RAD51 localization and activation following DNA damage

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PARP-2 domain requirements for DNA damage-dependent activation and localization to sites of DNA damage.

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p53-Dependent subcellular proteome localization following DNA damage

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Single-molecule localization microscopy reveals molecular transactions during RAD51 filament assembly at cellular DNA damage sites

RAD51 recombinase assembles on single-stranded (ss)DNA substrates exposed by DNA end-resection to initiate homologous recombination (HR), a process fundamental to genome integrity. RAD51 assembly has been characterized using purified proteins, but its ultrastructural topography in the cell nucleus is unexplored. Here, we combine cell genetics with single-molecule localization microscopy and a p...

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Coordinated response of mammalian Rad51 and Rad52 to DNA damage.

Biochemical analysis has shown that mammalian Rad51 and Rad52 interact and synergize in DNA recombination reactions in vitro, but these proteins have not been shown to function together in response to DNA damage in vivo. By analysis of murine cells expressing murine Rad52 tagged with green fluorescent protein (GFP)-Rad52, we now show that DNA damage causes Rad51 and GFP-Rad52 to colocalize in d...

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Homologous recombination is essential for RAD51 up-regulation in Saccharomyces cerevisiae following DNA crosslinking damage.

We have determined the kinetics of up-regulation of the homologous recombination gene RAD51, one of the genes induced following DNA damage in isogenic haploid DNA repair-deficient mutants of Saccharomyces cerevisiae, using treatment with the DNA crosslinking agent 8-methoxypsoralen. We show that RAD51 is up-regulated concomitantly, although independently, with a shift from the G1 cell cycle pha...

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ژورنال

عنوان ژورنال: Philosophical Transactions of the Royal Society of London. Series B: Biological Sciences

سال: 2004

ISSN: 0962-8436,1471-2970

DOI: 10.1098/rstb.2003.1368