Developmental control of gene copy number by repression of replication initiation and fork progression
Author(s) -
Noa Sher,
George W. Bell,
Sharon Li,
Jared T. Nordman,
Thomas Eng,
Matthew L. Eaton,
David M. MacAlpine,
Terry L. OrrWeaver
Publication year - 2011
Publication title -
genome research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 9.556
H-Index - 297
eISSN - 1549-5469
pISSN - 1088-9051
DOI - 10.1101/gr.126003.111
Subject(s) - biology , pre replication complex , origin recognition complex , replication timing , dna replication factor cdt1 , genetics , dna replication , control of chromosome duplication , chromatin , minichromosome maintenance , replication factor c , polytene chromosome , licensing factor , eukaryotic dna replication , histone , gene , microbiology and biotechnology , drosophila melanogaster
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 is reinstated. Tethering of the SUUR protein to a specific site is insufficient to block replication, however. These results establish that developmental control of DNA replication, at both the initiation and elongation stages, is a mechanism to change gene copy number during differentiation.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom