In multicellular organisms, every cell contains nearly identical genetic information. However, there is an amazing diversity of cell types that perform varieties of functions. Cellular identity and differentiation is therefore not determined by the DNA sequence itself but by the expression of selected genomic regions in time and space. At the molecular level, these transcriptional programs are controlled by so-called epigenetic processes guiding each single cell towards its own fate. Failures in epigenetic pathways are often at the heart of human diseases such as cancer. Furthermore, reprogramming the genome using epigenetic tools is rapidly emerging as powerful approach to improve human health or plant fitness. The research in the Bischof lab aims at understanding the role of the epigenome on a cell’s behavior, ultimately paving the way for improving both human health and agriculture.

We primarily use the plant model Arabidopsis thaliana as it offers considerable advantages and opportunities to perform cutting-edge research. It has a small size and short generation time, is amenability for genetic transformation and offers easy genetics. Its trim and well-annotated genome allows comprehensive and cost-efficient genomics. Most importantly, the high tolerance of plant genomes to genomic instability, often lethal in other model organisms, represents a fascinating opportunity to tackle essential aspects of biology. This genomic robustness therefore enables mutagenesis-driven forward genetic screens to discover new pathways that control the genome. Finally, due to the high degree of conservation of molecular mechanisms between organisms, our findings and methodology are not limited to understanding chromatin dynamics in plants, but have implications beyond the scope of plant biology.