Inherent asymmetry of Rpd3S coordinates its nucleosome engagement and association with elongating RNA polymerase II.
The Rpd3S histone deacetylase complex has a crucial role in genomic integrity by deacetylating transcribed nucleosomes following RNA polymerase (Pol)?II passage. Cryo-EM studies highlight the importance of asymmetrical Rco1-Eaf3 dimers in nucleosome binding, yet the interaction dynamics with nucleosomal substrates alongside elongating Pol?II are poorly understood. Here we demonstrate the ... essential function of the Rco1 N-terminal intrinsically disordered region (IDR) in modulating Pol?II association, in which K/R mutations within the Rco1 IDR impair interaction of Rpd3S with the C-terminal domain (CTD) of Rpb1, without affecting nucleosome recognition or complex integrity. We also identify the Rco1-PHD1 and Eaf3-CHD domains as crucial for specific binding to Ser5-phosphorylated CTD. The Rco1 IDR alleviates autoinhibition from its C terminus, facilitating PHD1-CHD engagement with phosphorylated CTD. Furthermore, we reveal a conserved mechanism by which asymmetrical Rco1-Eaf3 dimers coordinate nucleosome engagement and Pol?II interaction, enhancing understanding of epigenetic complexes associated with transcriptional machinery.
Mesh Terms:
Cryoelectron Microscopy, Histone Deacetylases, Intrinsically Disordered Proteins, Models, Molecular, Mutation, Nucleosomes, Phosphorylation, Protein Binding, Protein Domains, RNA Polymerase II, Saccharomyces cerevisiae, Saccharomyces cerevisiae Proteins
Cryoelectron Microscopy, Histone Deacetylases, Intrinsically Disordered Proteins, Models, Molecular, Mutation, Nucleosomes, Phosphorylation, Protein Binding, Protein Domains, RNA Polymerase II, Saccharomyces cerevisiae, Saccharomyces cerevisiae Proteins
Nat Struct Mol Biol
Date: Apr. 01, 2025
PubMed ID: 39779918
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