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The Set1 N-terminal domain and Swd2 interact with RNA polymerase II CTD to recruit COMPASS.
- Source :
-
Nature communications [Nat Commun] 2020 May 01; Vol. 11 (1), pp. 2181. Date of Electronic Publication: 2020 May 01. - Publication Year :
- 2020
-
Abstract
- Methylation of histone H3 lysine 4 (H3K4) by Set1/COMPASS occurs co-transcriptionally, and is important for gene regulation. Set1/COMPASS associates with the RNA polymerase II C-terminal domain (CTD) to establish proper levels and distribution of H3K4 methylations. However, details of CTD association remain unclear. Here we report that the Set1 N-terminal region and the COMPASS subunit Swd2, which interact with each other, are both needed for efficient CTD binding in Saccharomyces cerevisiae. Moreover, a single point mutation in Swd2 that affects its interaction with Set1 also impairs COMPASS recruitment to chromatin and H3K4 methylation. A CTD interaction domain (CID) from the protein Nrd1 can partially substitute for the Set1 N-terminal region to restore CTD interactions and histone methylation. However, even when Set1/COMPASS is recruited via the Nrd1 CID, histone H2B ubiquitylation is still required for efficient H3K4 methylation, indicating that H2Bub acts after the initial recruitment of COMPASS to chromatin.
- Subjects :
- Chromatin Immunoprecipitation Sequencing
Histone-Lysine N-Methyltransferase genetics
Histones chemistry
Histones metabolism
Lysine metabolism
Methylation
Point Mutation
Protein Binding
Protein Domains
Protein Processing, Post-Translational
RNA Polymerase II genetics
RNA-Binding Proteins genetics
RNA-Binding Proteins metabolism
Saccharomyces cerevisiae genetics
Saccharomyces cerevisiae Proteins genetics
Ubiquitination
Chromatin metabolism
Histone-Lysine N-Methyltransferase metabolism
RNA Polymerase II metabolism
Saccharomyces cerevisiae metabolism
Saccharomyces cerevisiae Proteins metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 2041-1723
- Volume :
- 11
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- Nature communications
- Publication Type :
- Academic Journal
- Accession number :
- 32358498
- Full Text :
- https://doi.org/10.1038/s41467-020-16082-2