4.8 Article

Transcription errors induce proteotoxic stress and shorten cellular lifespan

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NATURE COMMUNICATIONS
卷 6, 期 -, 页码 -

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NATURE PUBLISHING GROUP
DOI: 10.1038/ncomms9065

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资金

  1. NIH [GM092741, R01GM56981, R01AG039390, T32AG000057, T32ES007032]
  2. NIA [11006596]
  3. National Institutes of Health, National Cancer Institute
  4. Center for Cancer Research
  5. [R01 GM079480]
  6. [GM 080294]
  7. NATIONAL INSTITUTE OF ENVIRONMENTAL HEALTH SCIENCES [T32ES007032] Funding Source: NIH RePORTER
  8. NATIONAL INSTITUTE OF GENERAL MEDICAL SCIENCES [R01GM056981, R01GM092741, R01GM067785, R01GM079480, R01GM080294, T32GM008570] Funding Source: NIH RePORTER
  9. NATIONAL INSTITUTE ON AGING [T32AG000057, P30AG013280, R01AG039390] Funding Source: NIH RePORTER

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Transcription errors occur in all living cells; however, it is unknown how these errors affect cellular health. To answer this question, we monitor yeast cells that are genetically engineered to display error-prone transcription. We discover that these cells suffer from a profound loss in proteostasis, which sensitizes them to the expression of genes that are associated with protein-folding diseases in humans; thus, transcription errors represent a new molecular mechanism by which cells can acquire disease phenotypes. We further find that the error rate of transcription increases as cells age, suggesting that transcription errors affect proteostasis particularly in aging cells. Accordingly, transcription errors accelerate the aggregation of a peptide that is implicated in Alzheimer's disease, and shorten the lifespan of cells. These experiments reveal a previously unappreciated role for transcriptional fidelity in cellular health and aging.

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