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遺伝学 DNA 鎖

デルフト工科大学の研究者は、DNA 複製における分子モーター CMG を組み立てて画像化する新しい方法を開発し、これまでにない解像度と複製プロセスへの洞察を提供しています。 この進歩により、遺伝性疾患やがんの発生についての理解が深まる可能性があります。

Nature Communications, will pave the way for further discoveries in the study of DNA replication.

DNA replication is fundamental to life, as the faithful transmission of genetic information between generations of cells is crucial for the survival and health of all living organisms. It is carried out by an intricate cellular machinery, known as the replisome, that is made up of protein building blocks. A key component of this machinery is CMG, the molecular motor that powers the replisome during DNA replication. 

CMG has the important task of separating the two strands of the DNA double helix, so that the message that they encode can be read and copied. “Understanding how CMG moves along DNA is crucial for our understanding of DNA replication,” says Daniel Ramírez Montero, researcher and first author of the publication. Studying DNA replication is very important because errors in this process can lead to genetic disorders or cancer.

Motor of DNA Replication Experimental Setup

Diagram of the experimental setup: (Top) Schematic of a CMG-containing DNA molecule held in place with optical tweezers (red beams) while a scanning laser (green beam) is taking a picture of it; CMG motors are depicted in blue. (Bottom) Actual image of a fluorescently labelled CMG molecular motor (green spot) on an unlabelled DNA molecule held in place with optical tweezers. Credit: Adapted from Ramirez Montero, et al, Nature Communications, 2023

Motion on film

In living cells, CMG is assembled and activated via an intricate cascade of biochemical reactions that involves 36 different proteins. A group of TU Delft researchers led by Spinoza laureate Professor Nynke Dekker, in collaboration with Francis Crick Institute group leader Dr. John Diffley, has developed a way to carry out this tightly controlled process outside of the cell and measure the motion of individual CMG molecular motors. The researchers extracted all 36 proteins from cells to build up CMG on DNA. By attaching fluorescent labels to some of the proteins, they could directly observe the movement of the CMG molecular motor under a fluorescent microscope. 

“With this new approach, we were able to visualize the motion of individual CMGs made from scratch. We used optical tweezers to hold the CMG-containing DNA still for easier visualization, and then took movies of CMG as it moved along the DNA. This way, we could measure its motion at the single-molecule level for the first time,” explains Ramírez Montero. 

CMG Motors Moving Along DNA Molecule

Example of CMG motors moving along a DNA molecule held in place by an optical trap. Credit: Taken from Ramírez Montero, et al., Nature Communications, 2023.

New insights

Using their bottom-up approach, which combines cutting-edge biochemistry and biophysics, the group of researchers was able to directly visualize the motion of individual CMG motors assembled from scratch for the first time, and measure this motion with unprecedented resolution. In addition, they made the unexpected discovery that CMG can move randomly along the DNA when a key molecule called ATP is absent; furthermore, they show that subsequent re-binding of ATP allows CMG to tightly hold onto the DNA, thereby halting its random motion. This halting is important, as it likely facilitates the activation of CMG, a critical process in the initiation of DNA replication. 

This work will pave the way for further studies that may uncover unknown details of key processes in DNA replication. These discoveries can in turn get us closer to understanding how cells manage to faithfully transmit their genetic information with every cell division, as well as to better understand the errors in the process that can contribute to the development of genetic disorders or cancer. Ramírez Montero: “Biological systems can look very complicated and chaotic at first sight, but by observing them at this resolution, we can understand the simple and elegant physics behind them.”

Reference: “Nucleotide binding halts diffusion of the eukaryotic replicative helicase during activation” by Daniel Ramírez Montero, Humberto Sánchez, Edo van Veen, Theo van Laar, Belén Solano, John F. X. Diffley and Nynke H. Dekker, 14 April 2023, Nature Communications.
DOI: 10.1038/s41467-023-37093-9

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