Damaged DNA may stall patrolling molecule to initiate repair

Sites where DNA is damaged may cause a molecule that slides along the DNA strand to scan for damage to slow on its patrol, delaying it long enough to recognize and initiate repair. The finding suggests that the delay itself may be the key that allows the protein molecule to find its target, according to researchers at the University of Illinois at Chicago.

Usually, the repair protein zips along quickly, says Anjum Ansari, UIC professor of physics and co-principal investigator on the study, published this month in Nature Communications.

"If the DNA is normal and the protein is searching, the interaction that the protein makes with the DNA is not very tight, and the protein is able to wander at some speed," Ansari said.

"When the protein encounters a damaged DNA, it's not quite like a normal DNA , it may be a little twisted or more flexible. The protein 'stumbles' at that spot and gets a little stalled, enough to give it a little bit more time at the damaged site," she said. "The longer it sits, the higher the probability that it will open the DNA and initiate repair."

This 'stumble' gives the protein time to flip out the damaged nucleotide building blocks of the DNA and recruit other proteins that begin repair, said Jung-Hyun Min, assistant professor of chemistry at UIC and co-principal investigator on the study.

The protein, xeroderma pigmentosum C or XPC, is important for the repair of DNA damaged by environmental insults, like the chemicals in cigarette smoke and pollutants, which makes it important for preventing cancers, Min said. Dysfunctional XPC may lead to a 1,000-fold increase in the risk of skin cancer.

How the protein can find a lesion hidden among perhaps 100,000 times as many undamaged nucleotides has been a mystery, Min said. XPC is unusual in that it does not have a "pocket" that fits one specific damaged structure while rejecting others that do not fit well. Instead, it recognizes damage indirectly, and so is able to repair a variety of derangements.

In order to see how XPC distinguishes between normal and damaged DNA, the researchers used a chemical trick to bind the protein to a single site on intact DNA. To their surprise, they found that the protein flipped open the nucleotides on undamaged DNA just as it does at a bad spot.

The finding suggested that, if held in one place long enough, XPC could open even undamaged DNA. Using a technique called temperature-jump perturbation spectroscopy to observe the interaction of XPC with DNA in real time, the researchers determined that the protein needed several milliseconds to flip open DNA at a damaged site.

"We think it could take as much 4,000 times as long to open DNA at an undamaged versus damaged site," said Ansari. The XPC protein moves too quickly to engage undamaged DNA, but is stalled by a twisted damage site long enough to flip out the bad nucleotides and initiate repair.

This dependence on how quickly the protein could open up the DNA before moving on suggests an entirely new kind of binding-site recognition, said Min.

"This has a potential to explain the kind of phenomena that we couldn't explain before," Min said, such as how the protein turns up in some places where the DNA does not harbor damage that XPC would be expected to recognize on its own.

"This may be done, for example, through interactions with other proteins that can bring XPC there and stall it for a moment," she said. "It may be that all you need is to bring the protein to these sites and stall it for a moment."

The researchers believe that this "delay-triggered kinetic gating" could be a common mechanism among many other types of DNA recognition proteins.