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耐辐射球菌抗氧化相关调控子及紫外辐射后转录组的研究
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摘要
耐辐射球菌不仅对电离辐射具有惊人的抗性,而且对过氧化氢、紫外线和干燥以及其它物理化学诱变因子都具有极强的抗性。迄今为止,我们对它的极端抗性的分子机制了解的还很有限。研究证明电离辐射对DNA直接损伤为20%,80%DNA的损伤是由氧化压力间接产生的,说明了耐辐射球菌的抗氧化能力是其电离辐射抗性一个重要因素。活性氧应激子OxyR是一种广泛存在于细菌中的LysR型转录调节因子家族的成员,大肠杆菌OxyR能够感受过氧化氢胁迫并启动细胞的抗氧化系统。本文对耐辐射球菌中氧化相关的转录因子OxyR2(DRA0336)在抗氧化过程中的作用进行了一定的研究,有助于从另一个角度深入理解这极端抗性。本论文还利用基因芯片技术对紫外辐射后耐辐射球菌的全基因组表达进行了分析。
     1、首先生物信息学分析发现除了OxyR (DR0615)耐辐射球菌中可能存在E. coli OxyR的另一个同源物OxyR2 (DRA0336)。多序列比对表明涉及DNA结合结构域、蛋白四聚化、激活区域和形成疏水中心的多个关键氨基酸位点和一个重要的半光氨酸位点C208都是十分保守,这是第一次发现细菌中可能存在两个OxyR同源物。利用完全缺失突变的方法构建了oxyR2基因的单突变菌株、oxyR2和oxyR基因的双突变菌株DM,同时构建完整补偿株MOxyR2-MC和N端截短48个核苷酸的补偿株MOxyR2-CΔN,再利用定点突变法构建半胱氨酸定点突变的补偿株包括MOxyR2-MC228,MOxyR2-MC272和MOxyR2-MC290。
     2、对各个突变株和补偿株的特性进行分析,过氧化氢胁迫下的生存率分析表明oxyR2基因的敲除导致突变株对过氧化氢氧化胁迫很敏感,进一步分析表明突变株内的过氧化氢酶总活性降低以及ROS积累更多。双突变DM比单突变对过氧化氢处理更敏感,过氧化氢酶更低以及ROS积累更多。补偿实验表明耐辐射球菌的全基因以和N端截短48个核苷酸的oxyR2都能完全补偿其氧化抗性,但耐辐射球菌OxyR2不能补偿E coli的OxyR突变株GS09。半胱氨酸定点突变的补偿株分析表明OxyR2的C228是耐辐射球菌在氧化胁迫过程中存活的一个关键位点。QRT-PCR结果表明耐辐射球菌的oxyR和oxyR2是持续表达的而且彼此的突变株并不存在由于氧化胁迫而导致的转录补偿。这些实验结果说明oxyR2是耐辐射球菌抗氧化过程所必须的。
     3、利用耐辐射球菌全基因组的olig芯片分析了DRA0336突变株全基因组的转录水平,比较了突变株和野生株在20mM过氧化氢处理后转录水平差异。发现MOxyR2中共有103个基因改变了其表达模式,表现出ROS的应急反应:抗氧化相关基因,铁代谢相关基因以及容易产生ROS的相关基因受到明显抑制。
     4、用基因芯片技术从转录水平研究耐辐射球菌紫外辐射后全基因组的表达谱,耐辐射球菌在800J/m2紫外辐射后的总共有167个基因发生表达模式改变,其中87个基因表达上调和81个基因表达下调,DNA修复相关的基因uvsE, uvrA2, uvrB, uvrC, uvrD, recA和pprA都受到紫外辐射的诱导。同时芯片数据表明耐辐射在紫外辐射后没有表现出一个经典的SOS反应机制,而且DNA复制的起始因子dnaA和分裂有关因子minE的下调说明紫外辐射后可能存在一个停滞的修复期。
Deinococcus radiodurans is characterized by its extraordinary resistance to all kinds of DNA damaging agents, such as ionizing radiation, hydrogen peroxide, UV radiation, desiccation and other physical and chemical DNA damaging agents However, to date the molecular mechanism responsible for the astonishing resistance is not well understand. It has been demonstrated that damaging effects of ionizing radiation are due to the indirect oxidative stress to DNA. This indicates that the antioxidation ability is importantly contributed to the resistance to ionizing radiation. OxyR which belongs to the LysR family of transcriptional regulator widely exit in bacteria. E. coli OxyR regulates expression of the majority of genes response to hydrogen peroxide. In this study, the function of D. radiodurans OxyR2 (DRA0336) were investigated. In addition, the genome transcriptional profiling of D. radiodurans following 800 J/m2 UV radiation was studied. The results as below:
     1. Analysis of the D. radiodurans R1 genome using the BLAST program with the E. coli OxyR amino acid sequence as a query sequence revealed the presence of another putative homolog DRA0336 (OxyR2). Multiple amino acid sequence alignment indicated amino acid residues of OxyR2 involved in DNA binding domain, protein tetramerization, possible activating region and key cysteine residue C208 are conserved. It is first found that there exit two homologues in one bacterium. To investigate the function, we constructed the deletion mutant of oxyR2 and the double mutant of oxyR oxyR2/oxyR2. MOxyR2-C strains and MOxyR2-CΔN strains, complemented by full OxyR2 or OxyR2 with N terminal absence of 16 amino acids respectively, were also constructed. PCR site-direct mutagenesis was performed to construct MOxyR2-MC228, MOxyR2-MC272和MOxyR2-MC290 strains.
     2. All mutant strains and complementary strains were characterized. Survival rate assay with H2O2 treatment indicated that MOxyR2 was significantly more sensitive to H2O2 compared to the wild type. The complementation experiment showed that tans-expression of the OxyR2 or OxyR2 with N terminal absence of 16 amino acids in MOxyR2 could fully restore the H2O2 resistance. C228 is a crucial site for survival in H2O2 stress. The double mutant DM was significantly more sensitive to H2O2 than any of the single mutants. MOxyR2 accumulated much more ROS than the wild type R1 and DM accumulated the highest level of ROS. Deletion of oxyR2 attenuates the enzymatic activity of catalase and DM had almost no increase after the treatment with H2O2. These results demonstrate that the oxyR2 gene is responsible for the sensitivity to hydrogen peroxide.
