4.7 Article

The chromatin remodelling factor ATRX suppresses R-loops in transcribed telomeric repeats

期刊

EMBO REPORTS
卷 18, 期 6, 页码 914-928

出版社

WILEY
DOI: 10.15252/embr.201643078

关键词

ATRX; G-quadruplex; R-loops; telomeres

资金

  1. MRC HIU
  2. MRC MHU [MC_UU_12009]
  3. NIHR Oxford BRC
  4. John Fell Fund [131/030, 101/517]
  5. EPA fund [CF182, CF170]
  6. WIMM Strategic Alliance [G0902418, MC_UU_12025]
  7. Marie Curie FP7 ITN DISCHROM
  8. Medical Research Council [MC_UU_12025/unit programme MC_UU_12009/3]
  9. Medical Research Council [MC_UU_00016/3, MC_U137961147, G1000801, MC_UU_12009/1, MC_UU_12009/3] Funding Source: researchfish
  10. MRC [MC_UU_00016/3, G1000801, MC_UU_12009/3, MC_U137961147, MC_UU_12009/1] Funding Source: UKRI

向作者/读者索取更多资源

ATRX is a chromatin remodelling factor found at a wide range of tandemly repeated sequences including telomeres (TTAGGG)(n). ATRX mutations are found in nearly all tumours that maintain their telomeres via the alternative lengthening of telomere (ALT) pathway, and ATRX is known to suppress this pathway. Here, we show that recruitment of ATRX to telomeric repeats depends on repeat number, orientation and, critically, on repeat transcription. Importantly, the transcribed telomeric repeats form RNA-DNA hybrids (R-loops) whose abundance correlates with the recruitment of ATRX. Here, we show loss of ATRX is also associated with increased R-loop formation. Our data suggest that the presence of ATRX at telomeres may have a central role in suppressing deleterious DNA secondary structures that form at transcribed telomeric repeats, and this may account for the increased DNA damage, stalling of replication and homology-directed repair previously observed upon loss of ATRX function.

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