Raymond Devoret (à droite) avec ses collaboratrices Adriana Bailone (à gauche) et Suzanne Sommer (au milieu) en 1990
© Collection personnelle d’Adriana Bailone
1- Devoret R, Levy C. Aspects biologiques et médicaux de la radioprotection, dans Radiobiologie Appliquée, Gauthier Villars Ed. Paris (1965) chapitre 18, p. 775-804.
2- Markovich H, Devoret R. The effect of small doses of ionizing radiations on Escherichia coli. Internat. J. of Rad. Biol. (1959) p. 293-303.
3- Lwoff A, Siminovitch L, Kjeldgaard N. Induction de la production de bactériophages chez une bactérie lysogène. Ann. Inst. Pasteur 79 (1950), p. 815-859.
4- Latarjet R. Induction par rayons X de la production de bactériophages chez B. megatherium lysogénique. Ann. Inst. Pasteur 81 (1951), p. 389-393.
5- Markovich H, Latarjet R. Radiobiological aspects of the induction of lysogenic bacteria to produce phage with x-ray, gamma ray and ultraviolet radiations. Adv. Biol. Med. Phys. 6 (1958), p. 75-94.
6- Borek E, Ryan A The transfer of irradiation-elicited induction in a lysogenic organism, Proc. Nat. Acad. Sci. USA 44 (1958), p. 374-377.
7- Borek E, Ryan A. The transfer of a biologically active irradiation product from cell to cell, Biochim. Biophys. Acta 41 (1960), p. 67-73.
8- Devoret R, George J. Sur l’action inductrice du rayonnement ultraviolet après conjugaison chez Escherichia coli K12, C. R. Acad. Sc. Paris 258 (1964), p. 2227-2230.
9- Devoret R, George J. Sur un facteur extra-chromosomique responsable de l’induction ultraviolette par conjugaison chez Escherichia coli K12, C. R. Acad. Sc. Paris 258 (1964), p. 5287-5290.
10- Devoret R, George J. Induction indirecte du prophage λ par le rayonnement ultraviolet, Mutation Res. 4 (1967), p. 713-734.
11- George J, Devoret R. Conjugal transfer of UV-damaged F-prime sex factors and indirect induction of prophage λ, Molec. Gen. Genet 111 (1971), p. 103-119
12- Devoret R. Influence du génotype de la bactérie hôte sur la mutation du phage λ produite par le rayonnement ultraviolet, C. R. Acad. Sci. Paris 260 (1965), p. 1510-1513
13- Brooks, K., and A. J. Clark. Behaviour of a bacteriophage in a recombination-deficient strain of Escherichia coli. J. Virol. 1 (1967) p. 283-293.
14- Devoret R, Blanco M. Mutants of Escherichia coli K12 (λ)+ non-inducible by thymine deprivation. I Method of isolation and classes of mutants obtained, Molec. Gen. Genet. 107 (1970), p. 272-280.
15- Ames B, Durston WE, YamasakiE, Lee FD. Carcinogens are mutagens : a simple test system combining liver homogenates for activation and bacteria for detection. Proc. Nat. Acad. Sci. USA 70 (1973), p. 2281-2285.
16- Moreau PL, Bailone A, Devoret R. Prophage λ induction in Escherichia coli K12 envA uvrB : a highly sensitive test for potential carcinogens. Proc. Nat. Acad. Sci. (1976) 73, p. 3700-3704.
17- Radman M. in Molecular and environmental aspects of mutagenesis, Thomas C. Ed, Springfield, Illinois. (1974) p. 128.
18- Radman M. SOS repair hypothesis : Phenomenology of an inducible DNA repair which is accompanied by mutagenesis. In Molecular mechanisms for repair of DNA, Hanawalt P. and Setlow R.B. Eds, Plenum Press, New York (1975) p. 355-367.
19- Devoret R. The regulatory role of radiation of DNA, Pollard E.C. and Bockrath R.C. Eds, Gainsville. (1975).
20- Witkin EM. Ultraviolet mutagenesis and inducible DNA repair in Escherichia coli. Bact. Rev. 40 (1976), p. 869-907.
21- Bailone A, Blanco M, Devoret R. E.coli K12 inf : a mutant deficient in prophage λ induction and cell filamentation. Molec. Gen. Genet. 136 (1975), p. 291-307.
22- Bailone A, Levine A, Devoret R. Inactivation of prophage lambda repressor in vivo. J. Mol. Biol. 131 (1979), p. 553-572.
