| Literature DB >> 33833428 |
Akihisa Osakabe1,2, Bhagyshree Jamge1, Elin Axelsson1, Sean A Montgomery1, Svetlana Akimcheva1, Annika Luisa Kuehn1,3, Rahul Pisupati1, Zdravko J Lorković1, Ramesh Yelagandula1,4, Tetsuji Kakutani5,6,2, Frédéric Berger7.
Abstract
Mobile transposable elements (TEs) not only participate in genome evolution but also threaten genome integrity. In healthy cells, TEs that encode all of the components that are necessary for their mobility are specifically silenced, yet the precise mechanism remains unknown. Here, we characterize the mechanism used by a conserved class of chromatin remodelers that prevent TE mobility. In the Arabidopsis chromatin remodeler DECREASE IN DNA METHYLATION 1 (DDM1), we identify two conserved binding domains for the histone variant H2A.W, which marks plant heterochromatin. DDM1 is necessary and sufficient for the deposition of H2A.W onto potentially mobile TEs, yet does not act on TE fragments or host protein-coding genes. DDM1-mediated H2A.W deposition changes the properties of chromatin, resulting in the silencing of TEs and, therefore, prevents their mobility. This distinct mechanism provides insights into the interplay between TEs and their host in the contexts of evolution and disease, and potentiates innovative strategies for targeted gene silencing.Entities:
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Year: 2021 PMID: 33833428 DOI: 10.1038/s41556-021-00658-1
Source DB: PubMed Journal: Nat Cell Biol ISSN: 1465-7392 Impact factor: 28.824