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Daujat, S.* ; Weiss, T.* ; Mohn, F.* ; Lange, U.C.* ; Ziegler-Birling, C.* ; Zeissler, U.* ; Lappe, M.* ; Schübeler, D.* ; Torres-Padilla, M.E.* ; Schneider, R.*

H3K64 trimethylation marks heterochromatin and is dynamically remodeled during developmental reprogramming.

Nat. Struct. Mol. Biol. 16, 777-781 (2009)
DOI PMC
Open Access Green as soon as Postprint is submitted to ZB.
Histone modifications are central to the regulation of all DNA-dependent processes. Lys64 of histone H3 (H3K64) lies within the globular domain at a structurally important position. We identify trimethylation of H3K64 (H3K64me3) as a modification that is enriched at pericentric heterochromatin and associated with repeat sequences and transcriptionally inactive genomic regions. We show that this new mark is dynamic during the two main epigenetic reprogramming events in mammals. In primordial germ cells, H3K64me3 is present at the time of specification, but it disappears transiently during reprogramming. In early mouse embryos, it is inherited exclusively maternally; subsequently, the modification is rapidly removed, suggesting an important role for H3K64me3 turnover in development. Taken together, our findings establish H3K64me3 as a previously uncharacterized histone modification that is preferentially localized to repressive chromatin. We hypothesize that H3K64me3 helps to 'secure' nucleosomes, and perhaps the surrounding chromatin, in an appropriately repressed state during development.
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Publication type Article: Journal article
Document type Scientific Article
Corresponding Author
ISSN (print) / ISBN 1545-9993
e-ISSN 1545-9985
Quellenangaben Volume: 16, Issue: 7, Pages: 777-781 Article Number: , Supplement: ,
Publisher Nature Publishing Group
Publishing Place New York, NY
Non-patent literature Publications
Reviewing status Peer reviewed