AI Article Synopsis

  • MTH1 protein helps prevent the incorporation of damaged guanine (8-oxoguanine) into RNA by breaking down a specific nucleotide (8-oxoGTP).
  • During a study on aging mice, researchers found that older SAMP8 mice had higher levels of 8-oxoguanine in their RNA and lower MTH1 expression compared to younger or control mice.
  • Similar patterns of MTH1 deficiency and increased 8-oxoguanine were observed in the brains of Alzheimer's patients, suggesting that low MTH1 activity may contribute to aging and age-related diseases.

Article Abstract

Mammalian MTH1 protein, a MutT-related protein, catalyzes the hydrolysis of 8-oxo-7,8-dihydroguanosine triphosphate (8-oxoGTP) to monophosphate, thereby preventing incorporation of 8-oxo-7,8-dihydroguanine (8-oxoguanine) into RNA. In this study, we applied immunohistochemistry to follow the expression of MTH1 and the amount of 8-oxoguanine in RNA during aging. There were increased amounts of 8-oxoguanine in RNA in the CAl and CA3 subregions of hippocampi of 8- and 12-month-old SAMP8 mice, which exhibited early aging syndromes and declining learning and memory abilities compared to those of age-matched control SAMR1 mice. The expression levels of MTH1 in the hippocampi of 8- and 12-month-old SAMP8 mice were significantly lower than those of control mice. Therefore, in this mouse model, age-related accumulation of 8-oxoguanine in RNA is correlated with decreased expression of MTH1. Increased amounts of 8-oxoguanine in the RNA, and decreased expression of MTH1 were also observed in the hippocampi of patients suffering from Alzheimer's disease. These results suggest that MTH1 deficiency might be a causative factor for aging and age-related disorders.

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Source
http://dx.doi.org/10.1007/s11064-011-0484-4DOI Listing

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