Epigenetic maintenance of PRC2-repressed chromatin requires RTT109 but not H3K56 acetylation
In animals, plants, and some fungi, Polycomb Repressive Complex 2 (PRC2) catalyzes trimethylation of histone H3 lysine 27 (H3K27me3) to establish transcriptionally repressed chromatin. Here, we identify the histone acetyltransferase RTT109 as a key regulator of PRC2-repressed domains in the model fungus Neurospora crassa . Although RTT109 interacts with the Vps75 homolog Nucleosome Assembly Factor 2 (NAF-2), we show that proper structure and function of PRC2-methylated chromatin require RTT109 catalytic activity but are independent of NAF-2 and H3K56 acetylation. We further demonstrate that H3K27me3 can be stably propagated over multiple rounds of mitosis in the absence of sequence-specific PRC2 targeting, and that RTT109 is essential for maintenance of the repressed state. These findings uncover a replication-linked mechanism for epigenetic memory and establish RTT109 as a key regulator of Polycomb-mediated chromatin inheritance.
Authors
- Rochelle E. Yap (ORCID: https://orcid.org/0000-0002-9181-280X)
- Felicia Ebot-Ojong (ORCID: https://orcid.org/0000-0002-3408-3487)
- Zachary Lewis (ORCID: https://orcid.org/0000-0002-1735-8266)
- Abigail J. Ameri
Institutions
- University of Georgia (US)
Publication Details
- Journal
- PLoS Genetics
- Published
- 2026-10-05
- DOI
- https://doi.org/10.1371/journal.pgen.1012327
- Primary Topic
- Epigenetics and DNA Methylation
- Type
- article
- Field-Weighted Citation Impact
- 0.00