期刊
DNA REPAIR
卷 11, 期 2, 页码 139-145出版社
ELSEVIER
DOI: 10.1016/j.dnarep.2011.10.013
关键词
Deinococcus radiodurans; PprI; Response regulator; DNA damage; Ionizing radiation
资金
- National Natural Science Foundation of China [30830006, 31000045]
- major scientific and technological project for significant new drugs creation [2009ZXJ09001-034]
- Special Fund for Agroscientific Research in the Public Interest [201103007]
- China Postdoctoral Science Foundation [20090460101, 201003728]
The extremely radioresistant bacterium Deinococcus radiodurans possesses a rapid and efficient but poorly known DNA damage response mechanism that mobilizes one-third of its genome to survive lethal radiation damage. Deinococcal PprI serves as a general switch to regulate the expression of dozens of proteins from different pathways after radiation, including the DNA repair proteins RecA, PprA and SSB. However, the underlying mechanism is poorly understood. In this study, we analyzed the dynamic alteration in global transcriptional profiles in wildtype and pprI mutant strains by combining microarrays and time-course sampling. We found that PprI up-regulated transcription of at least 210 genes after radiation, including 21 DNA repair and replication-related genes. We purified PprI and a helix-turn-helix (HTH) domain mutant and found that PprI specifically bound to the promoters of recA and pprA in vitro but did not bind nonspecific double-strand DNA. Chromatin immunoprecipitation (ChIP) assays confirmed that PprI specifically interacted with the promoter DNA of recA and pprA after radiation. Finally, we showed that a DNA-binding activity-deficient pprI mutant only partially restored resistance of the pprI mutant strain to gamma radiation, UV radiation, and mitomycin C. Taken together, these results indicate that DNA-binding activity is essential for PprI to program the DNA repair process and cellular survival of D. radiodurans in response to radiation damage. (C) 2011 Elsevier B.V. All rights reserved.
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