Atomic-level, 3-D structure of MUTYH protein opens small window into DNA repair mechanism

Atomic-level, 3-D structure of MUTYH protein opens small window into DNA repair mechanism
MUTYH (cyan) binds to DNA (yellow) and recognizes 8-oxoguanine (red). A magnified view on the right shows the recognition mode of 8-oxoguanine (magenta) by MUTYH. Credit: Kumamoto University

Researchers have analyzed the three-dimensional structure of a protein that suppresses the development of colorectal polyposis, MUTYH, at the atomic level and clarified the repair mechanism for DNA mispairings by MUTYH. Since mutations in the MUTYH gene cause heritable colorectal polyposis, which leads to colorectal cancer, the researchers expect that this work will be useful for future research on heritable colorectal polyposis associated with MUTYH.

Reactive oxygen species produced inside cells oxidize DNA, and when the guanine base in DNA undergoes oxidation, 8-oxoguanine base is produced. Normally, guanine pairs with cytosine, but 8-oxoguanine also pairs with adenine, causing mutations that can lead to cancer and other aging-related diseases.

MUTYH is a protein that finds and removes adenine that has been mispaired with 8-oxoguanine. Mutations in its gene are known to cause heritable colorectal polyposis which can lead to . Furthermore, the repair efficiency of MUTYH increases when it interacts with PCNA, a protein involved in DNA replication, but the repair mechanisms at the have not been clarified.

To understand the function of a protein, it is important to know its structure at the atomic level. X-ray crystallography is a method that allows us to observe the molecules of living organisms at a scale of 1 x 10-10 m. Using this method, a research group led by Kumamoto University (Japan) has determined the X-ray crystal structure of MUTYH bound to a mispairing in DNA and the X-ray crystal structure of MUTYH bound to PCNA. Their analysis showed how MUTYH binds to the DNA double helix and searches for adenine:8-oxoguanine mispairings in DNA. Based on the three-dimensional structures of PCNA and MUTYH, the researchers proposed that PCNA serves as a clamp on the DNA and recruits MUTYH to the mispair site, which would clarify the mechanism by which MUTYH and PCNA cooperate to repair DNA. Furthermore, analysis of the 3D structure of MUTYH and DNA showed that mutations in the MUTYH gene reduce the binding affinity of MUTYH to DNA and destabilize the 3D structure of MUTYH, which leads to a decrease of its DNA repair activity.

  • Atomic-level, 3-D structure of MUTYH protein opens small window into DNA repair mechanism
    PCNA (pink) recruits MUTYH (cyan) to DNA (yellow) by the interaction between PCNA and MUTYH. Credit: Kumamoto University
  • Atomic-level, 3-D structure of MUTYH protein opens small window into DNA repair mechanism
    The positions for DNA binding and for stabilization of the 3D structure are shown in red and blue, respectively. Credit: Kumamoto University

"Since MUTYH and PCNA are known to work with various proteins involved in DNA repair, the three-dimensional structures that we clarified in this study should serve as a basis for further understanding the DNA repair mechanisms centered around MUTYH and PCNA," said Associate Professor Teruya Nakamura, who led the study. "We expect that the clarification of their atomic-level structures will be useful for future studies of heritable colorectal polyposis associated with MUTYH."

This research was posted online in Nucleic Acids Research on 18 June 2021.


Explore further

Electrical wire properties of DNA linked to cancer

More information: Teruya Nakamura et al, Structure of the mammalian adenine DNA glycosylase MUTYH: insights into the base excision repair pathway and cancer, Nucleic Acids Research (2021). DOI: 10.1093/nar/gkab492
Journal information: Nucleic Acids Research

Citation: Atomic-level, 3-D structure of MUTYH protein opens small window into DNA repair mechanism (2021, August 2) retrieved 24 September 2021 from https://phys.org/news/2021-08-atomic-level-d-mutyh-protein-small.html
This document is subject to copyright. Apart from any fair dealing for the purpose of private study or research, no part may be reproduced without the written permission. The content is provided for information purposes only.
82 shares

Feedback to editors