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Formation of a Polycomb-Domain in the Absence of Strong Polycomb Response Elements.
- Source :
-
PLoS genetics [PLoS Genet] 2016 Jul 28; Vol. 12 (7), pp. e1006200. Date of Electronic Publication: 2016 Jul 28 (Print Publication: 2016). - Publication Year :
- 2016
-
Abstract
- Polycomb group response elements (PREs) in Drosophila are DNA-elements that recruit Polycomb proteins (PcG) to chromatin and regulate gene expression. PREs are easily recognizable in the Drosophila genome as strong peaks of PcG-protein binding over discrete DNA fragments; many small but statistically significant PcG peaks are also observed in PcG domains. Surprisingly, in vivo deletion of the four characterized strong PREs from the PcG regulated invected-engrailed (inv-en) gene complex did not disrupt the formation of the H3K27me3 domain and did not affect inv-en expression in embryos or larvae suggesting the presence of redundant PcG recruitment mechanism. Further, the 3D-structure of the inv-en domain was only minimally altered by the deletion of the strong PREs. A reporter construct containing a 7.5kb en fragment that contains three weak peaks but no large PcG peaks forms an H3K27me3 domain and is PcG-regulated. Our data suggests a model for the recruitment of PcG-complexes to Drosophila genes via interactions with multiple, weak PREs spread throughout an H3K27me3 domain.
- Subjects :
- Animals
DNA-Binding Proteins biosynthesis
Drosophila melanogaster genetics
Gene Expression Regulation, Developmental
Genome, Insect
Histone Demethylases genetics
Imaginal Discs growth & development
Imaginal Discs metabolism
Larva genetics
Larva growth & development
Polycomb-Group Proteins biosynthesis
Polycomb-Group Proteins chemistry
Protein Binding genetics
Protein Domains genetics
Chromatin genetics
DNA-Binding Proteins genetics
Polycomb-Group Proteins genetics
Response Elements genetics
Subjects
Details
- Language :
- English
- ISSN :
- 1553-7404
- Volume :
- 12
- Issue :
- 7
- Database :
- MEDLINE
- Journal :
- PLoS genetics
- Publication Type :
- Academic Journal
- Accession number :
- 27466807
- Full Text :
- https://doi.org/10.1371/journal.pgen.1006200