Skip to main content
PMC home page
Proceedings of the National Academy of Sciences of the United States of America logoLink to Proceedings of the National Academy of Sciences of the United States of America
. 1996 Aug 20;93(17):8797–8799. doi: 10.1073/pnas.93.17.8797

At the core of the Archaea.

W F Doolittle 1
PMCID: PMC38545  PMID: 8799104

Full text

PDF
8797

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Baldauf S. L., Palmer J. D., Doolittle W. F. The root of the universal tree and the origin of eukaryotes based on elongation factor phylogeny. Proc Natl Acad Sci U S A. 1996 Jul 23;93(15):7749–7754. doi: 10.1073/pnas.93.15.7749. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Barns S. M., Delwiche C. F., Palmer J. D., Pace N. R. Perspectives on archaeal diversity, thermophily and monophyly from environmental rRNA sequences. Proc Natl Acad Sci U S A. 1996 Aug 20;93(17):9188–9193. doi: 10.1073/pnas.93.17.9188. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Barns S. M., Fundyga R. E., Jeffries M. W., Pace N. R. Remarkable archaeal diversity detected in a Yellowstone National Park hot spring environment. Proc Natl Acad Sci U S A. 1994 Mar 1;91(5):1609–1613. doi: 10.1073/pnas.91.5.1609. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Brown J. R., Masuchi Y., Robb F. T., Doolittle W. F. Evolutionary relationships of bacterial and archaeal glutamine synthetase genes. J Mol Evol. 1994 Jun;38(6):566–576. doi: 10.1007/BF00175876. [DOI] [PubMed] [Google Scholar]
  5. Clark C. G., Roger A. J. Direct evidence for secondary loss of mitochondria in Entamoeba histolytica. Proc Natl Acad Sci U S A. 1995 Jul 3;92(14):6518–6521. doi: 10.1073/pnas.92.14.6518. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. DeLong E. F. Archaea in coastal marine environments. Proc Natl Acad Sci U S A. 1992 Jun 15;89(12):5685–5689. doi: 10.1073/pnas.89.12.5685. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Golding G. B., Gupta R. S. Protein-based phylogenies support a chimeric origin for the eukaryotic genome. Mol Biol Evol. 1995 Jan;12(1):1–6. doi: 10.1093/oxfordjournals.molbev.a040178. [DOI] [PubMed] [Google Scholar]
  8. Huber R., Burggraf S., Mayer T., Barns S. M., Rossnagel P., Stetter K. O. Isolation of a hyperthermophilic archaeum predicted by in situ RNA analysis. Nature. 1995 Jul 6;376(6535):57–58. doi: 10.1038/376057a0. [DOI] [PubMed] [Google Scholar]
  9. Keeling P. J., Doolittle W. F. Archaea: narrowing the gap between prokaryotes and eukaryotes. Proc Natl Acad Sci U S A. 1995 Jun 20;92(13):5761–5764. doi: 10.1073/pnas.92.13.5761. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Lake J. A. Origin of the eukaryotic nucleus determined by rate-invariant analysis of rRNA sequences. Nature. 1988 Jan 14;331(6152):184–186. doi: 10.1038/331184a0. [DOI] [PubMed] [Google Scholar]
  11. Margolin W., Wang R., Kumar M. Isolation of an ftsZ homolog from the archaebacterium Halobacterium salinarium: implications for the evolution of FtsZ and tubulin. J Bacteriol. 1996 Mar;178(5):1320–1327. doi: 10.1128/jb.178.5.1320-1327.1996. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Mayr E. Biological classification: toward a synthesis of opposing methodologies. Science. 1981 Oct 30;214(4520):510–516. doi: 10.1126/science.214.4520.510. [DOI] [PubMed] [Google Scholar]
  13. Potter S., Durovic P., Dennis P. P. Ribosomal RNA precursor processing by a eukaryotic U3 small nucleolar RNA-like molecule in an archaeon. Science. 1995 May 19;268(5213):1056–1060. doi: 10.1126/science.7538698. [DOI] [PubMed] [Google Scholar]
  14. Schwartz R. M., Dayhoff M. O. Origins of prokaryotes, eukaryotes, mitochondria, and chloroplasts. Science. 1978 Jan 27;199(4327):395–403. doi: 10.1126/science.202030. [DOI] [PubMed] [Google Scholar]
  15. Smith M. W., Feng D. F., Doolittle R. F. Evolution by acquisition: the case for horizontal gene transfers. Trends Biochem Sci. 1992 Dec;17(12):489–493. doi: 10.1016/0968-0004(92)90335-7. [DOI] [PubMed] [Google Scholar]
  16. Starich M. R., Sandman K., Reeve J. N., Summers M. F. NMR structure of HMfB from the hyperthermophile, Methanothermus fervidus, confirms that this archaeal protein is a histone. J Mol Biol. 1996 Jan 12;255(1):187–203. doi: 10.1006/jmbi.1996.0016. [DOI] [PubMed] [Google Scholar]
  17. Stein J. L., Marsh T. L., Wu K. Y., Shizuya H., DeLong E. F. Characterization of uncultivated prokaryotes: isolation and analysis of a 40-kilobase-pair genome fragment from a planktonic marine archaeon. J Bacteriol. 1996 Feb;178(3):591–599. doi: 10.1128/jb.178.3.591-599.1996. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Woese C. R. Bacterial evolution. Microbiol Rev. 1987 Jun;51(2):221–271. doi: 10.1128/mr.51.2.221-271.1987. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Woese C. R., Kandler O., Wheelis M. L. Towards a natural system of organisms: proposal for the domains Archaea, Bacteria, and Eucarya. Proc Natl Acad Sci U S A. 1990 Jun;87(12):4576–4579. doi: 10.1073/pnas.87.12.4576. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. Zuckerkandl E., Pauling L. Molecules as documents of evolutionary history. J Theor Biol. 1965 Mar;8(2):357–366. doi: 10.1016/0022-5193(65)90083-4. [DOI] [PubMed] [Google Scholar]

Articles from Proceedings of the National Academy of Sciences of the United States of America are provided here courtesy of National Academy of Sciences

RESOURCES