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ISSN 1214-0287 (on-line), ISSN 1214-021X (printed)
J Appl Biomed
Volume 8 (2010), No 3, p 151-158
DOI 10.2478/v10136-009-0018-4

Voyage of RepA protein from plasmid DNA replication through amyloid aggregation towards synthetic biology

Rafael Giraldo, Maria Elena Fernandez-Tresguerres

Address: Rafael Giraldo, Department of Chemical and Physical Biology, Centro de Investigaciones Biologicas (CIB) - CSIC, Ramiro de Maeztu 9, E-28040 Madrid, Spain
rgiraldo@cib.csic.es

Received 1st March 2010.
Revised 12th April 2010.
Published online 12th May 2010.

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SUMMARY
DNA replication of plasmids in Gram-negative bacteria has been an object of study at CIB-CSIC for nearly 30 years. We have been focused on the enterobacterial antibiotic resistance factor R1 (1981-1992) and the pPS10 replicon from the phytopathogen Pseudomonas savastanoi (since 1984). Our group has used multidisciplinary (genetic, biochemical and biophysical-structural) approaches to unravel the molecular mechanism for the activation of RepA. Rep-type plasmidic proteins are either transcriptional repressors or replication initiators/inhibitors, depending on their association state (dimers vs. monomers) and targeting of alternative (operator or iteron) DNA sites. We discovered that allosteric DNA-binding remodels the structure of RepA N-terminal domain (WH1), transforming alpha-helical portions into beta-strands. This precisely tunes the distances between the DNA reading heads in WH1 and the C-terminal domain (WH2), to match the target operator or iteron sequences. We have recently moved into engineering such structural transformation in RepA-WH1 to build-up synthetic protein devices that allow for customized ligand (DNA)-promoted amyloidogenesis. Our basic studies on plasmid DNA replication are relevant for settling the bases of a minimalist bacterial model to tackle transmissible amyloid proteinopathies and are a valuable tool for bottom-up synthetic biology.

KEY WORDS
plasmid replication; protein amyloids; protein-DNA interactions; RepA protein; synthetic biology

REFERENCES
Bell SP: The origin recognition complex: from simple origins to complex functions. Genes Dev 16:659-672, 2002.

Chiti F, Dobson CM: Protein misfolding, functional amyloid, and human disease. Annu Rev Biochem 75:333-366, 2006.

del Solar G, Giraldo R, Ruiz-Echevarria MJ, Espinosa M, Diaz R: Replication and control of circular bacterial plasmids. Microbiol Mol Biol Rev 62:434-464, 1998.

Diaz R, Ortega S: Initiation of plasmid R1 replication in vitro is dependent of transcription by host RNA polymerase. Nucleic Acids Res 12:5175-5191, 1984.

Diaz R, Nordstrom K, Staudenbauer WL: Plasmid R1 DNA replication dependent on protein synthesis in cell-free extracts of E. coli. Nature 289:326-328, 1981.

Diaz-Lopez T, Lages-Gonzalo M, Serrano-Lopez A, Alfonso C, Rivas G, Diaz-Orejas R, Giraldo R: Structural changes in RepA, a plasmid replication initiator, upon binding to origin DNA. J Biol Chem 278:18606-18616, 2003.

Diaz-Lopez T, Davila-Fajardo C, Blaesing F, Lillo MP, Giraldo R: Early events in the binding of the pPS10 replication protein RepA to single iteron and operator DNA sequences. J Mol Biol 364:909-920, 2006.

Diederix REM, Davila-Fajardo C, Giraldo R, Lillo MP: Fluorescence studies of the replication initiator protein RepA in complex with operator and iteron sequences and free in solution. FEBS J 275:5393-5407, 2008.

Fernandez-Tresguerres ME, Martin M, Garcia de Viedma D, Giraldo R, Diaz-Orejas R: Host growth temperature and a conservative amino acid substitution in the replication protein of pPS10 plasmid influence plasmid host range. J Bacteriol 177:4377-4384, 1995.

Garcia de Viedma D, Giraldo R, Ruiz-Echevarria MJ, Lurz R, Diaz-Orejas R: Transcription of repA, the gene of the initiation protein of the Pseudomonas plasmid pPS10, is autorregulated by interactions of the RepA protein at a symmetrical operator. J Mol Biol 247:211-223, 1995a.

Garcia de Viedma D, Serrano-Lopez A, Diaz-Orejas R: Specific binding of the replication protein of plasmid pPS10 to direct and inverted repeats is mediated by an HTH motif. Nucleic Acids Res 23:5048-5054, 1995b.

Garcia de Viedma D, Giraldo R, Rivas G, Fernandez-Tresguerres E, Diaz-Orejas R: A Leucine-Zipper motif determines different functions in a DNA replication protein. EMBO J 15:925-934, 1996.

Gasset-Rosa F, Diaz-Lopez T, Lurz R, Prieto A, Fernandez-Tresguerres ME, Giraldo R: Negative regulation of pPS10 plasmid replication: Origin pairing by zipping-up DNA-bound RepA monomers. Mol Microbiol 68:560-572, 2008a.

Gasset-Rosa F, Mate MJ, Davila-Fajardo C, Bravo J, Giraldo R: Binding of sulphonated indigo derivatives to RepA-WH1 inhibits DNA-induced protein amyloidogenesis. Nucleic Acids Res 36:2249-2256, 2008b.

