Abstract
Traditionally, new loci involved in the Rhizobium-legume symbiosis have been identified by transposon mutagenesis and/or complementation. Wide dispersal of the symbiotic loci in Rhizobium species NGR234, as well as the large number of potential host-plants to be screened, greatly reduces the efficiency of these techniques. As an alternate strategy designed to identify new NGR234 genes involved in the early stages of the symbiosis, we combined data from competitive RNA hybridisation, subtractive DNA hybridisation and shot-gun sequencing. On the assumption that the expression of most nodulation genes is triggered by compounds released by the host-plant, we identified, in the ordered cosmid library of the large symbiotic plasmid pNGR234a, restriction fragments that carry transcripts induced by flavonoids. To target genes not present in the closely related strain R. fredii USDA257, we selected fragments that also carried sequences purified by subtractive DNA hybridisation. Shot-gun sequencing of this subset of fragments lead to the identification of sequences with strong homology to diverse prokaryotic genes/proteins. Amongst these, a symbiotically active ORF from pNGR234a, is highly homologous to the leucine responsive regulatory protein of Escherichia coli (Lrp), is induced by flavonoids, and is not present in USDA257.
Full text
PDF






Images in this article
Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Alley M. R., Maddock J. R., Shapiro L. Polar localization of a bacterial chemoreceptor. Genes Dev. 1992 May;6(5):825–836. doi: 10.1101/gad.6.5.825. [DOI] [PubMed] [Google Scholar]
- Altschul S. F., Gish W., Miller W., Myers E. W., Lipman D. J. Basic local alignment search tool. J Mol Biol. 1990 Oct 5;215(3):403–410. doi: 10.1016/S0022-2836(05)80360-2. [DOI] [PubMed] [Google Scholar]
- Bjourson A. J., Stone C. E., Cooper J. E. Combined subtraction hybridization and polymerase chain reaction amplification procedure for isolation of strain-specific Rhizobium DNA sequences. Appl Environ Microbiol. 1992 Jul;58(7):2296–2301. doi: 10.1128/aem.58.7.2296-2301.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Brenner S., Elgar G., Sandford R., Macrae A., Venkatesh B., Aparicio S. Characterization of the pufferfish (Fugu) genome as a compact model vertebrate genome. Nature. 1993 Nov 18;366(6452):265–268. doi: 10.1038/366265a0. [DOI] [PubMed] [Google Scholar]
- Broughton W. J., Wong C. H., Lewin A., Samrey U., Myint H., Meyer H., Dowling D. N., Simon R. Identification of Rhizobium plasmid sequences involved in recognition of Psophocarpus, Vigna, and other legumes. J Cell Biol. 1986 Apr;102(4):1173–1182. doi: 10.1083/jcb.102.4.1173. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Cami B., Kourilsky P. Screening of cloned recombinant DNA in bacteria by in situ colony hybridization. Nucleic Acids Res. 1978 Jul;5(7):2381–2390. doi: 10.1093/nar/5.7.2381. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Figurski D. H., Helinski D. R. Replication of an origin-containing derivative of plasmid RK2 dependent on a plasmid function provided in trans. Proc Natl Acad Sci U S A. 1979 Apr;76(4):1648–1652. doi: 10.1073/pnas.76.4.1648. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Griffin A. M. Identification of 21 genes of infectious laryngotracheitis virus using random sequencing of genomic DNA. J Gen Virol. 1989 Nov;70(Pt 11):3085–3089. doi: 10.1099/0022-1317-70-11-3085. [DOI] [PubMed] [Google Scholar]
- Göttfert M., Grob P., Hennecke H. Proposed regulatory pathway encoded by the nodV and nodW genes, determinants of host specificity in Bradyrhizobium japonicum. Proc Natl Acad Sci U S A. 1990 Apr;87(7):2680–2684. doi: 10.1073/pnas.87.7.2680. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hanahan D. Studies on transformation of Escherichia coli with plasmids. J Mol Biol. 1983 Jun 5;166(4):557–580. doi: 10.1016/s0022-2836(83)80284-8. [DOI] [PubMed] [Google Scholar]
- Heron D. S., Pueppke S. G. Mode of infection, nodulation specificity, and indigenous plasmids of 11 fast-growing Rhizobium japonicum strains. J Bacteriol. 1984 Dec;160(3):1061–1066. doi: 10.1128/jb.160.3.1061-1066.1984. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Higgins D. G., Sharp P. M. CLUSTAL: a package for performing multiple sequence alignment on a microcomputer. Gene. 1988 Dec 15;73(1):237–244. doi: 10.1016/0378-1119(88)90330-7. [DOI] [PubMed] [Google Scholar]
