks the true distribution of gene expression levels across cells.
Figure 1: Single cell mRNA sequencing is performed on randomly sampled cells from an organ to discover cell types and infer lineage trees. Mechanistic models of gene regulation during differentiation can be derived from these data.[less]
Figure 1: Single cell mRNA sequencing is performed on randomly sampled cells from an organ to discover cell types and infer lineage trees. Mechanistic models of gene regulation during differentiation can be derived from these data.
Single cell profiling, on the other hand, reveals an unbiased sample of all cell types in a complex mixture. The transcriptome of a cell can be looked at as a fingerprint revealing its identity. We use single cell mRNA sequencing to investigate the transcriptome and other molecular readouts such as DNA methylation and genomic DNA of individual cells. Our lab develops computational methods to infer cell types and differentiation trajectories from these data with the goal to derive high-resolution lineage trees and to understand dynamics of gene expression during cellular differentiation. We are particularly interested in rare cell types, since those are oftentimes overlooked and can have crucial functions. For example, the stem cells themselves often occur at low frequencies.
Our strategy will allow us to derive lineage trees de novo and to revise current models for cell differentiation in well-studied systems, such as the bone marrow. Moreover, marker genes for cell types and states can be identified with high specificity, which permits the purification of these cells and subsequent population based assays, e. g. ChiP-seq, to measure epigenetic marks and transcription factor binding. The ultimate goal is the derivation of a mechanistic model of gene regulation during differentiation by combining these population-based measurements with single cell gene expression data.
The role of biological gene expression noise during cellular differentiation
A specific focus of the lab is on the role of gene expression variability across single cells during differentiation. It has been shown that transcription is frequently not a continuous process but happens in bursts. This induces substantial cell-to-cell variability of mRNA levels, and the role of this so-called biological noise during cellular differentiation is not well understood.
Diffferentiation has to be a robust process with spatial and temporal precision and mechanisms for the control and utilization of gene expression noise are likely to exist.
Using single cell transcriptomics in conjunction with population based assays we try to elucidate how biological gene expression noise changes during differentiation and how it is mechanistically regulated. Since single cell sequencing still suffers from substantial technical noise we also utilize microscopic imaging of individual mRNAs in single cells (single molecule FISH) to investigate gene expression variability with high specificity and sensitivity.