4.8 Article

DNA damage response inhibition at dysfunctional telomeres by modulation of telomeric DNA damage response RNAs

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NATURE COMMUNICATIONS
卷 8, 期 -, 页码 -

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NATURE PUBLISHING GROUP
DOI: 10.1038/ncomms13980

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资金

  1. Fondazione Italiana per la Ricerca sul Cancro (FIRC) [12476]
  2. Marie Curie Initial Training Networks (FP7 PEOPLE ITN) [316354]
  3. European Union [600399]
  4. Associazione Italiana per la Ricerca sul Cancro, AIRC [12971]
  5. Human Frontier Science Program [RGP 0014/2012]
  6. Fondazione Telethon [GGP12059]
  7. European Research Council [322726]
  8. Japanese Ministry of Education, Culture, Sports, Science and Technology (MEXT)
  9. European Research Council (ERC) [322726] Funding Source: European Research Council (ERC)

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The DNA damage response (DDR) is a set of cellular events that follows the generation of DNA damage. Recently, site-specific small non-coding RNAs, also termed DNA damage response RNAs (DDRNAs), have been shown to play a role in DDR signalling and DNA repair. Dysfunctional telomeres activate DDR in ageing, cancer and an increasing number of identified pathological conditions. Here we show that, in mammals, telomere dysfunction induces the transcription of telomeric DDRNAs (tDDRNAs) and their longer precursors from both DNA strands. DDR activation and maintenance at telomeres depend on the biogenesis and functions of tDDRNAs. Their functional inhibition by sequence-specific antisense oligonucleotides allows the unprecedented telomere-specific DDR inactivation in cultured cells and in vivo in mouse tissues. In summary, these results demonstrate that tDDRNAs are induced at dysfunctional telomeres and are necessary for DDR activation and they validate the viability of locus-specific DDR inhibition by targeting DDRNAs.

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