- Kahn D., David M., Domergue O., Daveran M. L., Ghai J., Hirsch P. R., Batut J. Rhizobium meliloti fixGHI sequence predicts involvement of a specific cation pump in symbiotic nitrogen fixation. J Bacteriol. 1989 Feb;171(2):929–939. doi: 10.1128/jb.171.2.929-939.1989. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Kehry M. R., Bond M. W., Hunkapiller M. W., Dahlquist F. W. Enzymatic deamidation of methyl-accepting chemotaxis proteins in Escherichia coli catalyzed by the cheB gene product. Proc Natl Acad Sci U S A. 1983 Jun;80(12):3599–3603. doi: 10.1073/pnas.80.12.3599. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Krishnan H. B., Lewin A., Fellay R., Broughton W. J., Pueppke S. G. Differential expression of nodS accounts for the varied abilities of Rhizobium fredii USDA257 and Rhizobium sp. strain NGR234 to nodulate Leucaena spp. Mol Microbiol. 1992 Nov;6(22):3321–3330. doi: 10.1111/j.1365-2958.1992.tb02200.x. [DOI] [PubMed] [Google Scholar]
- Lewin A., Cervantes E., Chee-Hoong W., Broughton W. J. nodSU, two new nod genes of the broad host range Rhizobium strain NGR234 encode host-specific nodulation of the tropical tree Leucaena leucocephala. Mol Plant Microbe Interact. 1990 Sep-Oct;3(5):317–326. doi: 10.1094/mpmi-3-317. [DOI] [PubMed] [Google Scholar]
- Madhusudhan K. T., Lorenz D., Sokatch J. R. The bkdR gene of Pseudomonas putida is required for expression of the bkd operon and encodes a protein related to Lrp of Escherichia coli. J Bacteriol. 1993 Jul;175(13):3934–3940. doi: 10.1128/jb.175.13.3934-3940.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Morrison N. A., Hau C. Y., Trinick M. J., Shine J., Rolfe B. G. Heat curing of a sym plasmid in a fast-growing Rhizobium sp. that is able to nodulate legumes and the nonlegume Parasponia sp. J Bacteriol. 1983 Jan;153(1):527–531. doi: 10.1128/jb.153.1.527-531.1983. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Newman E. B., D'Ari R., Lin R. T. The leucine-Lrp regulon in E. coli: a global response in search of a raison d'être. Cell. 1992 Feb 21;68(4):617–619. doi: 10.1016/0092-8674(92)90135-y. [DOI] [PubMed] [Google Scholar]
- Nucifora G., Chu L., Misra T. K., Silver S. Cadmium resistance from Staphylococcus aureus plasmid pI258 cadA gene results from a cadmium-efflux ATPase. Proc Natl Acad Sci U S A. 1989 May;86(10):3544–3548. doi: 10.1073/pnas.86.10.3544. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Overduin P., Boos W., Tommassen J. Nucleotide sequence of the ugp genes of Escherichia coli K-12: homology to the maltose system. Mol Microbiol. 1988 Nov;2(6):767–775. doi: 10.1111/j.1365-2958.1988.tb00088.x. [DOI] [PubMed] [Google Scholar]
- Parsons J. D., Brenner S., Bishop M. J. Clustering cDNA sequences. Comput Appl Biosci. 1992 Oct;8(5):461–466. doi: 10.1093/bioinformatics/8.5.461. [DOI] [PubMed] [Google Scholar]
- Paulus F., Canaday J., Vincent F., Bonnard G., Kares C., Otten L. Sequence of the iaa and ipt region of different Agrobacterium tumefaciens biotype III octopine strains: reconstruction of octopine Ti plasmid evolution. Plant Mol Biol. 1991 Apr;16(4):601–614. doi: 10.1007/BF00023425. [DOI] [PubMed] [Google Scholar]
- Perret X., Broughton W. J., Brenner S. Canonical ordered cosmid library of the symbiotic plasmid of Rhizobium species NGR234. Proc Natl Acad Sci U S A. 1991 Mar 1;88(5):1923–1927. doi: 10.1073/pnas.88.5.1923. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Peterson S. N., Schramm N., Hu P. C., Bott K. F., Hutchison C. A., 3rd A random sequencing approach for placing markers on the physical map of Mycoplasma genitalium. Nucleic Acids Res. 1991 Nov 11;19(21):6027–6031. doi: 10.1093/nar/19.21.6027. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Platko J. V., Calvo J. M. Mutations affecting the ability of Escherichia coli Lrp to bind DNA, activate transcription, or respond to leucine. J Bacteriol. 1993 Feb;175(4):1110–1117. doi: 10.1128/jb.175.4.1110-1117.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Prentki P., Krisch H. M. In vitro insertional mutagenesis with a selectable DNA fragment. Gene. 1984 Sep;29(3):303–313. doi: 10.1016/0378-1119(84)90059-3. [DOI] [PubMed] [Google Scholar]
- Quandt J., Hynes M. F. Versatile suicide vectors which allow direct selection for gene replacement in gram-negative bacteria. Gene. 1993 May 15;127(1):15–21. doi: 10.1016/0378-1119(93)90611-6. [DOI] [PubMed] [Google Scholar]
- Sanger F., Nicklen S., Coulson A. R. DNA sequencing with chain-terminating inhibitors. Proc Natl Acad Sci U S A. 1977 Dec;74(12):5463–5467. doi: 10.1073/pnas.74.12.5463. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Willins D. A., Ryan C. W., Platko J. V., Calvo J. M. Characterization of Lrp, and Escherichia coli regulatory protein that mediates a global response to leucine. J Biol Chem. 1991 Jun 15;266(17):10768–10774. [PubMed] [Google Scholar]
- de Maagd R. A., Mulders I. H., Canter Cremers H. C., Lugtenberg B. J. Cloning, nucleotide sequencing, and expression in Escherichia coli of a Rhizobium leguminosarum gene encoding a symbiotically repressed outer membrane protein. J Bacteriol. 1992 Jan;174(1):214–221. doi: 10.1128/jb.174.1.214-221.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]