期刊
SEMINARS IN CELL & DEVELOPMENTAL BIOLOGY
卷 30, 期 -, 页码 110-120出版社
ACADEMIC PRESS LTD- ELSEVIER SCIENCE LTD
DOI: 10.1016/j.semcdb.2014.04.014
关键词
Replication origins; Replication timing; Pre-replicative complex; Rif1; Chromatin loop
资金
- Grants-in-Aid for Scientific Research [23657081, 25650014] Funding Source: KAKEN
subset of the origins is actually fired to initiate DNA synthesis during S phase. Whereas factors involved in these steps are relatively well understood now, the mechanisms behind the origin specification, the choice of origins to be fired and determination of their timing are still under active investigation. Recent data show that the origin positions as well as the selection of those to be fired may be determined by multiple factors including sequences, chromatin context, epigenetic information, and some specific genomic features, but that the choice is surprisingly plastic and opportunistic. Timing regulation of firing, on the other hand, appears to be related to cell type-specific intrinsic chromatin architecture in nuclei. The conserved Rifl protein appears to be a major global regulator of the genome-wide replication timing. Replication timing is regulated also by other factors including checkpoint signals, local chromatin structures, timing and quantity of pre-RC formation, and availability of limiting initiation factors.(C) 2014 Elsevier Ltd. All rights reserved.
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