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| Content Provider | Springer Nature Link |
|---|---|
| Author | Pope, Benjamin D. Hiratani, Ichiro Gilbert, David M. |
| Copyright Year | 2009 |
| Abstract | Studies of replication timing provide a handle into previously impenetrable higher-order levels of chromosome organization and their plasticity during development. Although mechanisms regulating replication timing are not clear, novel genome-wide studies provide a thorough survey of the extent to which replication timing is regulated during most of the early cell fate transitions in mammals, revealing coordinated changes of a defined set of 400–800 kb chromosomal segments that involve at least half the genome. Furthermore, changes in replication time are linked to changes in sub-nuclear organization and domain-wide transcriptional potential, and tissue-specific replication timing profiles are conserved from mouse to human, suggesting that the program has developmental significance. Hence, these studies have provided a solid foundation for linking megabase level chromosome structure to function, and suggest a central role for replication in domain-level genome organization. |
| Starting Page | 127 |
| Ending Page | 136 |
| Page Count | 10 |
| File Format | |
| ISSN | 09673849 |
| Journal | Chromosome Research |
| Volume Number | 18 |
| Issue Number | 1 |
| e-ISSN | 15736849 |
| Language | English |
| Publisher | Springer Netherlands |
| Publisher Date | 2009-12-15 |
| Publisher Place | Dordrecht |
| Access Restriction | One Nation One Subscription (ONOS) |
| Subject Keyword | Replication Timing Mammalian Development Cell Differentiation Chromosome Domains Nuclear Organization Chromatin Structure Sub-nuclear Positioning Transcriptional Competence Plant Genetics & Genomics Animal Genetics and Genomics Human Genetics Cell Biology |
| Content Type | Text |
| Resource Type | Article |
| Subject | Genetics |
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