     3. To test the role of OxyR2 in D. radiodurans under H2O2 treatment, the whole genome expression profile of MOxyR2 was performed in comparison with R1 after treatment with 20 mM H2O2 during the exponential growth phase. The result showed that total 103 genes changed the expression pattern and exhibited response to ROS emergency. One obvious character was that many genes related with production of ROS, antioxidation and iron metabolism significantly down-regulated.
     4. To better understand the response mechanism how D. radiodurans coped with the UV irradiation, the investigation of the global gene expression profile in response to UV irradiation was performed. Overall,167 of the total predicted D. radiodurans genes represented on the chip were pronouncedly differentially expressed following UV irradiation of 800 J/m2 after 30 min of post-irradiation incubation. DNA repair gene including uvsE, uvrA2, uvrB, uvrC, uvrD, pprA and recA were induced. The microarray results indicate that there may be no SOS response after UV radiation in D. radiodurans. DNA replication initiation factor dnaA and minE related with mitosis were obviously down-regulated. These indicated that there may exit a period of stasis characterized by repair phase.
引文
Anderson AW, Nordon HC, R.F.Cain, Parrish G & Duggan G (1956) Studies on a radio-resistant microccus. Ⅰ. Isolation, morphology, cultural characteristics, and resistance to gamma radiation. Food Technol 10:575-578:
    Anderson R & Hansen K (1985) Structure of a novel phosphoglycolipid from Deinococcus radiodurans. J Biol Chem 260:12219-12223.
    Aslund F, Zheng M, Beckwith J & Storz G (1999) Regulation of the OxyR transcription factor by hydrogen peroxide and the cellular thiol-disulfide status. Proc Natl Acad Sci U S A 96:6161-6165.
    Bentchikou E, Servant P, Coste G & Sommer S (2007) Additive effects of SbcCD and PoIX deficiencies in the in vivo repair of DNA double-strand breaks in Deinococcus radiodurans. J Bacteriol 189:4784-4790.
    Blasius M, Buob R, Shevelev Ⅳ & Hubscher U (2007) Enzymes involved in DNA ligation and end-healing in the radioresistant bacterium Deinococcus radiodurans. BMC Mol Biol 8:69.
    Brim H, McFarlan SC, Fredrickson JK, Minton KW, Zhai M, Wackett LP & Daly MJ (2000) Engineering Deinococcus radiodurans for metal remediation in radioactive mixed waste environments. Nat Biotechnol 18:85-90.
    Chen H, Xu G, Zhao Y, et al. (2008) A novel OxyR sensor and regulator of hydrogen peroxide stress with one cysteine residue in Deinococcus radiodurans. PLoS ONE 3:e1602.
    Chen H, Huang L, Hua X, et al. (2009) Pleiotropic effects of RecQ in Deinococcus radiodurans. Genomics 94:333-340.
    Choi H, Kim S, Mukhopadhyay P, Cho S, Woo J, Storz G & Ryu S (2001) Structural basis of the redox switch in the OxyR transcription factor. Cell 105: 103-113.
    Chou Fl & Tan ST (1990) Manganese(Ⅱ) induces cell division and increases in superoxide dismutase and catalase activities in an aging deinococcal culture. J Bacteriol 172:2029-2035.
    Christman MF, Storz G & Ames BN (1989) OxyR, a positive regulator of hydrogen peroxide-inducible genes in Escherichia coli and Salmonella typhimurium, is homologous to a family of bacterial regulatory proteins. Proc Natl Acad Sci U S A 86:3484-3488.
    Christman MF, Morgan RW, Jacobson FS & Ames BN (1985) Positive control of a regulon for defenses against oxidative stress and some heat-shock proteins in Salmonella typhimurium. Cell 41:753-762.
    Cuypers MG, Mitchell EP, Romao CV & McSweeney SM (2007) The Crystal Structure of the Dps2 from Deinococcus radiodurans Reveals an Unusual Pore Profile with a Non-specific Metal Bindigng Site. J Mol Biol 371:787-799.
    Daly MJ (2009) A new perspective on radiation resistance based on Deinococcus radiodurans. Nat Rev Microbiol 7:237-245.
    Daly MJ & Minton KW (1996) An alternative pathway of recombination of chromosomal fragments precedes recA-dependent recombination in the radioresistant bacterium Deinococcus radiodurans. J Bacteriol 178: 4461-4471.
    Daly MJ, Ouyang L, Fuchs P & Minton KW (1994) In vivo damage and recA-dependent repair of plasmid and chromosomal DNA in the radiation-resistant bacterium Deinococcus radiodurans. J Bacteriol 176: 3508-3517.
    Daly MJ, Gaidamakova EK, Matrosova VY, et al. (2007) Protein oxidation implicated as the primary determinant of bacterial radioresistance. PLoS Biol 5: e92.
    Daly MJ, Gaidamakova EK, Matrosova VY, et al. (2004) Accumulation of Mn(11) in Deinococcus radiodurans facilitates gamma-radiation resistance. Science 306:1025-1028.
    Dennis RJ, Micossi E, McCarthy J, et al. (2006) Structure of the manganese superoxide dismutase from Deinococcus radiodurans in two crystal forms. Acta Crystallograph Sect F Struct Biol Cryst Commun 62:325-329.
    Diaz PI, Slakeski N, Reynolds EC, Morona R, Rogers AH & Kolenbrander PE (2006) Role of oxyR in the oral anaerobe Porphyromonas gingivalis. J Bacteriol 188:2454-2462.
    Domenech P, Honore N, Heym B & Cole ST (2001) Role of OxyS of Mycobacterium tuberculosis in oxidative stress:overexpression confers increased sensitivity to organic hydroperoxides. Microbes Infect 3:713-721.
    Earl AM, Mohundro MM, Mian IS & Battista JR (2002) The IrrE protein of Deinococcus radiodurans R1 is a novel regulator of recA expression. J Bacteriol 184:6216-6224.
    Elzbieta P & Janusz B (2003) Non-homologous DNA end joining. Acta Biochim Pol 50:891-908.
    Friedberg EC, Walker GC & Siebert W (1995) DNA repair and Muta-genesis. ASM Press, Washington, DC 14-31.
    Funayama T, Narumi I, Kikuchi M, Kitayama S, Watanabe H & Yamamoto K (1999) Identification and disruption analysis of the recN gene in the extremely radioresistant bacterium Deinococcus radiodurans. Mutat Res 435:151-161.