Giraldo R: Common domains in the initiators of DNA replication in Bacteria, Archaea and Eukarya: Combined structural, functional and phylogenetic perspectives. FEMS Microbiol Rev 26:533-554, 2003.

Giraldo R: Defined DNA sequences promote de assembly of a bacterial protein into distinct amyloid nanostructures. Proc Natl Acad Sci USA 104:17388-17393, 2007.

Giraldo R, Diaz R: Differential binding of wild-type and a mutant RepA protein to oriR sequence suggests a model for the initiation of plasmid R1 replication. J Mol Biol 228:787-802, 1992.

Giraldo R, Diaz-Orejas R: Similarities between the DNA replication initiators of Gram-negative bacteria plasmids (RepA) and eukaryotes (Orc4p) / archaea (Cdc6p). Proc Natl Acad Sci USA 98:4938-4943, 2001.

Giraldo R, Nieto C, Fernandez-Tresguerres ME, Diaz R: Bacterial zipper. Nature 342:866, 1989.

Giraldo R, Martin M, Fernandez-Tresguerres ME, Nieto C, Diaz R: Mutations within the minimal replicon of plasmid pPS10 increase its host range. In Hughes P, Fanning E, Kohiyama M (eds.): DNA Replication: The Regulatory Mechanisms, Springer Verlag, Berlin, 1992, pp. 225-237.

Giraldo R, Andreu JM, Diaz-Orejas R: Protein domains and conformational changes in the activation of RepA, a DNA replication initiator. EMBO J 17:4511-4526, 1998.

Giraldo R, Fernandez-Tornero C, Evans PR, Diaz-Orejas R, Romero A: A conformational switch between transcriptional repression and replication initiation in the RepA dimerization domain. Nat Struct Biol 10:565-571, 2003.

Giraldo R, Fernandez-Tresguerres ME: 20 years of the pPS10 replicon: Insights on the molecular mechanism for the activation of DNA replication in iteron-containing bacterial plasmids. Plasmid 52:69-83, 2004.

Giraldo-Suarez R, Fernandez-Tresguerres ME, Diaz-Orejas R, Malki A, Kohiyama M: The heat-shock DnaK protein is required for plasmid R1 replication and it is dispensable for plasmid ColE1 replication. Nucleic Acids Res 21:5495-5499, 1993.

Grabowski B, Kelman Z: Archaeal DNA replication: Eukaryal proteins in a bacterial context. Annu Rev Microbiol 57:467-485, 2003.

Komori H, Matsunaga F, Higuchi Y, Ishiai M, Wada C, Miki K: Crystal structure of a prokaryotic replication initiator protein bound to DNA at 2.6A resolution. EMBO J 18:4597-4607, 1999.

Kruger R, Rakowski SA, Filutowicz M: Participating elements in the replication of iteron containing plasmids. In Funnell BE, Phillips GJ (eds.): Plasmid Biology, ASM Press, Washington DC, 2004, pp 25-45.

Liu J, Smith CL, DeRyckere D, DeAngelis K, Martin GS, Berger JM: Structure and function of Cdc6/Cdc18: Implications for origin recognition and checkpoint control. Mol Cell 6:637-648, 2000.

Maestro B, Sanz JM, Faelen M, Couturier M, Diaz-Orejas R, Fernandez-Tresguerres ME: Modulation of pPS10 host range by DnaA. Mol Microbiol 46:223-234, 2002.

Maestro B, Sanz JM, Diaz-Orejas R, Fernandez-Tresguerres E: Modulation of pPS10 host range by plasmid-encoded RepA initiator protein. J Bacteriol 185:1367-1375, 2003.

Nakamura A, Wada C, Miki K: Structural basis for regulation of bifunctional roles in replication initiator protein. Proc Natl Acad Sci USA 104:18484-18489, 2007.

Nieto C, Fernandez-Tresguerres E, Sanchez N, Vicente M, Diaz R: Cloning vectors, derived from a naturally occurring plasmid of Pseudomonas savastanoi, specifically tailored for genetic manipulations in Pseudomonas. Gene 87:145-149, 1990.

Nieto C, Giraldo R, Fernandez-Tresguerres E, Diaz R: Genetic and functional analysis of the basic replicon of pPS10, a plasmid specific of Pseudomonas isolated from Pseudomonas syringae pv. savastanoi. J Mol Biol 223:415-426, 1992.

Ortega S, Lanka E, Diaz R: The involvement of host replication proteins and of specific origin sequences in the in vitro replication of miniplasmid R1 DNA. Nucleic Acids Res 14:428-435, 1986.

Ortega-Jimenez S, Giraldo-Suarez R, Fernandez-Tresguerres ME, Berzal-Herranz A, Diaz-Orejas R: DnaA-dependent replication of plasmid R1 occurs in the presence of point mutations that disrupt the dnaA box of oriR. Nucleic Acids Res 20:2547-2551, 1992.

Paulsson J, Chattoraj DK: Origin inactivation in bacterial DNA replication control. Mol Microbiol 61:9-15, 2006.

Tresguerres EF, Nandadasa HG, Pritchard RH: Suppression of initiation negative strains of Escherichia coli by integration of the sex factor F. J Bacteriol 121:554-561, 1975.

Wickner S, Hoskins J, McKenney K: Function of DnaJ and DnaK chaperones in origin-specific DNA binding by RepA. Nature 350:165-167, 1991.
CITED

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