Impaired suppressive activities of human MUTYH variant proteins against oxidative mutagenesis

Kazuya Shinmura1, Masanori Goto, Hong Tao

  • 1Department of Tumor Pathology, Hamamatsu University School of Medicine, Shizuoka 431-3192, Japan. kzshinmu@hama-med.ac.jp

Abstract

Insights

MUTYH variant proteins, linked to colorectal cancer, show impaired activity against 8-hydroxyguanine (8OHG) DNA damage. These variants failed to suppress mutations caused by 8OHG in human cells, unlike wild-type MUTYH.

Area of Science:

  • Genetics
  • Molecular Biology
  • DNA Repair

Background:

  • MUTYH is a DNA glycosylase crucial for repairing oxidative DNA damage, specifically 8-hydroxyguanine (8OHG).
  • Mutations in MUTYH are associated with colorectal polyposis and cancer, suggesting a role in maintaining genomic stability.
  • Specific MUTYH variants (p.R154H, p.M255V, p.L360P, p.P377L) have been identified in patients but their functional impact on 8OHG repair remains unclear.

Purpose of the Study:

  • To investigate the functional suppressive activity of four specific MUTYH variant proteins against 8-hydroxyguanine (8OHG)-induced mutations in human cells.
  • To compare the DNA repair efficiency of these MUTYH variants with wild-type (WT) MUTYH in the context of oxidative DNA damage.

Main Methods:

  • Established human H1299 cancer cell lines inducibly expressing WT MUTYH or one of four MUTYH variants (p.R154H, p.M255V, p.L360P, p.P377L) using the piggyBac transposon system.
  • Confirmed MUTYH expression and nuclear localization via Western blotting and immunofluorescence.
  • Assessed the mutation frequency in a supF shuttle plasmid containing 8OHG using a supF forward mutation assay to evaluate DNA repair capacity.

Main Results:

  • All tested MUTYH variants and WT MUTYH localized to the nucleus, indicating proper cellular compartmentalization.
  • WT MUTYH significantly suppressed 8OHG-induced mutations compared to empty vector controls.
  • Conversely, the MUTYH variants (p.R154H, p.M255V, p.L360P, p.P377L) showed no significant suppressive activity against 8OHG-induced mutations, similar to empty vector cells.

Conclusions:

  • The MUTYH variants p.R154H, p.M255V, p.L360P, and p.P377L exhibit severely impaired suppressive activity against 8-hydroxyguanine-induced DNA mutations in human cells.
  • These findings suggest that the loss of functional repair of oxidative DNA damage by these MUTYH variants may contribute to the development of colorectal polyposis and cancer observed in patients.

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