The researchers found that, contrary to how it’s depicted in most textbooks, chromatin does not fold in on itself in an organized manner to create distinct structures. Instead, it forms a pliable, inconsistent chain characterized by a wide variety of folding patterns.
“We show that chromatin does not need to form discrete higher-order structures to fit in the nucleus,” explains O’Shea in a news release by the Salk.
DNA winds itself around histone proteins. Eight histones, together with their associated DNA, form nucleosomes, which are then folded up and condensed several more times into a chromatid. But according to the report, scientists haven’t actually seen how DNA folds into chromatids within whole cells.
A team of scientists at the Salk Institute applied a new dye that covers the surface of DNA, and together with University of California, San Diego, researchers, used electron-microscope tomography to visualize its 3-D structure, dubbing their method ChromEMT.
“The system enables individual DNA particles, chains and chromosomes to be visualized in 3D in a live, single cell. Thus, we are able to see the fine structure and interactions of DNA and chromatin in the nucleus of intact, live cells,” senior author Clodagh O'Shea of the Salk Institute says in a news release by the National Institutes of Health (NIH), which funded the study.
This new picture of chromatin structure demonstrates that in order to contain itself within a given cell’s nucleus, DNA folds a bit differently than what researchers originally envisioned. The authors conclude that chromatin is both “a flexible and disordered 5- to 24-nm-diameter granular chain that is packed together at different concentration densities.” It bends and folds together in different places, achieving a diversity of structures.