Abstract
MRX, an evolutionally conserved DNA damage response complex composed of Mre11, Rad50 and Xrs2, is involved in DNA double strand break (DSB) repair, checkpoint activation and telomere maintenance. At DSBs, MRX plays a role in generating single stranded DNA (ssDNA) and signalling cell cycle arrest. Here we investigated whether MRX also contributes to generating ssDNA or signalling cell cycle arrest at uncapped telomeres. To investigate the role of MRX, we generated a conditionally degradable Rad50 protein and combined this with cdc13-1, a temperature sensitive mutation in the Cdc13 telomere capping protein. We show that Rad50 does not contribute to ssDNA generation or cell cycle arrest in response to cdcl3-1 uncapped telomeres. Instead, we find that Rad50 inhibits ssDNA accumulation and promotes cdc13-1 cell viability, consistent with a major role for MRX in telomere capping.
Original language | English |
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Pages (from-to) | 840-851 |
Number of pages | 12 |
Journal | DNA Repair |
Volume | 5 |
Issue number | 7 |
Early online date | 12 Jun 2006 |
DOIs | |
Publication status | Published - 13 Jul 2006 |
Keywords
- RAD50
- MRX
- Telomere
- Checkpoint
- ssDNE
- CDC13
ASJC Scopus subject areas
- General Biochemistry,Genetics and Molecular Biology