    Gao G, Lu H, Yin L & Hua Y (2007) Ring-like nucleoid does not play a key role in radioresistance of Deinococcus radiodurans. Sci China C Life Sci 50: 525-529.
    Ghosal D, Omelchenko MV, Gaidamakova EK, et al. (2005) How radiation kills cells:survival of Deinococcus radiodurans and Shewanella oneidensis under oxidative stress. FEMS Microbiol Rev 29:361-375.
    Gonzalez-Flecha B & Demple B (1999) Role for the oxyS gene in regulation of intracellular hydrogen peroxide in Escherichia coli. J Bacteriol 181:3833-3836. Goodhead DT (1994) Initial events in the cellular effects of ionizing radiation: clustered damage in DNA. Int J Radiat Biol 65:7-17.
    Grove A & Wilkinson SP (2005) Differential DNA binding and protection by dimeric and dodecameric forms of the ferritin homolog Dps from Deinococcus radiodurans. J Mol Biol 347:495-508.
    Gutman PD, Fuchs P, Ouyang L & Minton KW (1993) Identification, sequencing, and targeted mutagenesis of a DNA polymerase gene required for the extreme radioresistance of Deinococcus radiodurans. J Bacteriol 175: 3581-3590.
    Halliwell B (1994) Free radicala and antioxidants:a personal view. Nutr Rev 52: 253-265.
    Harrison A, Ray WC, Baker BD, Armbruster DW, Bakaletz LO & Munson RS, Jr. (2007) The OxyR regulon in nontypeable Haemophilus influenzae. J Bacteriol 189:1004-1012.
    Harsojo KS & Matsuyama A (1981) Genome multiplicity and radiation resistance in Micrococcus radiodurans. J Biochem (Tokyo) 90:877-880.
    Hattman S & Sun W (1997) Escherichia coli OxyR modulation of bacteriophage Mu mom expression in dam+cells can be attributed to its ability to bind hemimethylated Pmom promoter DNA. Nucleic Acids Res 25: 4385-4388.
    Hefferin ML & Tomkinson AE (2005) Mechanism of DNA double strand break repair by non-homologous end joining. DNA Repair (Amst) 4:639-648.
    Henderson IR & Owen P (1999) The major phase-variable outer membrane protein of Escherichia coli structurally resembles the immunoglobulin A1 protease class of exported protein and is regulated by a novel mechanism involving Dam and oxyR. J Bacteriol 181:2132-2141.
    Hirsch P, Gallikowski CA, Siebert J, et al. (2004) Deinococcus frigens sp. nov., Deinococcus saxicola sp. nov., and Deinococcus marmoris sp. nov., low temperature and draught-tolerating, UV-resistant bacteria from continental Antarctica. Syst Appl Microbiol 27:636-645.
    Hu Y, Tian B, Xu G, Yin L, Hua X, Lin J & Hua Y (2009) Characteristics of nuclease activity of the SbcCD complex from Deinococcus radiodurans. J Biochem 147:307-315.
    Hua Y & Gao G (2003) Comparative genomics of genes contributed to DNA repair in the radiation-resistant Deinococcus radiodurans. Wei Sheng Wu Xue Bao 43:120-126.
    Hua Y, Narumi I, Gao G, Tian B, Satoh K, Kitayama S & Shen B (2003) Pprl:a general switch responsible for extreme radioresistance of Deinococcus radiodurans. Biochem Biophys Res Commun 306:354-360.
    Huang L, Hua X, Lu H, Gao G, Tian B, Shen B & Hua Y (2007) Three tandem HRDC domains have synergistic effect on the RecQ functions in Deinococcus radiodurans. DNA Repair (Amst) 6:167-176.
    Huang LF, Zhang SW, Hua XT, Gao GJ & Hua YJ (2006a) Construction of the recQ double mutants and analysis of adversity in Deinococcus radiodurans. Wei Sheng Wu Xue Bao 46:205-209.
    Huang LF, Hua XT, Lu HM, Gao GJ, Tian B, Shen BH & Hua YJ (2006b) Functional analysis of helicase and three tandem HRDC domains of RecQ in Deinococcus radiodurans. J Zhejiang Univ Sci B 7:373-376.
    Iliakis G (1991) The role of DNA double strand breaks in ionizing radiation induced killing of eukaryotic cells. Bioessays 13:641-648.
    Imlay JA (2003) Pathways of oxidative damage. Annu Rev Microbiol 57: 395-418.
    Kamble VA & Misra HS (2010) The SbcCD complex of Deinococcus radiodurans contributes to radioresistance and DNA strand break repair in vivo and exhibits Mre 11-Rad50 type activity in vitro. DNA Repair (Amst).
    Khaimar NP, Misra HS & Apte SK (2003) Pyrroloquinoline-quinone synthesized in Escherichia coli by pyrroloquinoline-quinone synthase of Deinococcus radiodurans plays a role beyond mineral phosphate solubilization. Biochem Biophys Res Commun 312:303-308.
    Kim JA & Mayfield J (2000) Identification of Brucella abortus OxyR and its role in control of catalase expression. J Bacteriol 182:5631-5633.
    Kim SG, Bhattacharyya G, Grove A & Lee YH (2006) Crystal structure of Dps-1, a functionally distinct Dps protein from Deinococcus radiodurans. J Mol Biol 361:105-114.
    Kim SO, Merchant K, Nudelman R, et al. (2002) OxyR:a molecular code for redox-related signaling. Cell 109:383-396.
    Kitayama S, Narumi I, Kikuchi M & Watanabe H (2000) Mutation in recR gene of Deinococcus radiodurans and possible involvement of its product in the repair of DNA interstrand cross-links. Mutat Res 461:179-187.
    Kobayashi I, Tamura T, Sghaier H, Narumi I, Yamaguchi S, Umeda K & Inagaki K (2006) Characterization of monofunctional catalase KatA from radioresistant bacterium Deinococcus radiodurans. J Biosci Bioeng 101:315-321.
    Kullik I, Stevens J, Toledano MB & Storz G (1995) Mutational analysis of the redox-sensitive transcriptional regulator OxyR:regions important for DNA binding and multimerization. J Bacteriol 177:1285-1291.
