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Updated: May 15, 2026

Isolating Potentiated Hsp104 Variants Using Yeast Proteinopathy Models
Published on: November 11, 2014
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
Aim:
To investigate the suppressive activity of MUTYH variant proteins against mutations caused by oxidative lesion, 8-hydroxyguanine (8OHG), in human cells.
Methods:
p.R154H, p.M255V, p.L360P, and p.P377L MUTYH variants, which were previously found in patients with colorectal polyposis and cancer, were selected for use in this study. Human H1299 cancer cell lines inducibly expressing wild-type (WT) MUTYH (type 2) or one of the 4 above-mentioned MUTYH variants were established using the piggyBac transposon vector system, enabling the genomic integration of the transposon sequence for MUTYH expression. MUTYH expression was examined after cumate induction using Western blotting analysis and immunofluorescence analysis. The intracellular localization of MUTYH variants tagged with FLAG was also immunofluorescently examined. Next, the mutation frequency in the supF of the shuttle plasmid pMY189 containing a single 8OHG residue at position 159 of the supF was compared between empty vector cells and cells expressing WT MUTYH or one of the 4 MUTYH variants using a supF forward mutation assay.
Results:
The successful establishment of human cell lines inducibly expressing WT MUTYH or one of the 4 MUTYH variants was concluded based on the detection of MUTYH expression in these cell lines after treatment with cumate. All of the MUTYH variants and WT MUTYH were localized in the nucleus, and nuclear localization was also observed for FLAG-tagged MUTYH. The mutation frequency of supF was 2.2 × 10(-2) in the 8OHG-containing pMY189 plasmid and 2.5 × 10(-4) in WT pMY189 in empty vector cells, which was an 86-fold increase with the introduction of 8OHG. The mutation frequency (4.7 × 10(-3)) of supF in the 8OHG-containing pMY189 plasmid in cells overexpressing WT MUTYH was significantly lower than in the empty vector cells (P < 0.01). However, the mutation frequencies of the supF in the 8OHG-containing pMY189 plasmid in cells overexpressing the p.R154H, p.M255V, p.L360P, or p.P377L MUTYH variant were 1.84 × 10(-2), 1.55 × 10(-2), 1.91 × 10(-2), and 1.96 × 10(-2), respectively, meaning that no significant difference was observed in the mutation frequency between the empty vector cells and cells overexpressing MUTYH mutants.
Conclusion:
The suppressive activities of p.R154H, p.M255V, p.L360P, and p.P377L MUTYH variants against mutations caused by 8OHG are thought to be severely impaired in human cells.
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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