Advances Using Single-Particle Trajectories to Reconstruct Chromatin Organization and Dynamics

Chromatin organization remains complex and far from understood. In this article, we review recent statistical methods of extracting biophysical parameters from in vivo single-particle trajectories of loci to reconstruct chromatin reorganization in response to cellular stress such as DNA damage. We look at methods for analyzing both single locus and multiple loci tracked simultaneously and explain how to quantify and describe chromatin motion using a combination of extractable parameters. These parameters can be converted into information about chromatin dynamics and function. Furthermore, we discuss how the timescale of recurrent encounter between loci can be extracted and interpreted. We also discuss the effect of sampling rate on the estimated parameters. Finally, we review a polymer method to reconstruct chromatin structure using crosslinkers between chromatin sites. We list and refer to some software packages that are now publicly available to simulate polymer motion. To conclude, chromatin organization and dynamics can be reconstructed from locus trajectories and predicted based on polymer models. Chromatin organization and dynamics can be reconstructed from loci trajectories. Biophysical parameters are often extracted from single chromatin loci single-particle trajectories (SPTs).Statistical methods are being used to study the dynamics of multiple chromatin loci.Chromatin properties can be described by polymer models.Available packages exist for coarse-graining chromatin reconstruction.