| Literature DB >> 26012739 |
Dennis Sadic1, Katharina Schmidt1, Sophia Groh1, Ivan Kondofersky2, Joachim Ellwart3, Christiane Fuchs2, Fabian J Theis2, Gunnar Schotta4.
Abstract
More than 50% of mammalian genomes consist of retrotransposon sequences. Silencing of retrotransposons by heterochromatin is essential to ensure genomic stability and transcriptional integrity. Here, we identified a short sequence element in intracisternal A particle (IAP) retrotransposons that is sufficient to trigger heterochromatin formation. We used this sequence in a genome-wide shRNA screen and identified the chromatin remodeler Atrx as a novel regulator of IAP silencing. Atrx binds to IAP elements and is necessary for efficient heterochromatin formation. In addition, Atrx facilitates a robust and largely inaccessible heterochromatin structure as Atrx knockout cells display increased chromatin accessibility at retrotransposons and non-repetitive heterochromatic loci. In summary, we demonstrate a direct role of Atrx in the establishment and robust maintenance of heterochromatin.Entities:
Keywords: Atrx; Daxx; IAP retrotransposons; heterochromatin; histone H3.3
Mesh:
Substances:
Year: 2015 PMID: 26012739 PMCID: PMC4515123 DOI: 10.15252/embr.201439937
Source DB: PubMed Journal: EMBO Rep ISSN: 1469-221X Impact factor: 8.807