FSU Researchers Unravel Mystery of How, When DNA Replicates


  • newswise-fullscreen FSU Researchers Unravel Mystery of How, When DNA Replicates

    Credit: Bruce Palmer/FSU Photography Services

    David Gilbert is the J. Herbert Taylor Distinguished Professor of Molecular Biology

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Dec. 27, 2018

FSU RESEARCHERS UNRAVEL MYSTERY OF HOW, WHEN DNA REPLICATES

Newswise — TALLAHASSEE, Fla. — A team of Florida State University researchers has unlocked a decades-old mystery about how a critical cellular process is regulated and what that could mean for the future study of genetics.

In cells, DNA and its associated material replicate at regular intervals, a process essential to all living organisms. This contributes to everything from how the body responds to disease to hair color. DNA replication was identified in the late 1950s, but since then researchers across the globe have come up short trying to understand exactly how this process was regulated.

Now they know.

David Gilbert, the J. Herbert Taylor Distinguished Professor of Molecular Biology, and doctoral student Jiao Sima published a paper today in the journal Cell that showed there are specific points along the DNA molecule that control replication.

“It’s been quite a mystery,” Gilbert said. “Replication seemed resilient to everything we tried to do to perturb it. We’ve described it in detail, shown it changes in different cell types and that it is disrupted in disease. But until now, we couldn’t find that final piece, the control elements or the DNA sequences that control it.”

Notably, Gilbert’s professorship is in honor of a former Florida State professor named J. Herbert Taylor. Taylor demonstrated how different segments of chromosomes duplicate in the late 1950s and published more than 100 papers on chromosome structure and replication. Roughly 60 years later, Gilbert determined how replication was regulated.

Sima had been working with Gilbert in the lab and ran close to a hundred genetic mutations on DNA molecules, hoping to see some sort of result that would better explain how the replication process worked. At a point of frustration, Gilbert said they came up with a “hail Mary” attempt.

Gilbert and Sima examined a single segment of the DNA in the highest possible 3D resolution and saw three sequences along the DNA molecule touching each other frequently. The researchers then used CRISPR, a sophisticated gene editing technology, to remove these three areas simultaneously.

And with that, they found that these three elements together were the key to DNA replication.

“Removing these elements shifted the segment’s replication time from the very beginning to the very end of the process,” Gilbert said. “This was one of those moments where just one result knocks your socks off.”

In addition to the effect on replication timing, the removal of the three elements caused the 3D structure of the DNA molecule to change dramatically.

“We have for the first time pinpointed specific DNA sequences in the genome that regulate chromatin structure and replication timing,” Sima said. “These results reflect one possible model of how DNA folds inside cells and how these folding patterns could impact the hereditary materials’ function.”

Greater understanding of how DNA replication is regulated opens new paths of research in genetics. When replication timing is altered — as it was in Gilbert and Sima’s experiment — it can completely change how the genetic information of a cell is interpreted.

This could become crucial information as scientists tackle complicated diseases where the replication timing is disrupted.

“If you duplicate at a different place and time, you might assemble a completely different structure,” Gilbert said. “A cell has different things available to it at different times. Changing when something replicates changes the packaging of the genetic information.”

This research was supported by the National Institutes of Health.

Other researchers from Florida State University contributed to this study, as well as scientists from La Jolla Institute for Allergy and Immunology, the Babraham Institute, the University of Michigan, the Gladstone Institute of Cardiovascular Disease and Roddenberry Center for Stem Cell Biology and Medicine, University of California San Francisco and Charité Universitätsmedizin Berlin.

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