
Stretched out completely, a human chromosome would be several centimeters long. It is packed, along with its 45 companions, into a few-microns-wide cell nucleus in such a way that all the necessary genes are accessible to RNA transcription. Figuring out how that packing is done is no easy task. Microscopy helps, but provides nowhere near a complete picture. Now a research team led by Eric Lander of MIT and Job Dekker of the University of Massachusetts has developed a method for probing chromosomes’ folded structures. The researchers chemically join segments of a folded chromosome that are close in space, cut away and sequence the DNA around the crosslink, and compare those sequences to genome libraries to determine which parts of the chromosome are in contact. A matrix of the observed contacts, as shown in the figure, reveals large-scale organization. Analyzing the plaid pattern, the researchers found that most of the cell’s actively transcribed DNA was spatially segregated from most of the inactive DNA. On a smaller scale, chromosome segments a millimeter or so in extended length appeared to form so-called fractal globules with self-similar structures very different from that of a tangled polymer in equilibrium. So far, the researchers have studied only cultured cell lines: one derived from a tumor and another modified by a virus. They hope to apply their method to healthy cells and to look for differences in chromosome structure among cells of different types. (E. Lieberman-Aiden et al., Science 326, 289, 2009.) —Johanna Miller
Synchronized oscillatory processes in populations of living cells can arise in two ways. In one type of transition, individual cells oscillate out of synchrony at low number density and gradually synchronize as their density is increased. In another type, cells exhibit no oscillations at low density, but above a threshold density they suddenly begin oscillating in synchrony. Biological systems' complexity makes understanding the transition mechanisms a challenge. But now, researchers led by
Soft biological tissue is often subjected to forces that affect the tissue’s geometry, and finite elasticity provides a robust theoretical framework for analyzing the mechanical behavior of those tissues. Although the theory can accommodate anisotropic, nonlinear, and inhomogeneous processes subjected to large stresses and strains, its complexity makes many problems intractable. For growing tissue, though, the slow addition of cells generates shape- or size-changing stresses that are small enough to model successfully (see PHYSICS TODAY, April 2007,
Theorists have long predicted that scattering materials, such as milk and white paint, contain transparent channels that light can pass right through. Ordinarily, very little of the light in an incident beam enters those so-called open channels, and the materials appear opaque. But it should be possible to create a shaped wave that couples more light into the open channels. In fact, Ivo Vellekoop and Allard Mosk of the University of Twente in the Netherlands have done just that. Last year, they demonstrated a method for shaping a light wave, by tuning the relative phases of segments of their beam, so that much of the light transmitted through their scattering sample would be focused to a point. (See PHYSICS TODAY, October 2007,