Abstract
Anonymous probes from the genome of Halobacterium salinarium GRB and 12 gene probes were hybridized to the cosmid clones representing the chromosome and plasmids of Halobacterium salinarium GRB and Haloferax volcanii DS2. The order of and pairwise distances between 35 loci uniquely cross-hybridizing to both chromosomes were analyzed in a search for conservation. No conservation between the genomes could be detected at the 15-kbp resolution used in this study. We found distinct sets of low-copy-number repeated sequences in the chromosome and plasmids of Halobacterium salinarium GRB, indicating some degree of partitioning between these replicons. We propose alternative courses for the evolution of the haloarchaeal genome: (i) that the majority of genomic differences that exist between genera came about at the inception of this group or (ii) that the differences have accumulated over the lifetime of the lineage. The strengths and limitations of investigating these models through comparative genomic studies are discussed.
Full Text
The Full Text of this article is available as a PDF (622.9 KB).
Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Canard B., Saint-Joanis B., Cole S. T. Genomic diversity and organization of virulence genes in the pathogenic anaerobe Clostridium perfringens. Mol Microbiol. 1992 Jun;6(11):1421–1429. doi: 10.1111/j.1365-2958.1992.tb00862.x. [DOI] [PubMed] [Google Scholar]
- Carlson C. R., Grønstad A., Kolstø A. B. Physical maps of the genomes of three Bacillus cereus strains. J Bacteriol. 1992 Jun;174(11):3750–3756. doi: 10.1128/jb.174.11.3750-3756.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Carlson C. R., Kolstø A. B. A complete physical map of a Bacillus thuringiensis chromosome. J Bacteriol. 1993 Feb;175(4):1053–1060. doi: 10.1128/jb.175.4.1053-1060.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Casjens S., Delange M., Ley H. L., 3rd, Rosa P., Huang W. M. Linear chromosomes of Lyme disease agent spirochetes: genetic diversity and conservation of gene order. J Bacteriol. 1995 May;177(10):2769–2780. doi: 10.1128/jb.177.10.2769-2780.1995. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Charlebois R. L., Schalkwyk L. C., Hofman J. D., Doolittle W. F. Detailed physical map and set of overlapping clones covering the genome of the archaebacterium Haloferax volcanii DS2. J Mol Biol. 1991 Dec 5;222(3):509–524. doi: 10.1016/0022-2836(91)90493-p. [DOI] [PubMed] [Google Scholar]
- Charlebois R. L., St Jean A. Supercoiling and map stability in the bacterial chromosome. J Mol Evol. 1995 Jul;41(1):15–23. doi: 10.1007/BF00174037. [DOI] [PubMed] [Google Scholar]
- Cohen A., Lam W. L., Charlebois R. L., Doolittle W. F., Schalkwyk L. C. Localizing genes on the map of the genome of Haloferax volcanii, one of the Archaea. Proc Natl Acad Sci U S A. 1992 Mar 1;89(5):1602–1606. doi: 10.1073/pnas.89.5.1602. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Cole S. T., Saint Girons I. Bacterial genomics. FEMS Microbiol Rev. 1994 Jun;14(2):139–160. doi: 10.1111/j.1574-6976.1994.tb00084.x. [DOI] [PubMed] [Google Scholar]
- DasSarma S. Mechanisms of genetic variability in Halobacterium halobium: the purple membrane and gas vesicle mutations. Can J Microbiol. 1989 Jan;35(1):65–72. doi: 10.1139/m89-010. [DOI] [PubMed] [Google Scholar]
- Fonstein M., Haselkorn R. Physical mapping of bacterial genomes. J Bacteriol. 1995 Jun;177(12):3361–3369. doi: 10.1128/jb.177.12.3361-3369.1995. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Fonstein M., Nikolskaya T., Haselkorn R. High-resolution alignment of a 1-megabase-long genome region of three strains of Rhodobacter capsulatus. J Bacteriol. 1995 May;177(9):2368–2372. doi: 10.1128/jb.177.9.2368-2372.1995. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Gerl L., Sumper M. Halobacterial flagellins are encoded by a multigene family. Characterization of five flagellin genes. J Biol Chem. 1988 Sep 15;263(26):13246–13251. [PubMed] [Google Scholar]