23- Dutreix M, Bailone A, Devoret R. Efficiency of induction of prophage lambda mutants as a function of recA alleles. J. Bacteriol. 161(3) (1985), p. 1080-1085.
24- Morand P, Blanco M, Devoret R. Characterization of lexB mutations in Escherichia coli K-12. J. Bacteriol. 131(2) (1977), p. 572-582.
25- Roberts JW, Roberts CW. Proteolytic cleavage of bacteriophage λ repressor in induction. Proc. Nat. Acad. Sci. USA. 72(1) (1975), p. 147-151.
26- Roberts JW, Roberts CW, Craig NL. Escherichia coli recA gene product inactivates phage λ repressor. Proc. Natl. Acad. Sci. USA 75(10) (1978), p. 4714-4718.
27- Craig NL, Roberts JW. Function of nucleoside triphosphate and polynucleotide in Escherichia coli RecA protein-directed cleavage of phage λ repressor. J. Biol. Chem. 256(15) (1981), p. 8039-8044.
28- Little JW, Harper JE. Identification of the lexA gene product of Escherichia coli K-12. Proc. Nat. Acad. Sci. USA 76(12) (1979), p. 6147-6151.
29- Little JW, Edmiston SH, Pacelli LZ, Mount DW. Cleavage of the Escherichia coli LexA protein by the RecA protease. Proc. Nat. Acad. Sci. USA 77(6) (1980), p. 3225-3329.
30- Little JW, Mount DW, Yanis-Perron CR. Purified LexA protein is a repressor of the recA and lexA genes. Proc. Nat. Acad. Sci. USA 78(7) (1981), p. 4199-4203.
31- Brent R, Ptashne M. Mechanism of action of the lexA gene product. Proc. Nat. Acad. Sci. USA 78(7) (1981), p. 4204-4208
32- Little JW Autodigestion of LexA and phage λ repressors. Proc. Nat. Acad. Sci. USA 81 (3) (1984), p. 1375-1379.
33- Bailone A, Brandenburger A, Lévine A, Pierre M, Dutreix M, Devoret R. Indirect SOS induction is promoted by ultraviolet light-damaged miniF and requires the miniF lynA locus. J. Mol. Biol. 179(3) (1984), p. 367-390.
34- Brandenburger A, Bailone A, Lévine A, Devoret R. Gratuitous induction. J. Mol. Biol. 179(3) (1984), p. 571-576.
35- Sommer S, Bailone A, Devoret R. SOS induction by thermosensitive replication mutants of miniF plasmid. Mol. Gen. Genet. 198(3) (1985), p. 456-464.
36- Bailone A, Sommer S, Devoret R. Mini-F plasmid-induced SOS signal in Escherichia coli is RecBC dependent. Proc. Natl. Acad. Sci. USA. 82(17) (1985), p. 5973-5977.
37- Bernard P, Couturier M. Cell killing by the F plasmid CcdB protein involves poisoning of DNA-topoisomerase II complexes. J. Mol. Biol. 226(3) (1992), p. 735-745.
38- Bernard P, Kézdy KE, Van Melderen L, Steyaert J, Wyns L, Pato ML, Higgins PN, Couturier M. The F plasmid CcdB protein induces efficient ATP-dependent DNA cleavage by gyrase. J. Mol. Biol. 234(3) (1993), p. 534-541.
39- Sommer S, Knezević J, Bailone A, Devoret R. Induction of only one SOS operon, umuDC, is required for SOS mutagenesis in Escherichia coli. Mol. Gen. Genet. 239 (1993), p. 137-144.
40- Sommer S, Bailone A, Devoret R. The appearance of the UmuD'C protein complex in Escherichia coli switches repair from homologous recombination to SOS mutagenesis. Mol. Microbiol. 10(5) (1993), p. 963-971.
41- Szpilewska H, Bertrand P, Bailone A, Dutreix M. In vitro inhibition of RecA-mediated homologous pairing by UmuD'C proteins. Biochimie 77 (11) (1995), p. 848-853.
42- Boudsocq F, Campbell M, Devoret R, Bailone A. Quantitation of the inhibition of Hfr x F- recombination by the mutagenesis complex UmuD'C. J. Mol. Biol. 270(2) (1997), p. 201-211.
43- Bailone A, Sommer S, Knezević J, Dutreix M, Devoret R. A RecA protein mutant deficient in its interaction with the UmuDC complex. Biochimie 73(4) (1991), p. 479-484.