    Lange CC, Wackett LP, Minton KW & Daly MJ (1998) Engineering a recombinant Deinococcus radiodurans for organopollutant degradation in radioactive mixed waste environments. Nat Biotechnol 16:929-933.
    Lau GW, Britigan BE & Hassett DJ (2005) Pseudomonas aeruginosa OxyR is required for full virulence in rodent and insect models of infection and for resistance to human neutrophils. Infect Immun 73:2550-2553.
    Le D, Hua X, Huang L, et al. (2008) Biochemical characterization of two DNA ligases from Deinococcus radiodurans. Protein Pept Lett 15:600-605.
    Lecointe F, Coste G, Sommer S & Bailone A (2004a) Vectors for regulated gene expression in the radioresistant bacterium Deinococcus radiodurans. Gene 336:25-35.
    .Lecointe F, Shevelev IV, Bailone A, Sommer S & Hubscher U (2004b) Involvement of an X family DNA polymerase in double-stranded break repair in the radioresistant organism Deinococcus radiodurans. Mol Microbiol 53: 1721-1730.
    Levin-Zaidman S, Englander J, Shimoni E, Sharma AK, Minton KW & Minsky A (2003) Ringlike structure of the Deinococcus radiodurans genome:a key to radioresistance? Science 299:254-256.
    Loprasert S, Sallabhan R, Whangsuk W & Mongkolsuk S (2002) The Burkholderia pseudomallei oxyR gene:expression analysis and mutant characterization. Gene 296:161-169.
    Maciver I & Hansen EJ (1996) Lack of expression of the global regulator OxyR in Haemophilus influenzae has a profound effect on growth phenotype. Infect Immun 64:4618-4629.
    Makarova KS, Aravind L, Wolf YI, Tatusov RL, Minton KW, Koonin EV & Daly MJ (2001) Genome of the extremely radiation-resistant bacterium Deinococcus radiodurans viewed from the perspective of comparative genomics. Microbiol Mol Biol Rev 65:44-79.
    Markillie LM, Varnum SM, Hradecky P & Wong KK (1999) Targeted mutagenesis by duplication insertion in the radioresistant bacterium Deinococcus radiodurans:radiation sensitivities of catalase (katA) and superoxide dismutase (sodA) mutants. J Bacteriol 181:666-669.
    Mattimore V & Battista JR (1996) Radioresistance of Deinococcus radiodurans: functions necessary to survive ionizing radiation are also necessary to survive prolonged desiccation. J Bacteriol 178:633-637.
    Meima R & Lidstrom ME (2000) Characterization of the minimal replicon of a cryptic Deinococcus radiodurans SARK plasmid and development of versatile Escherichia coli-D. radiodurans shuttle vectors. Appl Environ Microbiol 66: 3856-3867.
    Melstrom KA Jr, Kozlowski R, Hassett DJ, et al. (2007) Cytotoxicity of Pseudomonas secreted exotoxins requires OxyR expression. J Surg Res 143: 50-57.
    Minton KW (1994) DNA repair in the extremely radioresistant bacterium Deinococcus radiodurans. Mol Microbiol 13:9-15.
    Minton KW (1996) Repair of ionizing-radiation damage in the radiation resistant bacterium Deinococcus radiodurans. Mutat Res 363:1-7.
    Misra HS, Khairnar NP, Barik A, Indira Priyadarsini K, Mohan H & Apte SK (2004) Pyrroloquinoline-quinone:a reactive oxygen species scavenger in bacteria. FEBS Lett 578:26-30.
    Mongkolsuk S, Sukchawalit R, Loprasert S, Praituan W & Upaichit A (1998) Construction and physiological analysis of a Xanthomonas mutant to examine the role of the oxyR gene in oxidant-induced protection against peroxide killing. J Bacteriol 180:3988-3991.
    Mortimer RK (1958) Radiobiological and genetic studies on a polyploid series (haploid to hexaploid) of Saccharomyces cerevisiae. Radiat Res 66:158-169.
    Moseley BE & Evans DM (1983) Isolation and properties of strains of Micrococcus (Deinococcus) radiodurans unable to excise ultraviolet light-induced pyrimidine dimers from DNA:evidence for two excision pathways. J Gen Microbiol 129:2437-2445.
    Mukhopadhyay S & Schellhorn HE (1997) Identification and characterization of hydrogen peroxide-sensitive mutants of Escherichia coli:genes that require OxyR for expression. J Bacteriol 179:330-338.
    Murakami M, Narumi I, Satoh K, Furukawa A & Hayata I (2006) Analysis of interaction between DNA and Deinococcus radiodurans PprA protein by atomic force microscopy. Biochim Biophys Acta 1764:20-23.
    Nakjarung K, Mongkolsuk S & Vattanaviboon P (2003) The oxyR from Agrobacterium tumefaciens:evaluation of its role in the regulation of catalase and peroxide responses. Biochem Biophys Res Commun 304:41-47.
    Narumi I, Satoh K, Cui S, Funayama T, Kitayama S & Watanabe H (2004) PprA:a novel protein from Deinococcus radiodurans that stimulates DNA ligation. Mol Microbiol 54:278-285.
    Ochsner UA, Vasil ML, Alsabbagh E, Parvatiyar K & Hassett DJ (2000) Role of the Pseudomonas aeruginosa oxyR-recG operon in oxidative stress defense and DNA repair:OxyR-dependent regulation of katB-ankB, ahpB, and ahpC-ahpF. J Bacteriol 182:4533-4544.
    Omelchenko MV, Wolf YI, Gaidamakova EK, et al. (2005) Comparative genomics of Thermus thermophilus and Deinococcus radiodurans:divergent routes of adaptation to thermophily and radiation resistance. BMC Evol Biol 5: 57.
    Pask-Hughes RA & Shaw N (1982) Glycolipids from some extreme thermophilic bacteria to the genus Thermus. J Bacteriol 149:54-58.
    Pitcher RS, Wilson TE & Doherty AJ (2005) New insights into NHEJ repair processes in prokaryotes. Cell Cycle 4:675-678
    Pomposiello PJ & Demple B (2001) Red ox-operated genetic switches:the SoxR and OxyR transcription factors. Trends Biotechnol 19:109-114.
    Quintela JC, Garcia-del Portillo F, Pittenauer E, Allmaier G & de Pedro MA (1999) Peptidoglycan fine structure of the radiotolerant bacterium Deinococcus radiodurans Sark. J Bacteriol 181:334-337.
