Mesoscale phase separation of chromatin in the nucleus

Intact-organism imaging of Drosophila larvae reveals and quantifies chromatin-aqueous phase separation. The chromatin can be organized near the lamina layer of the nuclear envelope, conventionally fill the nucleus, be organized centrally, or as a wetting droplet. These transitions are controlled by changes in nuclear volume and the interaction of chromatin with the lamina (part of the nuclear envelope) at the nuclear periphery. Using a simple polymeric model that includes the key features of chromatin self-attraction and its binding to the lamina, we demonstrate theoretically that it is the competition of these two effects that determines the mode of chromatin distribution. The qualitative trends as well as the composition profiles obtained in our simulations compare well with the observed intact-organism imaging and quantification. Since the simulations contain only a small number of physical variables we can identify the generic mechanisms underlying the changes in the observed phase separations.

Automated summary

Intact-organism imaging of Drosophila larvae reveals and quantifies chromatin-aqueous phase separation, with different chromatin distributions controlled by nuclear volume changes and chromatin-lamina interaction. Theoretical models show that the competition between chromatin self-attraction and its binding to the lamina determines the distribution mode. Simulations with few physical variables can identify generic mechanisms underlying observed phase separations.