44- Dutreix M, Moreau PL, Bailone A, Galibert F, Battista JR, Walker GC, Devoret R. New recA mutations that dissociate the various RecA protein activities in Escherichia coli provide evidence for an additional role for RecA protein in UV mutagenesis, J. Bacteriol. 171 (5) (1989) p. 2415-2423.
45- Dutreix M, Burnett B, Bailone A, Radding CM, Devoret R. A partially deficient mutant, recA1730, that fails to form normal nucleoprotein filaments. Mol. Gen. Genet. 232(3) (1992), p. 489-497.
46- Sommer S, Boudsocq F, Devoret R, Bailone A. Specific RecA amino acid changes affect RecA-UmuD'C interaction. Mol. Microbiol. 28(2) (1998), p. 281-291.
47- Reuven NB, Arad G, Maor-Shoshani A, Livneh Z. The mutagenesis protein UmuC is a DNA polymerase activated by UmuD', RecA, and SSB and is specialized for translesion replication. J. Biol. Chem. 274(45) (1999), p. 31763-37766.
48- Tang M, Shen X, Frank EG, O’Donnell M, Woodgate R, Goodman MF. UmuD'(2)C is an error-prone DNA polymerase, Escherichia coli Pol V. Proc. Nat. Acad. Sci. USA 96(16) (1999), p. 8919-8924.
49- Ohmori H, Friedberg EC, Fuchs RP, Goodman MF, Hanaoka F, Hinkle D, Kunkel TA, Lawrence CW, Livneh Z, Nohmi T, Prakash L, Prakash S, Todo T, Walker GC, Wang Z, Woodgate R. The Y family of DNA polymerases. Mol Cell. 8 (2001), p. 7-8.
50- Zahradka K, Slade D, Bailone A, Sommer S, Averbeck D, Petranovic M, Lindner AB, Radman M. Reassembly of shattered chromosomes in Deinococcus radiodurans. Nature 443(7111) (2006), p. 569-573.
51- Bouthier de la Tour C, Boisnard S, Norais C, Toueille M, Bentchikou E, Vannier F, Cox MM, Sommer S, Servant P. The deinococcal DdrB protein is involved in an early step of DNA double strand break repair and in plasmid transformation through its single-strand annealing activity. DNA repair 10(12) (2011), p. 1223-1231.
52- Devigne A, Ithurbide S, Bouthier de la Tour C, Passot F, Mathieu M, Sommer S, Servant P. DdrO is an essential protein that regulates the radiation desiccation response and the apoptotic-like cell death in the radioresistant Deinococcus radiodurans bacterium. Mol Microbiol 96(5) (2015), p. 1069-1084.
53- Meyer L, Coste G, Sommer S, Oberto J, Confalonieri F, Servant P, Pasternak C. DdrI, a cAMP Receptor Protein Family Member, Acts as a Major Regulator for Adaptation of Deinococcus radiodurans to Various Stresses. J Bacteriol. 200(13) (2018), e00129-18.
54- Pasternak C, Ton-Hoang B, Coste G, Bailone A, Chandler M, Sommer S. Irradiation-induced Deinococcus radiodurans genome fragmentation triggers transposition of a single resident insertion sequence. PLoS Genet. 6(1) (2010), e1000799.
55- Ton-Hoang B,Pasternak C, Siguier P, Guynet C, Hickman AB, Dyda F, Sommer S, Chandler. Single-stranded DNA transposition is coupled to host replication. Cell 142(3) (2010), p. 398-408.
56- Daly MJ, Gaidamakova EK, Matrosova VY, Vasilenko A, Zhai M, Leapman RD, Lai B, Ravel B, Li SMW, Kemner KM, Fredrickson JK. Protein oxidation implicated as the primary determinant of bacterial radioresistance. PLoS Biol. 5(4) (2007), e92.
57- Daly MJ. A new perspective on radiation resistance based on Deinococcus radiodurans. Nat. Rev. Microbiol. 7(3) (2009), p. 237-245.
58- Slade D, Radman M. Oxidative stress resistance in Deinococcus radiodurans. Microbiol. Mol. Biol. Rev. 75(1) (2011), p. 133-191.
59- Benoit I, Burty-Valin E, Radman M. A Proteome-Centric View of Ageing, including that of the Skin and Age-Related Diseases : Considerations of a Common Cause and Common Preventative and Curative Interventions. Clin Cosmet Investig Dermatol. 16 (2023), p. 79-85.

