    Rainey FA, Nobre MF, Schumann P, Stackebrandt E & da Costa MS (1997) Phylogenetic diversity of the deinococci as determined by 16S ribosomal DNA sequence comparison. Int J Syst Bacteriol 47:510-514.
    Rainey FA, Ferreira M, Nobre MF, et al. (2007) Deinococcus peraridilitoris sp. nov., isolated from a coastal desert. Int J Syst Evol Microbiol 57:1408-1412.
    Rainey FA, Ray K, Ferreira M, et al. (2005) Extensive diversity of ionizing-radiation-resistant bacteria recovered from Sonoran Desert soil and description of nine new species of the genus Deinococcus obtained from a single soil sample. Appl Environ Microbiol 71:5225-5235.
    Riley PA (1994) Free radicals in biology:oxidative stress and the effects of ionizing radiation. Int J Radiat Biol 65:27-33.
    Seib KL, Wu HJ, Srikhanta YN, et al. (2007) Characterization of the OxyR regulon of Neisseria gonorrhoeae. Mol Microbiol 63:54-68.
    Servinsky MD & Julin DA (2007) Effect of a recD mutation on DNA damage resistance and transformation in Deinococcus radiodurans. J Bacteriol 189: 5101-5107.
    Storz G & Imlay JA (1999) Oxidative stress. Curr Opin Microbiol 2:188-194.
    Sun W & Hattman S (1996) Escherichia coli OxyR protein represses the unmethylated bacteriophage Mu mom operon without blocking binding of the transcriptional activator C. Nucleic Acids Res 24:4042-4049.
    Sun Z, Shen S, Tian B, Wang H, Xu Z, Wang L & Hua Y (2009a) Functional analysis of gamma-carotene ketolase involved in the carotenoid biosynthesis of Deinococcus radiodurans. FEMS Microbiol Lett 301:21-27.
    Sun Z, Shen S, Wang C, et al. (2009b) A novel carotenoid 1,2-hydratase (CruF) from two species of the non-photosynthetic bacterium Deinococcus. Microbiology 155:2775-2783.
    Thompson BG, Anderson R & Murray R (1980) Unusual polar lipids of Micrococcus radiodurans strain SARK. Can J Microbiol 26:1408-1411.
    Thornley MJ (1963) Radiation resistance among bacteria. J Appl Bacteriol 26: 539-547.
    Tian B, Xu Z, Sun Z, Lin J & Hua Y (2007) Evaluation of the antioxidant effects of carotenoids from Deinococcus radiodurans through targeted mutagenesis, chemiluminescence, and DNA damage analyses. Biochim Biophys Acta 1770: 902-911.
    Tian B, Wu Y, Sheng D, Zheng Z, Gao G & Hua Y (2004) Chemiluminescence assay for reactive oxygen species scavenging activities and inhibition on oxidative damage of DNA in Deinococcus radiodurans. Luminescence 19: 78-84.
    Tian B, Sun Z, Xu Z, Shen S, Wang H & Hua Y (2008) Carotenoid 3',4'-desaturase is involved in carotenoid biosynthesis in the radioresistant bacterium Deinococcus radiodurans. Microbiology 154:3697-3706.
    Tian B, Sun Z, Shen S, et al. (2009) Effects of carotenoids from Deinococcus radiodurans on protein oxidation. Lett Appl Microbiol 49:689-694.
    Tseng.HJ, McEwan AG, Apicella MA & Jennings MP (2003) OxyR acts as a repressor of catalase expression in Neisseria gonorrhoeae. Infect Immun 71: 550-556.
    Venkateswaran A, McFarlan SC, Ghosal D, et al. (2000) Physiologic determinants of radiation resistance in Deinococcus radiodurans. Appl Environ Microbiol 66:2620-2626.
    Wallecha A, Correnti J, Munster V & van der Woude M (2003) Phase variation of Ag43 is independent of the oxidation state of OxyR. J Bacteriol 185: 2203-2209.
    Wang P & Schellhorn HE (1995) Induction of resistance to hydrogen peroxide and radiation in Deinococcus radiodurans. Can J Microbiol 41:170-176.
    Wang X, Mukhopadhyay P, Wood MJ, Outten FW, Opdyke JA & Storz G (2006) Mutational analysis to define an activating region on the redox-sensitive transcriptional regulator OxyR. J Bacteriol 188:8335-8342.
    Webe KJ & Flentjie M (1993) Lethality of heavy ion-induced DNA double-strand breaks in mammalian cells. Int J Radiat Biol 64:169-178.
    Weller GR, Kysela B, Roy R, et al. (2002) Identification of a DNA nonhomologous end-joining complex in bacteria. Science 297:1686-1689.
    White O, Eisen JA, Heidelberg JF, et al. (1999) Genome sequence of the radioresistant bacterium Deinococcus radiodurans R1. Science 286: 1571-1577.
    Wu J, Lin X & Xie H (2008) OxyR is involved in coordinate regulation of expression of fimA and sod genes in Porphyromonas gingivalis. FEMS Microbiol Lett 282:188-195.
    Xu G, Wang L, Chen H, Lu H, Ying N, Tian B & Hua Y (2008) RecO is essential for DNA damage repair in Deinococcus radiodurans. J Bacteriol 190: 2624-2628.
    Xu Z, Tian B, Sun Z, Lin J & Hua Y (2007) Identification and functional analysis of a phytoene desaturase gene from the extremely radioresistant bacterium Deinococcus radiodurans. Microbiology 153:1642-1652.
    Yan ZY, Xu ZJ, Xu GZ, Tian B & Hua YJ (2007) Construction of a dps mutant and its functional analysis in Deinococcus radiodurans. Wei Sheng Wu Xue Bao 47:610-615.
    Yang Y, Itoh T, Yokobori S, et al. (2009) Deinococcus aerius sp. nov., isolated from the high atmosphere. Int J Syst Evol Microbiol 59:1862-1866.
    Yang Y, Itoh T, Yokobori S, et al. (2010) Deinococcus aetherius sp. nov., isolated from the stratosphere. Int J Syst Evol Microbiol 60:776-779.
    Yuan M, Zhang W, Dai S, et al. (2009) Deinococcus gobiensis sp. nov., an extremely radiation-resistant bacterium. Int J Syst Evol Microbiol 59: 1513-1517.
