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The chromatin remodeller ATRX facilitates diverse nuclear processes, in a stochastic manner, in both heterochromatin and euchromatin

Author

Listed:
  • Julia Truch

    (University of Oxford)

  • Damien J. Downes

    (University of Oxford)

  • Caroline Scott

    (University of Oxford)

  • E. Ravza Gür

    (University of Oxford
    University of Oxford)

  • Jelena M. Telenius

    (University of Oxford
    University of Oxford)

  • Emmanouela Repapi

    (University of Oxford)

  • Ron Schwessinger

    (University of Oxford
    University of Oxford)

  • Matthew Gosden

    (University of Oxford)

  • Jill M. Brown

    (University of Oxford)

  • Stephen Taylor

    (University of Oxford)

  • Pak Leng Cheong

    (University of Oxford)

  • Jim R. Hughes

    (University of Oxford
    University of Oxford)

  • Douglas R. Higgs

    (University of Oxford)

  • Richard J. Gibbons

    (University of Oxford)

Abstract

The chromatin remodeller ATRX interacts with the histone chaperone DAXX to deposit the histone variant H3.3 at sites of nucleosome turnover. ATRX is known to bind repetitive, heterochromatic regions of the genome including telomeres, ribosomal DNA and pericentric repeats, many of which are putative G-quadruplex forming sequences (PQS). At these sites ATRX plays an ancillary role in a wide range of nuclear processes facilitating replication, chromatin modification and transcription. Here, using an improved protocol for chromatin immunoprecipitation, we show that ATRX also binds active regulatory elements in euchromatin. Mutations in ATRX lead to perturbation of gene expression associated with a reduction in chromatin accessibility, histone modification, transcription factor binding and deposition of H3.3 at the sequences to which it normally binds. In erythroid cells where downregulation of α-globin expression is a hallmark of ATR-X syndrome, perturbation of chromatin accessibility and gene expression occurs in only a subset of cells. The stochastic nature of this process suggests that ATRX acts as a general facilitator of cell specific transcriptional and epigenetic programmes, both in heterochromatin and euchromatin.

Suggested Citation

  • Julia Truch & Damien J. Downes & Caroline Scott & E. Ravza Gür & Jelena M. Telenius & Emmanouela Repapi & Ron Schwessinger & Matthew Gosden & Jill M. Brown & Stephen Taylor & Pak Leng Cheong & Jim R. , 2022. "The chromatin remodeller ATRX facilitates diverse nuclear processes, in a stochastic manner, in both heterochromatin and euchromatin," Nature Communications, Nature, vol. 13(1), pages 1-16, December.
  • Handle: RePEc:nat:natcom:v:13:y:2022:i:1:d:10.1038_s41467-022-31194-7
    DOI: 10.1038/s41467-022-31194-7
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    References listed on IDEAS

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    1. Jason Ernst & Pouya Kheradpour & Tarjei S. Mikkelsen & Noam Shoresh & Lucas D. Ward & Charles B. Epstein & Xiaolan Zhang & Li Wang & Robbyn Issner & Michael Coyne & Manching Ku & Timothy Durham & Mano, 2011. "Mapping and analysis of chromatin state dynamics in nine human cell types," Nature, Nature, vol. 473(7345), pages 43-49, May.
    2. Carla Danussi & Promita Bose & Prasanna T. Parthasarathy & Pedro C. Silberman & John S. Van Arnam & Mark Vitucci & Oliver Y. Tang & Adriana Heguy & Yuxiang Wang & Timothy A. Chan & Gregory J. Riggins , 2018. "Atrx inactivation drives disease-defining phenotypes in glioma cells of origin through global epigenomic remodeling," Nature Communications, Nature, vol. 9(1), pages 1-15, December.
    3. David Clynes & Clare Jelinska & Barbara Xella & Helena Ayyub & Caroline Scott & Matthew Mitson & Stephen Taylor & Douglas R. Higgs & Richard J. Gibbons, 2015. "Suppression of the alternative lengthening of telomere pathway by the chromatin remodelling factor ATRX," Nature Communications, Nature, vol. 6(1), pages 1-11, November.
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    Cited by:

    1. Nitish Gulve & Chenhe Su & Zhong Deng & Samantha S. Soldan & Olga Vladimirova & Jayamanna Wickramasinghe & Hongwu Zheng & Andrew V. Kossenkov & Paul. M. Lieberman, 2022. "DAXX-ATRX regulation of p53 chromatin binding and DNA damage response," Nature Communications, Nature, vol. 13(1), pages 1-14, December.

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