Molecular basis for the discrimination of repressive methyl-lysine marks in histone H3 by Polycomb and HP1 chromodomains
University of Virginia Health System · Pennsylvania State University · +4 more institutions
Abstract
On the histone H3 tail, Lys 9 and Lys 27 are both methylation sites associated with epigenetic repression, and reside within a highly related sequence motif ARKS. Here we show that the chromodomain proteins Polycomb (Pc) and HP1 (heterochromatin protein 1) are highly discriminatory for binding to these sites in vivo and in vitro. In Drosophila S2 cells, and on polytene chromosomes, methyl-Lys 27 and Pc are both excluded from areas that are enriched in methyl-Lys 9 and HP1. Swapping of the chromodomain regions of Pc and HP1 is sufficient for switching the nuclear localization patterns of these factors, indicating a role for their chromodomains in both target site binding and discrimination. To better understand…
Citation impact
- FWCI
- —
- Percentile
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- References
- 50
Authors
6- WFWolfgang FischleCorresponding
University of Virginia Health System
- YWYanming Wang
Pennsylvania State University, University of Virginia Health System, Cancer Institute (WIA), Rockefeller University
- SJSteven Jacobs
University of Virginia Health System, University of Virginia
- YKYoungchang Kim
Argonne National Laboratory
- CDC. David Allis
University of Virginia Health System, University of Virginia, Rockefeller University
Topics & keywords
- Chromodomain
- Heterochromatin protein 1
- Biology
- Histone H3
- Histone
- Heterochromatin
- Chromatin
- Methylation
- Reduced inequalities