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PMID: 19143474 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Functional anatomy of polycomb and trithorax chromatin landscapes in Drosophila embryos.

PLoS biology ·Vol. 7 ·No. 1 ·2009-01-13 ·Pages e13

Schuettengruber B, Ganapathi M, Leblanc B, Portoso M, Jaschek R, Tolhuis B, van Lohuizen M, Tanay A, Cavalli G

Abstract

Polycomb group (PcG) and trithorax group (trxG) proteins are conserved chromatin factors that regulate key developmental genes throughout development. In Drosophila, PcG and trxG factors bind to regulatory DNA elements called PcG and trxG response elements (PREs and TREs). Several DNA binding proteins have been suggested to recruit PcG proteins to PREs, but the DNA sequences necessary and sufficient to define PREs are largely unknown. Here, we used chromatin immunoprecipitation (ChIP) on chip assays to map the chromosomal distribution of Drosophila PcG proteins, the N- and C-terminal fragments of the Trithorax (TRX) protein and four candidate DNA-binding factors for PcG recruitment. In addition, we mapped histone modifications associated with PcG-dependent silencing and TRX-mediated activation. PcG proteins colocalize in large regions that may be defined as polycomb domains and colocalize with recruiters to form several hundreds of putative PREs. Strikingly, the majority of PcG recruiter binding sites are associated with H3K4me3 and not with PcG binding, suggesting that recruiter proteins have a dual function in activation as well as silencing. One major discriminant between activation and silencing is the strong binding of Pleiohomeotic (PHO) to silenced regions, whereas its homolog Pleiohomeotic-like (PHOL) binds preferentially to active promoters. In addition, the C-terminal fragment of TRX (TRX-C) showed high affinity to PcG binding sites, whereas the N-terminal fragment (TRX-N) bound mainly to active promoter regions trimethylated on H3K4. Our results indicate that DNA binding proteins serve as platforms to assist PcG and trxG binding. Furthermore, several DNA sequence features discriminate between PcG- and TRX-N-bound regions, indicating that underlying DNA sequence contains critical information to drive PREs and TREs towards silencing or activation.

MeSH Terms
Animals Chromatin/physiology Chromatin Immunoprecipitation Chromosomal Proteins, Non-Histone/physiology Drosophila Proteins/physiology Drosophila melanogaster/embryology Gene Expression Regulation, Developmental/physiology Polycomb Repressive Complex 1 Reverse Transcriptase Polymerase Chain Reaction
Chemicals
Chromatin Chromosomal Proteins, Non-Histone Drosophila Proteins Pc protein, Drosophila trx protein, Drosophila Polycomb Repressive Complex 1
Authors & Affiliations
9 authors, click to expand affiliations / ORCID
Schuettengruber Bernd
Institut de Génétique Humaine, CNRS, Montpellier, France.
Ganapathi Mythily
Leblanc Benjamin
Portoso Manuela
Jaschek Rami
Tolhuis Bas
van Lohuizen Maarten
Tanay Amos
Cavalli Giacomo
Conflict of Interest

Competing interests. The authors have declared that no competing interests exist.

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Article Info
Journal
PLoS biology
Abbr.
PLoS Biol
ISSN
1545-7885
Published
2009-01-13
Pages
e13
Language
English
Region
United States
NLM ID
101183755
PMCID
PMC2621266
Subset
IM
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