    Yun EJ & Lee YN (2000) Production of two different catalase-peroxidases by Deinococcus radiophilus. FEMS Microbiol Lett 184:155-159.
    Zahradka K, Slade D, Bailone A, et al. (2006) Reassembly of shattered chromosomes in Deinococcus radiodurans. Nature 443:569-573.
    Zhang A, Altuvia S, Tiwari A, Argaman L, Hengge-Aronis R & Storz G (1998) The OxyS regulatory RNA represses rpoS translation and binds the Hfq (HF-I) protein. Embo J 17:6061-6068.
    Zhang SL, Shen JG, Xu PH, et al. (2007) A novel genotypic test for rapid detection of multidrug-resistant Mycobacterium tuberculosis isolates by a multiplex probe array. J Appl Microbiol 103:1262-1271.
    Zheng M & Storz G (2000) Redox sensing by prokaryotic transcription factors. Biochem Pharmacol 59:1-6.
    Zheng M, Aslund F & Storz G (1998) Activation of the OxyR transcription factor by reversible disulfide bond formation. Science 279:1718-1721.
    Zheng M, Wang X, Templeton LJ, Smulski DR, LaRossa RA & Storz G (2001a) DNA microarray-mediated transcriptional profiling of the Escherichia coli
    response to hydrogen peroxide. J Bacteriol 183:4562-4570. Zheng M, Wang X, Doan B, Lewis KA, Schneider TD & Storz G (2001b) Computation-directed identification of OxyR DNA binding sites in Escherichia coli. J Bacteriol 183:4571-4579.
    Zimmerman JM & Battista JR (2005) A ring-like nucleoid is not necessary for radioresistance in the Deinococcaceae. BMC Microbiol 5:17.
    Battista JR, Earl AM & Park MJ (1999) Why is Deinococcus radiodurans so resistant to ionizing radiation? Trends Microbiol7:362-365.
    Blasius M, Sommer S & Hubscher U (2008) Deinococcus radiodurans:what belongs to the survival kit? Crit Rev Biochem Mol Biol 43:221-238.
    Chen H, Xu G, Zhao Y, et al. (2008) A novel OxyR sensor and regulator of hydrogen peroxide stress with one cysteine residue in Deinococcus radiodurans. PLoS ONE 3:e1602.
    Choi H, Kim S, Mukhopadhyay P, Cho S, Woo J, Storz G & Ryu S (2001) Structural basis of the redox switch in the OxyR transcription factor. Cell 105: 103-113.
    Cox MM & Battista JR (2005) Deinococcus radiodurans-the consummate survivor. Nat Rev Microbiol 3:882-892.
    Fuangthong M & Helmann JD (2002) The OhrR repressor senses organic hydroperoxides by reversible formation of a cysteine-sulfenic acid derivative. Proc Natl Acad Sci U S A 99:6690-6695.
    Funayama T, Narumi I, Kikuchi M, Kitayama S, Watanabe H & Yamamoto K (1999) Identification and disruption analysis of the recN gene in the extremely radioresistant bacterium Deinococcus radiodurans. Mutat Res 435:151-161.
    Gao G, Lu H, Huang L & Hua Y (2005) Construction of DNA damage response gene pprl function-deficient and function-complementary mutants in Deinococcus radiodurans. Chinese Sci Bull 50:311-316.
    Ghosal D, Omelchenko MV, Gaidamakova EK, et al. (2005) How radiation kills cells:survival of Deinococcus radiodurans and Shewanella oneidensis under oxidative stress. FEMS Microbiol Rev 29:361-375.
    Hua Y, Narumi I, Gao G, Tian B, Satoh K, Kitayama S & Shen B (2003) Pprl:a general switch responsible for extreme radioresistance of Deinococcus radiodurans. Biochem Biophys Res Commun 306:354-360.
    Imlay JA (2003) Pathways of oxidative damage. Annu Rev Microbiol 57: 395-418.
    Kullik I, Stevens J, Toledano MB & Storz G (1995) Mutational analysis of the redox-sensitive transcriptional regulator OxyR:regions important for DNA binding and multimerization. J Bacteriol 177:1285-1291.
    Lange CC, Wackett LP, Minton KW & Daly MJ (1998) Engineering a recombinant Deinococcus radiodurans for organopollutant degradation in radioactive mixed waste environments. Nat Biotechnol 16:929-933.
    Minton KW (1994) DNA repair in the extremely radioresistant bacterium Deinococcus radiodurans. Mol Microbiol 13:9-15.
    Mongkolsuk S & Helmann JD (2002) Regulation of inducible peroxide stress responses. Mol Microbiol 45:9-15.
    Moseley BE & Evans DM (1983) Isolation and properties of strains of Micrococcus (Deinococcus) radiodurans unable to excise ultraviolet light-induced pyrimidine dimers from DNA:evidence for two excision pathways. J Gen Microbiol 129:2437-2445.
    Pomposiello PJ & Demple B (2001) Redox-operated genetic switches:the SoxR and OxyR transcription factors. Trends Biotechnol 19:109-114.
    Sambrook J, Fritsch EF & Maniatis T (1989) Molecular Cloning. A Laboratory Manual. Cold Spring Harbor Laboratory, Cold Spring Harbor.
    Storz G & Imlay JA (1999) Oxidative stress. Curr Opin Microbiol 2:188-194.
    Tanaka M, Earl AM, Howell HA, Park MJ, Eisen JA, Peterson SN & Battista JR (2004) Analysis of Deinococcus radiodurans's transcriptional response to ionizing radiation and desiccation reveals novel proteins that contribute to extreme radioresistanc. Genetics 168:21-33.
    Tanaka M, Narumi I, Funayama T, et al. (2005) Characterization of pathways dependent on the uvsE, uvrA1, or uvrA2 gene product for UV resistance in Deinococcus radiodurans. J Bacteriol 187:3693-3697.
    Wang X, Mukhopadhyay P, Wood MJ, Outten FW, Opdyke JA & Storz G (2006) Mutational analysis to define an activating region on the redox-sensitive transcriptional regulator OxyR. J Bacteriol 188:8335-8342.
    White O, Eisen JA, Heidelberg JF, et al. (1999) Genome sequence of the radioresistant bacterium Deinococcus radiodurans R1. Science 286: 1571-1577.
