A silencing pathway to induce H3-K9 and H4-K20 trimethylation at constitutive heterochromatin
Research Institute of Molecular Pathology · Vienna Biocenter · +2 more institutions
Abstract
Histone lysine methylation is a central modification to mark functionally distinct chromatin regions. In particular, H3-K9 trimethylation has emerged as a hallmark of pericentric heterochromatin in mammals. Here we show that H4-K20 trimethylation is also focally enriched at pericentric heterochromatin. Intriguingly, H3-K9 trimethylation by the Suv39h HMTases is required for the induction of H4-K20 trimethylation, although the H4 Lys 20 position is not an intrinsic substrate for these enzymes. By using a candidate approach, we identified Suv4-20h1 and Suv4-20h2 as two novel SET domain HMTases that localize to pericentric heterochromatin and specifically act as nucleosomal H4-K20 trimethylating enzymes.…
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Authors
8- GSGunnar Schotta
Research Institute of Molecular Pathology, Vienna Biocenter
- MLMonika Lachner
Research Institute of Molecular Pathology, Vienna Biocenter
- KSKavitha Sarma
Howard Hughes Medical Institute, Vienna Biocenter
- AEAnja Ebert
Vienna Biocenter, Martin Luther University Halle-Wittenberg
- RSRoopsha Sengupta
Research Institute of Molecular Pathology, Vienna Biocenter
Topics & keywords
- Biology
- Histone H3
- Heterochromatin
- EZH2
- Gene silencing
- Heterochromatin protein 1
- Genetics
- Molecular biology