Developmental control of gene copy number by repression of replication initiation and fork progression
- Noa Sher1,
- George W. Bell1,
- Sharon Li1,
- Jared Nordman1,
- Thomas Eng2,
- Matthew L Eaton3,
- David M MacAlpine3 and
- Terry L Orr-Weaver2,4
- 1 Whitehead Institute for Biomedical Research;
- 2 Whitehead Institute for Biomedical Research, Dept. of Biology, Massachusetts Institute of Technology;
- 3 Dept. of Pharmacology and Cancer Biology, Duke University Medical Center
- ↵* Corresponding author; email: weaver{at}wi.mit.edu
Abstract
Precise DNA replication is crucial for genome maintenance, yet this process has been inherently difficult to study on a genome-wide level in untransformed differentiated metazoan cells. To determine how metazoan DNA replication can be repressed, we examined regions selectively under-replicated in Drosophila polytene salivary glands and found they are transcriptionally silent and enriched for the repressive H3K27me3 mark. In the first genome-wide analysis of binding of the Origin Recognition Complex (ORC) in a differentiated metazoan tissue, we find that ORC binding is dramatically reduced within these large domains, suggesting reduced initiation as one mechanism leading to under-replication. Inhibition of replication fork progression by the chromatin protein SUUR is an additional repression mechanism to reduce copy number. Although repressive histone marks are removed when SUUR is mutated and copy number restored, neither transcription nor ORC binding are reinstated. Tethering of SUUR protein to a specific site is insufficient to block replication, however. These results establish that developmental control of DNA replication, both at the initiation and elongation stages, is a mechanism to change gene copy number during differentiation.
- Received May 7, 2011.
- Accepted October 17, 2011.
- Copyright © 2011, Cold Spring Harbor Laboratory Press
This manuscript is Open Access.