    Zheng M & Storz G (2000) Redox sensing by prokaryotic transcription factors. Biochem Pharmacol 59:1-6.
    Zheng M, Aslund F & Storz G (1998) Activation of the OxyR transcription factor by reversible disulfide bond formation. Science 279:1718-1721.
    Carbonneau MA, Melin AM, Perromat A & Clerc M (1989) The action of free radicals on Deinococcus radiodurans carotenoids. Arch Biochem Biophys 275: 244-251.
    Chen H, Xu G, Zhao Y, et al. (2008) A novel OxyR sensor and regulator of hydrogen peroxide stress with one cysteine residue in Deinococcus radiodurans. PLoS ONE 3:e1602.
    Gao G, Lu H, Huang L & Hua Y (2005) Construction of DNA damage response gene pprl function-deficient and function-complementary mutants in Deinococcus radiodurans. Chinese Sci Bull 50:311-316.
    Hahn JS, Oh SY & Roe JH (2002) Role of OxyR as a peroxide-sensing positive regulator in Streptomyces coelicolor A3(2). J Bacteriol 184: 5214-5222.
    Hua Y, Narumi I, Gao G, Tian B, Satoh K, Kitayama S & Shen B (2003) Pprl:a general switch responsible for extreme radioresistance of Deinococcus radiodurans. Biochem Biophys Res Commun 306:354-360.
    Kota S & Misra HS (2006) PprA:A protein implicated in radioresistance of Deinococcus radiodurans stimulates catalase activity in Escherichia coli. Appl Microbiol Biotechnol 72:790-796.
    Lin J, Qi R, Aston C, et al. (1999) Whole-genome shotgun optical mapping of Deinococcus radiodurans. Science 285:1558-1562.
    Loprasert S, Sallabhan R, Whangsuk W & Mongkolsuk S (2002) The Burkholderia pseudomallei oxyR gene:expression analysis and mutant characterization. Gene 296:161-169.
    Michael F. Christman, Robin W. Morgan, Fredric S. Jacobson & Ames BN (1985) Positive control of a regulon for defenses against oxidative stress and some heat-shock proteins in Salmonella typhimurium. Cell 41:753-762.
    Mongkolsuk S & Helmann JD (2002) Regulation of inducible peroxide stress responses. Mol Microbiol 45:9-15.
    Mongkolsuk S, Sukchawalit R, Loprasert S, Praituan W & Upaichit A (1998) Construction and physiological analysis of a Xanthomonas mutant to examine the role of the oxyR gene in oxidant-induced protection against peroxide killing. J Bacteriol 180:3988-3991.
    Nishimura A, Morita M, Nishimura Y & Sugino Y (1990) A rapid and highly efficient method for preparation of competent Escherichia coli cells. Nucleic Acids Res 18:6169.
    Sheng D, Gao G, Tian B, Xu Z, Zheng Z & Hua Y (2005) RecX is involved in antioxidant mechanisms of the radioresistant bacterium Deinococcus radiodurans. FEMS Microbiol Lett 244:251-257.
    Storz G & Tartaglia LA (1992) OxyR:a regulator of antioxidant genes. J Nutr 122:627-630.
    Tian B, Xu Z, Sun Z, Lin J & Hua Y (2007) Evaluation of the antioxidant effects of carotenoids from Deinococcus radiodurans through targeted mutagenesis, chemiluminescence, and DNA damage analyses. Biochim Biophys Acta 1770: 902-911.
    Wang L, Xu G, Chen H, Zhao Y, Xu N, Tian B & Hua Y (2008) DrRRA:a novel response regulator essential for the extreme radioresistance of Deinococcus radiodurans. Mol Microbiol 67:1211-1222.
    Zheng M, Aslund F & Storz G (1998) Activation of the OxyR transcription factor by reversible disulfide bond formation. Science 279:1718-1721.
    Andrews SC, Robinson AK & Rodriguez-Quinones F (2003) Bacterial iron homeostasis. FEMS Microbiol Rev 27:215-237.
    Chen H, Xu Z, Tian B, Chen W, Hu S & Hua Y (2007) Transcriptional profile in response to ionizing radiation at low dose in Deinococcus radiodurans. Prog nat sci 17:529-536.
    Chen H, Huang L, Hua X, et al. (2009) Pleiotropic effects of RecQ in Deinococcus radiodurans. Genomics 94:333-340.
    Ghosh S & Grove A (2006) The Deinococcus radiodurans-encoded HU protein has two DNA-binding domains. Biochemistry 45:1723-1733.
    Hua Y, Narumi I, Gao G, Tian B, Satoh K, Kitayama S & Shen B (2003) Pprl:a general switch responsible for extreme radioresistance of Deinococcus radiodurans. Biochem Biophys Res Commun 306:354-360.
    Kota S & Misra HS (2006) PprA:A protein implicated in radioresistance of Deinococcus radiodurans stimulates catalase activity in Escherichia coli. Appl Microbiol Biotechnol 72:790-796.
    Lander HM (1997) An essential role for free radical and derived species in signal transduction. Faseb J 11:118-124.
    Livak KJ & Schmittgen TD (2001) Analysis of Relative Gene Expression Data Using Real-Time Quantitative PCR and the 2-ΔΔCT Method. Methods 25: 402-408.
    Mongkolsuk S & Helmann JD (2002) Regulation of inducible peroxide stress responses. Mol Microbiol 45:9-15.
    Pomposiello PJ & Demple B (2001) Redox-operated genetic switches:the SoxR and OxyR transcription factors. Trends Biotechnol 19:109-114.
    Seaver LC & Imlay JA (2004) Are respiratory enzymes the primary sources of intracellular hydrogen peroxide? J Biol Chem 279:48742-48750.
    Sheng D, Gao G, Tian B, Xu Z, Zheng Z & Hua Y (2005) RecX is involved in antioxidant mechanisms of the radioresistant bacterium Deinococcus radiodurans. FEMS Microbiol Lett 244:251-257.
    Storz G & Imlay JA (1999) Oxidative stress. Curr Opin Microbiol 2:188-194.
    Tanaka M, Earl AM, Howell HA, Park MJ, Eisen JA, Peterson SN & Battista JR (2004) Analysis of Deinococcus radiodurans's transcriptional response to ionizing radiation and desiccation reveals novel proteins that contribute to extreme radioresistance. Genetics 168:21-33.
