4.7 Article

Human RAP1 specifically protects telomeres of senescent cells from DNA damage

期刊

EMBO REPORTS
卷 21, 期 4, 页码 -

出版社

WILEY
DOI: 10.15252/embr.201949076

关键词

chromosome fusions; non-homologous end joining; RAP1; replicative senescence; telomeres

资金

  1. FEDER
  2. ARC
  3. Minitere de l'Enseignement Superieur
  4. region Provence Alpes-Cote d'Azur
  5. Inserm
  6. PHC Cai Yuanpei program of the Ministry of Foreign Affair
  7. Fondation ARC (Programme Labellise)
  8. Investments for the Future LABEX SIGNALIFE [ANR-11-LABX-0028-01]
  9. FRM [FDT20170437327]
  10. cross-cutting program of Inserm on aging (AGEMED)
  11. National Natural Science Foundation of China [81522017, 81971312, 91749126]
  12. Shanghai Municipal Education Commission (Oriental Scholars Program)
  13. Shanghai Municipal Science and Technology Commission [19XD1422500]
  14. Foundation of Shanghai Jiaotong University School of Medicine for Translational Medicine Innovation Project [15ZH4005]
  15. ANR (program TELOCHROM) Institut Nationale du Cancer (INCa) (program REPLITOP)
  16. MRC [G0500336] Funding Source: UKRI

向作者/读者索取更多资源

Repressor/activator protein 1 (RAP1) is a highly evolutionarily conserved protein found at telomeres. Although yeast Rap1 is a key telomere capping protein preventing non-homologous end joining (NHEJ) and consequently telomere fusions, its role at mammalian telomeres in vivo is still controversial. Here, we demonstrate that RAP1 is required to protect telomeres in replicative senescent human cells. Downregulation of RAP1 in these cells, but not in young or dividing pre-senescent cells, leads to telomere uncapping and fusions. The anti-fusion effect of RAP1 was further explored in a HeLa cell line where RAP1 expression was depleted through an inducible CRISPR/Cas9 strategy. Depletion of RAP1 in these cells gives rise to telomere fusions only when telomerase is inhibited. We further show that the fusions triggered by RAP1 loss are dependent upon DNA ligase IV. We conclude that human RAP1 is specifically involved in protecting critically short telomeres. This has important implications for the functions of telomeres in senescent cells.

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