- Grothues D., Tümmler B. New approaches in genome analysis by pulsed-field gel electrophoresis: application to the analysis of Pseudomonas species. Mol Microbiol. 1991 Nov;5(11):2763–2776. doi: 10.1111/j.1365-2958.1991.tb01985.x. [DOI] [PubMed] [Google Scholar]
- Hackett N. R., Bobovnikova Y., Heyrovska N. Conservation of chromosomal arrangement among three strains of the genetically unstable archaeon Halobacterium salinarium. J Bacteriol. 1994 Dec;176(24):7711–7718. doi: 10.1128/jb.176.24.7711-7718.1994. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hofman J. D., Schalkwyk L. C., Doolittle W. F. ISH51: a large, degenerate family of insertion sequence-like elements in the genome of the archaebacterium, Halobacterium volcanii. Nucleic Acids Res. 1986 Sep 11;14(17):6983–7000. doi: 10.1093/nar/14.17.6983. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Horne M., Englert C., Pfeifer F. Two genes encoding gas vacuole proteins in Halobacterium halobium. Mol Gen Genet. 1988 Aug;213(2-3):459–464. doi: 10.1007/BF00339616. [DOI] [PubMed] [Google Scholar]
- Joshi P., Dennis P. P. Characterization of paralogous and orthologous members of the superoxide dismutase gene family from genera of the halophilic archaebacteria. J Bacteriol. 1993 Mar;175(6):1561–1571. doi: 10.1128/jb.175.6.1561-1571.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Krawiec S., Riley M. Organization of the bacterial chromosome. Microbiol Rev. 1990 Dec;54(4):502–539. doi: 10.1128/mr.54.4.502-539.1990. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Ladefoged S. A., Christiansen G. Physical and genetic mapping of the genomes of five Mycoplasma hominis strains by pulsed-field gel electrophoresis. J Bacteriol. 1992 Apr;174(7):2199–2207. doi: 10.1128/jb.174.7.2199-2207.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Le Bourgeois P., Lautier M., van den Berghe L., Gasson M. J., Ritzenthaler P. Physical and genetic map of the Lactococcus lactis subsp. cremoris MG1363 chromosome: comparison with that of Lactococcus lactis subsp. lactis IL 1403 reveals a large genome inversion. J Bacteriol. 1995 May;177(10):2840–2850. doi: 10.1128/jb.177.10.2840-2850.1995. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Leblond P., Redenbach M., Cullum J. Physical map of the Streptomyces lividans 66 genome and comparison with that of the related strain Streptomyces coelicolor A3(2). J Bacteriol. 1993 Jun;175(11):3422–3429. doi: 10.1128/jb.175.11.3422-3429.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Liu S. L., Sanderson K. E. Rearrangements in the genome of the bacterium Salmonella typhi. Proc Natl Acad Sci U S A. 1995 Feb 14;92(4):1018–1022. doi: 10.1073/pnas.92.4.1018. [DOI] [PMC free article] [PubMed] [Google Scholar]
- López-García P., Abad J. P., Smith C., Amils R. Genomic organization of the halophilic archaeon Haloferax mediterranei: physical map of the chromosome. Nucleic Acids Res. 1992 May 25;20(10):2459–2464. doi: 10.1093/nar/20.10.2459. [DOI] [PMC free article] [PubMed] [Google Scholar]
- López-García P., St Jean A., Amils R., Charlebois R. L. Genomic stability in the archaeae Haloferax volcanii and Haloferax mediterranei. J Bacteriol. 1995 Mar;177(5):1405–1408. doi: 10.1128/jb.177.5.1405-1408.1995. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Lück P. C., Helbig J. H., Drasar V., Bornstein N., Fallon R. J., Castellani-Pastoris M. Genomic heterogenicity amongst phenotypically similar Legionella micdadei strains. FEMS Microbiol Lett. 1995 Feb 1;126(1):49–54. doi: 10.1111/j.1574-6968.1995.tb07389.x. [DOI] [PubMed] [Google Scholar]
