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.

Encounter times of chromatin loci influenced by polymer decondensation.

The time for a DNA sequence to find its homologous counterpart depends on a long random search inside the cell nucleus. Using polymer models, we compute here the mean first encounter time (MFET) between two sites located on two different polymer chains and confined locally by potential wells. We find that reducing tethering forces acting on the polymers results in local decondensation, and numerical simulations of the polymer model show that these changes are associated with a reduction of the MFET by several orders of magnitude. We derive here new asymptotic formula for the MFET, confirmed by Brownian simulations. We conclude from the present modeling approach that the fast search for homology is mediated by a local chromatin decondensation due to the release of multiple chromatin tethering forces. The present scenario could explain how the homologous recombination pathway for double-stranded DNA repair is controlled by its random search step.

Polymer model with long-range interactions: analysis and applications to the chromatin structure.

Chromatin inside the cell nucleus consists of the DNA and its hierarchy of interacting molecules, which can be modeled as a complex polymer. To describe the chromatin dynamic, we develop and analyze here a polymer model that accounts for long-range interactions and not just those between the closest neighbors as in the Rouse polymer model. Our construction of the polymer model allows us to recover the local interaction between monomers from the anomalous diffusion exponent, which can be directly measured experimentally. We compute asymptotically for this polymer model the cross-correlation function for a given monomer and the mean time for a loop to be formed. Finally, we discuss some possible applications for interpretation of chromosome capture data.

Diffusing polymers in confined microdomains and estimation of chromosomal territory sizes from chromosome capture data.

Is it possible to extract the size and structure of chromosomal territories (confined domain) from the encounter frequencies of chromosomal loci? To answer this question, we estimate the mean time for two monomers located on the same polymer to encounter, which we call the mean first encounter time in a confined microdomain (MFETC). We approximate the confined domain geometry by a harmonic potential well and obtain an asymptotic expression that agrees with Brownian simulations for the MFETC as a function of the polymer length, the radius of the confined domain, and the activation distance radius ε at which the two searching monomers meet. We illustrate the present approach using chromosome capture data for the encounter rate distribution of two loci depending on their distances along the DNA. We estimate the domain size that restricts the motion of one of these loci for chromosome II in yeast.

Computation of the mean first-encounter time between the ends of a polymer chain.

Using a novel theoretical approach, we study the mean first-encounter time (MFET) between the two ends of a polymer. Previous approaches used various simplifications that reduced the complexity of the problem, leading, however, to incompatible results. We construct here for the first time a general theory that allows us to compute the MFET. The method is based on estimating the mean time for a Brownian particle to reach a narrow domain in the polymer configuration space. In dimension two and three, we find that the MFET depends mainly on the first eigenvalue of the associated Fokker-Planck operator and provide precise estimates that are confirmed by Brownian simulations. Interestingly, although many time scales are involved in the encounter process, its distribution can be well approximated by a single exponential, which has several consequences for modeling chromosome dynamics in the nucleus. Another application of our result is computing the mean time for a DNA molecule to form a closed loop (when its two ends meet for the first time).

Encounter dynamics of a small target by a polymer diffusing in a confined domain.

We study the first passage time for a polymer, that we call the narrow encounter time (NETP), to reach a small target located on the surface of a microdomain. The polymer is modeled as a freely joint chain (beads connected by springs with a resting non zero length) and we use Brownian simulations to study two cases: when (i) any of the monomer or (ii) only one can be absorbed at the target window. Interestingly, we find that in the first case, the NETP is an increasing function of the polymer length until a critical length, after which it decreases. Moreover, in the long polymer regime, we identified an exponential scaling law for the NETP as a function of the polymer length. In the second case, the position of the absorbed monomer along the polymer chain strongly influences the NETP. Our analysis can be applied to estimate the mean first time of a DNA fragment to a small target in the chromatin structure or for mRNA to find a small target.

Molecular analysis of noroviruses involved in acute gastroenteritis outbreaks in military units in Israel, 1999-2004.

The study presented here was conducted to determine the genetic properties of noroviruses (NoVs) identified between 1999 and 2004 in army recruits with acute gastroenteritis. Partial sequence analysis of the RNA-dependent RNA polymerase gene revealed the presence of two major sub-genogroups, all of which were related to genogroup II of NoV. Serological analysis using recombinant antigens confirmed this observation. Local strains associated with a 1999 outbreak were closely related to GII-6 strains, while those identified later were very closely related to GII-4 strains. GII-4 strains were also associated with an outbreak in civilian nursing homes in Israel in 2002 and samples from this outbreak were included in this study for comparison. This is the first report describing the molecular properties of NoV strains associated with diarrhea-related morbidity in Israel.