3D Structure of the Human Genome Decoded

The research was led by scientists from Harvard University (Cambridge, MA, USA), the Broad Institute of Harvard and MIT (Cambridge, MA, USA), University of Massachusetts (UMass) Medical School (Boston, MA, USA), and the Massachusetts Institute of Technology (MIT; Cambridge, MA, USA).

"We've long known that on a small scale, DNA is a double helix,” said cofirst author Erez Lieberman-Aiden, a graduate student in the Harvard-MIT Division of Health Science and Technology and a researcher at Harvard's School of Engineering and Applied Sciences and in the laboratory of Dr. Eric Lander at the Broad Institute. "But if the double helix didn't fold further, the genome in each cell would be two meters-long. Scientists have not really understood how the double helix folds to fit into the nucleus of a human cell, which is only about a hundredth of a millimeter in diameter. This new approach enabled us to probe exactly that question.”

The researchers reported two remarkable findings. First, the human genome is organized into two separate compartments, keeping active genes separate and accessible while impounding unused DNA in a denser storage compartment. Chromosomes wind in and out of the two compartments repeatedly as their DNA alternates between active, gene-rich and inactive, gene-poor stretches. "Cells cleverly separate the most active genes into their own special neighborhood, to make it easier for proteins and other regulators to reach them,” stated Dr. Job Dekker, associate professor of biochemistry and molecular pharmacology at UMass Medical School and a senior author of the study.

Second, at a finer scale, the genome adopts an unusual organization known in mathematics as a "fractal.” The specific architecture the scientists found, called a "fractal globule,” enables the cell to bunch DNA incredibly tightly--the information density in the nucleus is trillions of times higher than on a computer chip--while avoiding the knots and tangles that might interfere with the cell's ability to read its own genome. Moreover, the DNA can easily unfold and refold during gene activation, gene repression, and cell replication.

"Nature's devised a stunningly elegant solution to storing information--a super-dense, knot-free structure,” said senior author Dr. Lander, director of the Broad Institute, who is also professor of biology at MIT, and professor of systems biology at Harvard Medical School.

In the past, many scientists had believed that DNA was compressed into a different architecture called an "equilibrium globule,” a configuration that is problematic because it can become densely knotted. The fractal globule architecture, while proposed as a theoretic possibility more than 20 years ago, has never previously been observed.

Critical to the current research was the development of the new Hi-C technique, which permits genome-wide analysis of the proximity of individual genes. The scientists first used formaldehyde to link together DNA strands that are nearby in the cell's nucleus. They then determined the identity of the neighboring segments by shredding the DNA into many tiny pieces, attaching the linked DNA into small loops, and performing massively parallel DNA sequencing.

"By breaking the genome into millions of pieces, we created a spatial map showing how close different parts are to one another,” remarked cofirst author Dr. Nynke van Berkum, a postdoctoral researcher at UMass Medical School in Dekker's laboratory. "We made a fantastic three-dimensional jigsaw puzzle and then, with a computer, solved the puzzle.”

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