期刊
JOURNAL OF CELL BIOLOGY
卷 193, 期 1, 页码 97-108出版社
ROCKEFELLER UNIV PRESS
DOI: 10.1083/jcb.201011083
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资金
- University of Cambridge
- CRUK [C6/A11224, C6/A11221]
- European Community (GENICA)
- CRUK
- Wellcome Trust
- EU [LSHG-CT-2005-512113]
- Biotechnology and Biological Sciences Research Council
- Cancer Research UK [11224] Funding Source: researchfish
Chromosomal deletions and rearrangements in tumors are often associated with common fragile sites, which are specific genomic loci prone to gaps and breaks in metaphase chromosomes. Common fragile sites appear to arise through incomplete DNA replication because they are induced after partial replication inhibition by agents such as aphidicolin. Here, we show that in G1 cells, large nuclear bodies arise that contain p53 binding protein 1 (53BP1), phosphorylated H2AX (gamma H2AX), and mediator of DNA damage checkpoint 1 (MDC1), as well as components of previously characterized OPT (Oct-1, PTF, transcription) domains. Notably, we find that incubating cells with low aphidicolin doses increases the incidence and number of 53BP1-OPT domains in G1 cells, and by chromatin immunoprecipitation and massively parallel sequencing analysis of gamma H2AX, we demonstrate that OPT domains are enriched at common fragile sites. These findings invoke a model wherein incomplete DNA synthesis during S phase leads to a DNA damage response and formation of 53BP1-OPT domains in the subsequent G1.
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