RNA-dependent stabilization of SUV39H1 at constitutive heterochromatin

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Johnson, WL

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Yewdell, WT

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Bell, JC

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McNulty, SM

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Duda, Z

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O’Neill, RJ

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Sullivan, BA

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Straight, AF

dc.date.accessioned

2020-09-23T13:03:10Z

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2020-09-23T13:03:10Z

dc.date.issued

2017-08-01

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2020-09-23T13:03:09Z

dc.description.abstract

© Johnson et al. Heterochromatin formed by the SUV39 histone methyltransferases represses transcription from repetitive DNA sequences and ensures genomic stability. How SUV39 enzymes localize to their target genomic loci remains unclear. Here, we demonstrate that chromatin-associated RNA contributes to the stable association of SUV39H1 with constitutive heterochromatin in human cells. We find that RNA associated with mitotic chromosomes is concentrated at pericentric heterochromatin, and is encoded, in part, by repetitive a-satellite sequences, which are retained in cis at their transcription sites. Purified SUV39H1 directly binds nucleic acids through its chromodomain; and in cells, SUV39H1 associates with a-satellite RNA transcripts. Furthermore, nucleic acid binding mutants destabilize the association of SUV39H1 with chromatin in mitotic and interphase cells - effects that can be recapitulated by RNase treatment or RNA polymerase inhibition - and cause defects in heterochromatin function. Collectively, our findings uncover a previously unrealized function for chromatin-associated RNA in regulating constitutive heterochromatin in human cells.

dc.identifier.issn

2050-084X

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https://hdl.handle.net/10161/21536

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eLife Sciences Publications, Ltd

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eLife

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10.7554/eLife.25299.001

dc.title

RNA-dependent stabilization of SUV39H1 at constitutive heterochromatin

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Journal article

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Sullivan, BA|0000-0001-5216-4603

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School of Medicine

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Duke Cancer Institute

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Molecular Genetics and Microbiology

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Duke Science & Society

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Duke

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Institutes and Centers

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Basic Science Departments

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Initiatives

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Institutes and Provost's Academic Units

pubs.publication-status

Published

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6

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