Forum for Science, Industry and Business

Sponsored by:     3M 
Search our Site:


Scientists are first to observe the global motions of an enzyme copying DNA

Scientists here have identified how the motions of an enzyme are related to correctly copying genetic instructions, setting the stage for studies that can uncover what happens when DNA copying mistakes are made.

Perpetuation of DNA mistakes can cause mutations that lead to cancer and other diseases.

But before scientists can determine how and when errors are made during DNA replication, they must first fully understand what’s going on when the copying process works properly – a monumental research pursuit that remains incomplete.

The Ohio State University researchers are the first to observe real-time behavior of all four sections, or domains, of an enzyme called Dpo4, a model Y-family enzyme.

The research defines critical steps in the process that starts when the enzyme binds to the correct nucleotide and ends when that nucleotide is put in place to become part of the string of molecules that compose a copied strand of DNA.

“Gaining insight into complex DNA transactions is fundamental to understanding the molecular basis of disease,” said senior study author Zucai Suo, associate professor of biochemistry and an investigator in the Ohio State University Comprehensive Cancer Center.

In the study, fluorescent markers on the enzyme’s sections showed how three of four components of Dpo4 tighten their grip on the DNA to achieve precise alignment while a nucleotide is added. The sections then relax their grip.

By looking at all four pieces of this enzyme in real time, the scientists may already have uncovered one clue about how DNA mistakes are made. The unexpected movement of one of those four pieces – called the little finger domain – in an opposite direction suggests this domain could make room for DNA mistakes to slip through the process.

“By moving away from the DNA, the additional space on the enzyme’s active site may accommodate a distorted DNA structure,” Suo said. “We are investigating that possibility now.”

The research appears online today (10/27) in the journal PLoS Biology, published by the Public Library of Science.

Human cells contain enzymes – called polymerases – that perform the process of copying DNA. The double helix of the DNA contains the genetic instructions for building an organism, and when cells in any living being divide, they copy DNA to pass on those instructions to new cells.

During this replication, the two halves of the DNA strand separate, and each half becomes a template for a new partner. The polymerases are responsible for “reading” the templates to determine where to place nucleotides to create the matching partners – resulting in the creation of two identical double helices.

Polymerases are divided among six families of enzymes based on their amino acid sequence and function: A, B, C, D, X and Y (the most recently discovered family).

The A family has been well-studied and takes care of most of the DNA copying. But enzymes in this family stall if they come across DNA damage, and that stalling endangers the replication process and could lead to cell death.

The Y family of polymerases, on the other hand, can step in to bypass damage and allow copying to continue. This keeps the cell alive but also has led scientists to wonder if these enzymes could also be a major source of mistakes.

Polymerases are attractive research subjects because they have already been used as targets in anti-cancer and anti-viral drugs, so fully understanding their behavior could open up avenues for further drug development, noted Jessica Brown, a doctoral student in the Ohio State Biochemistry Program and a co-author of the study.

“In the case of polymerases, you want to know how these dynamics relate to the correct nucleotide incorporation so you can then determine the dynamics when the wrong molecule is incorporated,” Brown said.

The research group used an enzyme called Dpo4, or DNA polymerase IV, for the experiments. Before now, scientists had determined crystal structures of relationships between this enzyme and DNA that represented their relationship frozen at a single point in time.

To see the interactions in real time, Suo and colleagues were the first to insert fluorescent markers into each of the four components of the enzyme – called the palm, thumb, finger and little finger. They also placed markers in a strand of DNA. Previous studies have emphasized just one enzyme domain at a time.

The polymerase interacts with DNA to start the copying process in the presence of a nucleotide – in this case, a molecule called dNTP. The scientists used fluorescence resonance energy transfer technology to see the action take place.

They described the process as a series of eight critical steps that proceed with three distinct movements in the presence of a dNTP. The enzyme stands alone until it binds to DNA. The enzyme and DNA undergo repositioning when the nucleotide binds to the polymerase, and the enzyme’s domains begin to move, gripping the template DNA strand. The DNA strand must move from what is known as the pocket to allow binding and incorporation of the nucleotide in the correct place.

By step five in the process, the DNA copy has been extended, and in the following steps the enzyme begins its relaxation motions – allowing the DNA to shift to allow for placement of the next nucleotide.

Those who study DNA polymerases seek to define what is called a rate-limiting event, which could be thought of as a moment when all parts of the process pause and check themselves over. Because errors occur in the DNA copying process, the rate-limiting step must be known to completely understand the copying mechanism, Suo noted.

To date, scientists have believed that the rate-limiting step in this process occurred long before the placement of the nucleotide. To check this, Suo and colleagues applied mathematical equations to the fluorescently lit observations to assign time frames to each part of the process.

