| Literature DB >> 28487353 |
Diu Tt Nguyen1, Hsiao Phin J Voon1,2, Barbara Xella1, Caroline Scott1, David Clynes1, Christian Babbs1, Helena Ayyub1, Jon Kerry1, Jacqueline A Sharpe1, Jackie A Sloane-Stanley1, Sue Butler1, Chris A Fisher1, Nicki E Gray3, Thomas Jenuwein4, Douglas R Higgs1, Richard J Gibbons5.
Abstract
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.Entities:
Keywords: zzm321990ATRXzzm321990; G‐quadruplex; R‐loops; telomeres
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Year: 2017 PMID: 28487353 PMCID: PMC5452009 DOI: 10.15252/embr.201643078
Source DB: PubMed Journal: EMBO Rep ISSN: 1469-221X Impact factor: 8.807