Abstract
Dimethylation of histone H3 Arg2 (H3R2me2) maintains transcriptional silencing by inhibiting Set1 mediated trimethylation of H3K4. Here we demonstrate that Arg2 is also monomethylated (H3R2me1) in yeast but that its functional characteristics are distinct from H3R2me2: (i) H3R2me1 does not inhibit histone H3 Lys4 (H3K4) methylation; (ii) it is present throughout the coding region of genes; and (iii) it correlates with active transcription. Collectively, these results indicate that different H3R2 methylation states have defined roles in gene expression.
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Acknowledgements
We thank members of the T.K. laboratory for helpful discussions and M. Gilchrist for help with depositing genomic data. This work was supported by postdoctoral fellowship grants to A.K. from the European Molecular Biology Organization (EMBO) and Marie Curie. The T.K. laboratory is funded by grants from Cancer Research UK (CRUK) and the 6th Research Framework Program of the European Union (Epitron and Heroic).
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T.K. is a director of Abcam Plc. R.D.G. and M.A.S. are employees of NimbleGen Systems Inc.
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Kirmizis, A., Santos-Rosa, H., Penkett, C. et al. Distinct transcriptional outputs associated with mono- and dimethylated histone H3 arginine 2. Nat Struct Mol Biol 16, 449–451 (2009). https://doi.org/10.1038/nsmb.1569
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DOI: https://doi.org/10.1038/nsmb.1569
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