A human MUTYH variant linking colonic polyposis to redox degradation of the [4Fe4S]2+ cluster.
Published Web Locationhttps://www.nature.com/articles/s41557-018-0068-x.epdf?author_access_token=x523-_7-j3mjJoIQrVrgNNRgN0jAjWel9jnR3ZoTv0PEJ3HJRtrWrafb6ROI51I-_oXJVpx6-nfzDQxkcDLIZVb_XpmP2ylJBfV3MqnmUe7N8m_VsxeNWHkJeX952xPVxcamR6ViT8UmKUTxE3Vqbw==
The human DNA repair enzyme MUTYH excises mispaired adenine residues in oxidized DNA. Homozygous MUTYH mutations underlie the autosomal, recessive cancer syndrome MUTYH-associated polyposis. We report a MUTYH variant, p.C306W (c.918C>G), with a tryptophan residue in place of native cysteine, that ligates the [4Fe4S] cluster in a patient with colonic polyposis and family history of early age colon cancer. In bacterial MutY, the [4Fe4S] cluster is redox active, allowing rapid localization to target lesions by long-range, DNA-mediated signalling. In the current study, using DNA electrochemistry, we determine that wild-type MUTYH is similarly redox-active, but MUTYH C306W undergoes rapid oxidative degradation of its cluster to [3Fe4S]+, with loss of redox signalling. In MUTYH C306W, oxidative cluster degradation leads to decreased DNA binding and enzyme function. This study confirms redox activity in eukaryotic DNA repair proteins and establishes MUTYH C306W as a pathogenic variant, highlighting the essential role of redox signalling by the [4Fe4S] cluster.