Interactions among Polycomb Domains Are Guided by Chromosome Architecture
Polycomb group (PcG) proteins bind and regulate hundreds of genes. Previous evidence has suggested that long-range chromatin interactions may contribute to the regulation of PcG target genes. Here, we adapted the Chromosome Conformation Capture on Chip (4C) assay to systematically map chromosomal in...
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| Published in: | PLoS genetics Vol. 7; no. 3; p. e1001343 |
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| Main Authors: | , , , , , , , , , |
| Format: | Journal Article |
| Language: | English |
| Published: |
United States
Public Library of Science
01.03.2011
Public Library of Science (PLoS) |
| Subjects: | |
| ISSN: | 1553-7404, 1553-7390, 1553-7404 |
| Online Access: | Get full text |
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| Summary: | Polycomb group (PcG) proteins bind and regulate hundreds of genes. Previous evidence has suggested that long-range chromatin interactions may contribute to the regulation of PcG target genes. Here, we adapted the Chromosome Conformation Capture on Chip (4C) assay to systematically map chromosomal interactions in Drosophila melanogaster larval brain tissue. Our results demonstrate that PcG target genes interact extensively with each other in nuclear space. These interactions are highly specific for PcG target genes, because non-target genes with either low or high expression show distinct interactions. Notably, interactions are mostly limited to genes on the same chromosome arm, and we demonstrate that a topological rather than a sequence-based mechanism is responsible for this constraint. Our results demonstrate that many interactions among PcG target genes exist and that these interactions are guided by overall chromosome architecture. |
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| Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 Conceived and designed the experiments: BT MvL BvS. Performed the experiments: BT MB HT. Analyzed the data: BT. Contributed reagents/materials/analysis tools: RMK LP HT MN MS WdL. Wrote the paper: BT MvL BvS. |
| ISSN: | 1553-7404 1553-7390 1553-7404 |
| DOI: | 10.1371/journal.pgen.1001343 |