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| Content Provider | PubMed Central |
|---|---|
| Author | Sengupta, Sagar Robles, Ana I. Linke, Steven P. Sinogeeva, Natasha I. Zhang, Ran Remy, Pedeux Ward, Irene M. Celeste, Arkady André, Nussenzweig Chen, Junjie Halazonetis, Thanos D. Harris, Curtis C. |
| Abstract | Bloom's syndrome is a rare autosomal recessive genetic disorder characterized by chromosomal aberrations, genetic instability, and cancer predisposition, all of which may be the result of abnormal signal transduction during DNA damage recognition. Here, we show that BLM is an intermediate responder to stalled DNA replication forks. BLM colocalized and physically interacted with the DNA damage response proteins 53BP1 and H2AX. Although BLM facilitated physical interaction between p53 and 53BP1, 53BP1 was required for efficient accumulation of both BLM and p53 at the sites of stalled replication. The accumulation of BLM/53BP1 foci and the physical interaction between them was independent of γ-H2AX. The active Chk1 kinase was essential for both the accurate focal colocalization of 53BP1 with BLM and the consequent stabilization of BLM. Once the ATR/Chk1- and 53BP1-mediated signal from replicational stress is received, BLM functions in multiple downstream repair processes, thereby fulfilling its role as a caretaker tumor suppressor. |
| Related Links | http://dx.doi.org/10.1083/jcb.200405128 |
| Ending Page | 813 |
| Page Count | 13 |
| Starting Page | 801 |
| File Format | |
| ISSN | 00219525 |
| e-ISSN | 15408140 |
| Journal | The Journal of Cell Biology |
| Issue Number | 6 |
| Volume Number | 166 |
| Language | English |
| Publisher | The Rockefeller University Press |
| Publisher Date | 2004-09-13 |
| Access Restriction | Open |
| Rights Holder | The Rockefeller University Press |
| Subject Keyword | Cell Biology Research in Higher Education |
| Content Type | Text |
| Resource Type | Article |
| Subject | Cell Biology Medicine |
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