- Mankin A. S., Kagramanova V. K., Teterina N. L., Rubtsov P. M., Belova E. N., Kopylov A. M., Baratova L. A., Bogdanov A. A. The nucleotide sequence of the gene coding for the 16S rRNA from the archaebacterium Halobacterium halobium. Gene. 1985;37(1-3):181–189. doi: 10.1016/0378-1119(85)90271-9. [DOI] [PubMed] [Google Scholar]
- Mojica F. J., Ferrer C., Juez G., Rodríguez-Valera F. Long stretches of short tandem repeats are present in the largest replicons of the Archaea Haloferax mediterranei and Haloferax volcanii and could be involved in replicon partitioning. Mol Microbiol. 1995 Jul;17(1):85–93. doi: 10.1111/j.1365-2958.1995.mmi_17010085.x. [DOI] [PubMed] [Google Scholar]
- Ochman H., Wilson A. C. Evolution in bacteria: evidence for a universal substitution rate in cellular genomes. J Mol Evol. 1987;26(1-2):74–86. doi: 10.1007/BF02111283. [DOI] [PubMed] [Google Scholar]
- Ojaimi C., Davidson B. E., Saint Girons I., Old I. G. Conservation of gene arrangement and an unusual organization of rRNA genes in the linear chromosomes of the Lyme disease spirochaetes Borrelia burgdorferi, B. garinii and B. afzelii. Microbiology. 1994 Nov;140(Pt 11):2931–2940. doi: 10.1099/13500872-140-11-2931. [DOI] [PubMed] [Google Scholar]
- Peterson S. N., Lucier T., Heitzman K., Smith E. A., Bott K. F., Hu P. C., Hutchison C. A., 3rd Genetic map of the Mycoplasma genitalium chromosome. J Bacteriol. 1995 Jun;177(11):3199–3204. doi: 10.1128/jb.177.11.3199-3204.1995. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Pfeifer F., Betlach M. Genome organization in Halobacterium halobium: a 70 kb island of more (AT) rich DNA in the chromosome. Mol Gen Genet. 1985;198(3):449–455. doi: 10.1007/BF00332938. [DOI] [PubMed] [Google Scholar]
- Pfeifer F., Blaseio U. Transposition burst of the ISH27 insertion element family in Halobacterium halobium. Nucleic Acids Res. 1990 Dec 11;18(23):6921–6925. doi: 10.1093/nar/18.23.6921. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Sanz J. L., Marín I., Ramirez L., Abad J. P., Smith C. L., Amils R. Variable rRNA gene copies in extreme halobacteria. Nucleic Acids Res. 1988 Aug 25;16(16):7827–7832. doi: 10.1093/nar/16.16.7827. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Sapienza C., Doolittle W. F. Unusual physical organization of the Halobacterium genome. Nature. 1982 Feb 4;295(5848):384–389. doi: 10.1038/295384a0. [DOI] [PubMed] [Google Scholar]
- Sapienza C., Rose M. R., Doolittle W. F. High-frequency genomic rearrangements involving archaebacterial repeat sequence elements. Nature. 1982 Sep 9;299(5879):182–185. doi: 10.1038/299182a0. [DOI] [PubMed] [Google Scholar]
- Soppa J., Oesterhelt D. Halobacterium sp. GRB: a species to work with!? Can J Microbiol. 1989 Jan;35(1):205–209. doi: 10.1139/m89-032. [DOI] [PubMed] [Google Scholar]
- St Jean A., Trieselmann B. A., Charlebois R. L. Physical map and set of overlapping cosmid clones representing the genome of the archaeon Halobacterium sp. GRB. Nucleic Acids Res. 1994 Apr 25;22(8):1476–1483. doi: 10.1093/nar/22.8.1476. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Zuerner R. L., Herrmann J. L., Saint Girons I. Comparison of genetic maps for two Leptospira interrogans serovars provides evidence for two chromosomes and intraspecies heterogeneity. J Bacteriol. 1993 Sep;175(17):5445–5451. doi: 10.1128/jb.175.17.5445-5451.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