They determined that the rate-limiting step of dNTP placement occurs during a brief and subtle shift of amino acids that ensures correct alignment of all structures just before the nucleotide is placed.

The rate-limiting step also requires the most energy of any step in the dNTP placement process. Suo and colleagues measured energy requirements for the key steps preceding placement of the nucleotide and found that the step requiring the most energy is that same subtle alignment shift.

The Suo lab is now using these findings and the fluorescent marking system to explore the dynamics of replication when DNA is damaged.

This work is supported by a National Science Foundation Career Award, the National Institutes of Health and an American Heart Association Predoctoral Fellow grant.

Additional co-authors of the study are Cuiling Xu, a postdoctoral researcher in Ohio State’s Department of Biochemistry, Brian Maxwell, a graduate student in the Ohio State Biophysics Program, and Likui Zhang, a former visiting scholar in biochemistry.

Contact: Zucai Suo, (614) 688-3706; or Jessica Brown, (614) 247-6832;

Written by Emily Caldwell, (614) 292-8310;

Zucai Suo | EurekAlert!
Further information:

More articles from Life Sciences:

nachricht North and South Cooperation to Combat Tuberculosis
22.03.2018 | Universität Zürich

nachricht Researchers Discover New Anti-Cancer Protein
22.03.2018 | Universität Basel

All articles from Life Sciences >>>

The most recent press releases about innovation >>>

Die letzten 5 Focus-News des innovations-reports im Überblick:

Im Focus: Researchers Discover New Anti-Cancer Protein

An international team of researchers has discovered a new anti-cancer protein. The protein, called LHPP, prevents the uncontrolled proliferation of cancer cells in the liver. The researchers led by Prof. Michael N. Hall from the Biozentrum, University of Basel, report in “Nature” that LHPP can also serve as a biomarker for the diagnosis and prognosis of liver cancer.

The incidence of liver cancer, also known as hepatocellular carcinoma, is steadily increasing. In the last twenty years, the number of cases has almost doubled...

Im Focus: Researchers at Fraunhofer monitor re-entry of Chinese space station Tiangong-1

In just a few weeks from now, the Chinese space station Tiangong-1 will re-enter the Earth's atmosphere where it will to a large extent burn up. It is possible that some debris will reach the Earth's surface. Tiangong-1 is orbiting the Earth uncontrolled at a speed of approx. 29,000 km/h.Currently the prognosis relating to the time of impact currently lies within a window of several days. The scientists at Fraunhofer FHR have already been monitoring Tiangong-1 for a number of weeks with their TIRA system, one of the most powerful space observation radars in the world, with a view to supporting the German Space Situational Awareness Center and the ESA with their re-entry forecasts.

Following the loss of radio contact with Tiangong-1 in 2016 and due to the low orbital height, it is now inevitable that the Chinese space station will...

Im Focus: Alliance „OLED Licht Forum“ – Key partner for OLED lighting solutions

Fraunhofer Institute for Organic Electronics, Electron Beam and Plasma Technology FEP, provider of research and development services for OLED lighting solutions, announces the founding of the “OLED Licht Forum” and presents latest OLED design and lighting solutions during light+building, from March 18th – 23rd, 2018 in Frankfurt a.M./Germany, at booth no. F91 in Hall 4.0.

They are united in their passion for OLED (organic light emitting diodes) lighting with all of its unique facets and application possibilities. Thus experts in...

Im Focus: Mars' oceans formed early, possibly aided by massive volcanic eruptions

Oceans formed before Tharsis and evolved together, shaping climate history of Mars

A new scenario seeking to explain how Mars' putative oceans came and went over the last 4 billion years implies that the oceans formed several hundred million...

Im Focus: Tiny implants for cells are functional in vivo

For the first time, an interdisciplinary team from the University of Basel has succeeded in integrating artificial organelles into the cells of live zebrafish embryos. This innovative approach using artificial organelles as cellular implants offers new potential in treating a range of diseases, as the authors report in an article published in Nature Communications.

In the cells of higher organisms, organelles such as the nucleus or mitochondria perform a range of complex functions necessary for life. In the networks of...

All Focus news of the innovation-report >>>



Industry & Economy
Event News

Virtual reality conference comes to Reutlingen

19.03.2018 | Event News

Ultrafast Wireless and Chip Design at the DATE Conference in Dresden

16.03.2018 | Event News

International Tinnitus Conference of the Tinnitus Research Initiative in Regensburg

13.03.2018 | Event News

Latest News

Modular safety concept increases flexibility in plant conversion

22.03.2018 | Trade Fair News

New interactive map shows climate change everywhere in world

22.03.2018 | Earth Sciences

New technologies and computing power to help strengthen population data

22.03.2018 | Earth Sciences

Science & Research
Overview of more VideoLinks >>>