    Wang L, Xu G, Chen H, Zhao Y, Xu N, Tian B & Hua Y (2008) DrRRA:a novel response regulator essential for the extreme radioresistance of Deinococcus radiodurans. Mol Microbiol 67:1211-1222.
    Wettenhall JM & Smyth GK (2004) limmaGUI:a graphical user interface for linear modeling of microarray data. Bioinformatics 20:3705-3706.
    White O, Eisen JA, Heidelberg JF, et al. (1999) Genome sequence of the radioresistant bacterium Deinococcus radiodurans R1. Science 286: 1571-1577.
    Xiang Z, Yang Y, Ma X & Ding W (2003) Microarray expression profiling: analysis and applications. Curr Opin Drug Discov Devel 6:384-395.
    Yang YH, Dudoit S, Luu P, Lin DM, Peng V, Ngai J & Speed TP (2002) Normalization for cDNA microarray data:a robust composite method addressing single and multiple slide systematic variation. Nucleic Acids Res 30: e15.
    Zhou Q, Zhang X, Xu H, Xu B & Hua Y (2007) A new role of Deinococcus radiodurans RecD in antioxidant pathway. FEMS Microbiol Lett 271:118-125.
    Battista JR (1997) Against all odds:the survival strategies of Deinococcus radiodurans. Annu Rev Microbiol 51:203-224.
    Bauermeister A, Bentchikou E, Moeller R & Rettberg P (2009) Roles of PprA, IrrE, and RecA in the resistance of Deinococcus radiodurans to germicidal and environmentally relevant UV radiation. Arch Microbiol.
    Blasius M, Sommer S & Hubscher U (2008) Deinococcus radiodurans:what belongs to the survival kit? Crit Rev Biochem Mol Biol 43:221-238.
    Chang X, Yang L, Zhao Q, et al. (2010) Involvement of recF in 254 nm Ultraviolet Radiation Resistance in Deinococcus radiodurans and Escherichia coli. Curr Microbiol Epub ahead of print
    Courcelle J, Khodursky A, Peter B, Brown PO & Hanawalt PC (2001) Comparative gene expression profiles following UV exposure in wild-type and SOS-deficient Escherichia coli. Genetics 158:41-64.
    Earl AM, Mohundro MM, Mian IS & Battista JR (2002) The IrrE protein of Deinococcus radiodurans R1 is a novel regulator of recA expression. J Bacteriol 184:6216-6224.
    Gascon J, Oubina A, Perez-Lezaun A & Urmeneta J (1995) Sensitivity of selected bacterial species to UV radiation. Curr Microbiol 30:177-182.
    Gotz D, Paytubi S, Munro S, Lundgren M, Bernander R & White MF (2007) Responses of hyperthermophilic crenarchaea to UV irradiation. Genome Biol 8: R220.
    Grove A & Wilkinson SP (2005) Differential DNA binding and protection by dimeric and dodecameric forms of the ferritin homolog Dps from Deinococcus radiodurans. J Mol Biol 347:495-508.
    Hua Y, Narumi I, Gao G, Tian B, Satoh K, Kitayama S & Shen B (2003) Pprl:a general switch responsible for extreme radioresistance of Deinococcus radiodurans. Biochem Biophys Res Commun 306:354-360.
    Kim SG, Bhattacharyya G, Grove A & Lee YH (2006) Crystal structure of Dps-1, a functionally distinct Dps protein from Deinococcus radiodurans. J Mol Biol 361:105-114.
    Kota S & Misra HS (2006) PprA:A protein implicated in radioresistance of Deinococcus radiodurans stimulates catalase activity in Escherichia coli. Appl Microbiol Biotechnol 72:790-796.
    Makarova KS, Aravind L, Wolf YI, Tatusov RL, Minton KW, Koonin EV & Daly MJ (2001) Genome of the extremely radiation-resistant bacterium Deinococcus radiodurans viewed from the perspective of comparative genomics. Microbiol Mol Biol Rev 65:44-79.
    Moseley BE & Evans DM (1983) Isolation and properties of strains of Micrococcus (Deinococcus) radiodurans unable to excise ultraviolet light-induced pyrimidine dimers from DNA:evidence for two excision pathways. J Gen Microbiol 129:2437-2445.
    Narumi I, Satoh K, Cui S, Funayama T, Kitayama S & Watanabe H (2004) PprA:a novel protein from Deinococcus radiodurans that stimulates DNA ligation. Mol Microbiol 54:278-285.
    Narumi I, Satoh K, Kikuchi M, et al. (2001) The LexA protein from Deinococcus radiodurans is not involved in RecA induction following gamma irradiation. J Bacteriol 183:6951-6956.
    Patel BA, Moreau M, Widom J, Chen H, Yin L, Hua Y & Crane BR (2009) Endogenous nitric oxide regulates the recovery of the radiation-resistant bacterium Deinococcus radiodurans from exposure to UV light. Proc Natl Acad SciUSA106:18183-18188.
    Quillardet P, Rouffaud MA & Bouige P (2003) DNA array analysis of gene expression in response to UV irradiation in Escherichia coli. Res Microbiol 154: 559-572.
    Sheng D, Zheng Z, Tian B, Shen B & Hua Y (2004) LexA analog (dra0074) is a regulatory protein that is irrelevant to recA induction. J Biochem (Tokyo) 136: 787-793.
    Shinagawa H (1996) SOS response as an adaptive response to DNA damage in prokaryotes. Exs 77:221-235.
    Sukhi SS, Shashidhar R, Kumar SA & Bandekar JR (2009) Radiation resistance of Deinococcus radiodurans R1 with respect to growth phase. FEMS Microbiol Lett 297:49-53.
    Tanaka M, Narumi I, Funayama T, et al. (2005) Characterization of pathways dependent on the uvsE, uvrA1, or uvrA2 gene product for UV resistance in Deinococcus radiodurans. J Bacteriol 187:3693-3697.
    Waldron DE, Owen P & Dorman CJ (2002) Competitive interaction of the OxyR DNA-binding protein and the Dam methylase at the antigen 43 gene regulatory region in Escherichia coli. Mol Microbiol 44:509-520.
    White O, Eisen JA, Heidelberg JF, et al. (1999) Genome sequence of the radioresistant bacterium Deinococcus radiodurans R1. Science 286: 1571-1577.

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