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PMID: 1901370 Published · ppublish English Comparative Study Journal Article Research Support, Non-U.S. Gov't

Evolution of RNA polymerases and branching patterns of the three major groups of Archaebacteria.

Journal of molecular evolution ·Vol. 32 ·No. 1 ·1991-01-00 ·Pages 70-8

Iwabe N, Kuma K, Kishino H, Hasegawa M, Miyata T

Abstract

The amino acid sequences of the largest subunits of the RNA polymerases I, II, and III from eukaryotes were compared with those of archaebacterial and eubacterial homologs, and their evolutionary relationships were analyzed in detail by a recently developed tree-making method, the likelihood method of protein phylogeny, as well as by the neighbor-joining method and the parsimony method, together with bootstrap analyses. It was shown that the best tree topologies predicted by the first two methods are identical, whereas the last one predicts a distinct tree. The maximum likelihood tree revealed that, after the separation from archaebacteria, the three eukaryotic RNA polymerases diverged from an ancestral precursor in the eukaryotic lineage. This result is contrasted with the published result showing multiple origins for the three eukaryotic polymerases. It was shown that eukaryotic RNA polymerase I evolved much more rapidly than RNA polymerases II and III: The N-terminal half of RNA polymerase I shows an extraordinarily high evolutionary rate, possibly due to relaxed functional constraints. In contrast the evolutionary rate of archaebacterial RNA polymerase is remarkably limited. In addition, including the second largest subunit of the RNA polymerase, a detailed analysis for the branching pattern of the three major groups of archaebacteria was carried out by the maximum likelihood method. It was shown that the three major groups of archaebacteria are likely to form a single cluster; that is, archaebacteria are likely to be monophyletic as originally proposed by Woese and his colleagues.

MeSH Terms
Amino Acid Sequence Animals Archaea/enzymology,genetics Biological Evolution DNA-Directed RNA Polymerases/genetics Mice Molecular Sequence Data Phylogeny Sequence Homology, Nucleic Acid
Chemicals
DNA-Directed RNA Polymerases
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Iwabe N
Department of Biology, Faculty of Science, Kyushu University, Fukuoka, Japan.
Kuma K
Kishino H
Hasegawa M
Miyata T
References (28)
28 references, click to expand
  1. Trypanosoma brucei contains two RNA polymerase II largest subunit genes with an altered C-terminal domain.
    Cell. 1989 Feb 24;56(4):585-97 PMID: 2917367
  2. Relatedness of archaebacterial RNA polymerase core subunits to their eubacterial and eukaryotic equivalents.
    Nucleic Acids Res. 1988 Aug 25;16(16):8113-28 PMID: 2843811
  3. Nucleotide sequence and expression of the cloned gene of bacteriophage SP6 RNA polymerase.
    Nucleic Acids Res. 1987 Mar 25;15(6):2653-64 PMID: 3031606
  4. The neighbor-joining method: a new method for reconstructing phylogenetic trees.
    Mol Biol Evol. 1987 Jul;4(4):406-25 PMID: 3447015
  5. The primary structure of E. coli RNA polymerase, Nucleotide sequence of the rpoC gene and amino acid sequence of the beta'-subunit.
    Nucleic Acids Res. 1982 Jul 10;10(13):4035-44 PMID: 6287430
  6. Structure and sequence of the gene for the largest subunit of trypanosomal RNA polymerase III.
    Nucleic Acids Res. 1988 Sep 26;16(18):8753-72 PMID: 3174432
  7. Structure of the eukaryotic transcription apparatus: features of the gene for the largest subunit of Drosophila RNA polymerase II.
    Cell. 1985 Sep;42(2):611-21 PMID: 2992806
  8. CONFIDENCE LIMITS ON PHYLOGENIES: AN APPROACH USING THE BOOTSTRAP.
    Evolution. 1985 Jul;39(4):783-791 PMID: 28561359
  9. Phylogenetic structure of the prokaryotic domain: the primary kingdoms.
    Proc Natl Acad Sci U S A. 1977 Nov;74(11):5088-90 PMID: 270744
  10. Origin of the eukaryotic nucleus determined by rate-invariant analysis of rRNA sequences.
    Nature. 1988 Jan 14;331(6152):184-6 PMID: 3340165
  11. Homology between RNA polymerases of poxviruses, prokaryotes, and eukaryotes: nucleotide sequence and transcriptional analysis of vaccinia virus genes encoding 147-kDa and 22-kDa subunits.
    Proc Natl Acad Sci U S A. 1986 May;83(10 ):3141-5 PMID: 3517852
  12. Eocytes: a new ribosome structure indicates a kingdom with a close relationship to eukaryotes.
    Proc Natl Acad Sci U S A. 1984 Jun;81(12):3786-90 PMID: 6587394
  13. Bacterial evolution.
    Microbiol Rev. 1987 Jun;51(2):221-71 PMID: 2439888
  14. The primary structure of Escherichia coli RNA polymerase. Nucleotide sequence of the rpoB gene and amino-acid sequence of the beta-subunit.
    Eur J Biochem. 1981 Jun 1;116(3):621-9 PMID: 6266829
  15. Cloning and sequence analysis of the mouse genomic locus encoding the largest subunit of RNA polymerase II.
    J Biol Chem. 1987 Aug 5;262(22):10695-705 PMID: 3038894
  16. Evolutionary relationship of archaebacteria, eubacteria, and eukaryotes inferred from phylogenetic trees of duplicated genes.
    Proc Natl Acad Sci U S A. 1989 Dec;86(23):9355-9 PMID: 2531898
  17. RNA polymerase II of Drosophila. Relation of its 140,000 Mr subunit to the beta subunit of Escherichia coli RNA polymerase.
    J Mol Biol. 1987 Jun 20;195(4):929-37 PMID: 3116266
  18. Prokaryotic and eukaryotic RNA polymerases have homologous core subunits.
    Proc Natl Acad Sci U S A. 1987 Mar;84(5):1192-6 PMID: 3547406
  19. The complete nucleotide sequence of the tobacco chloroplast genome: its gene organization and expression.
    EMBO J. 1986 Sep;5(9):2043-2049 PMID: 16453699
  20. Archaebacterial DNA-dependent RNA polymerases testify to the evolution of the eukaryotic nuclear genome.
    Proc Natl Acad Sci U S A. 1989 Jun;86(12):4569-73 PMID: 2499884
  21. Sequence, organization, transcription and evolution of RNA polymerase subunit genes from the archaebacterial extreme halophiles Halobacterium halobium and Halococcus morrhuae.
    J Mol Biol. 1989 Mar 5;206(1):1-17 PMID: 2495365
  22. Cloning and sequence determination of the gene encoding the largest subunit of the fission yeast Schizosaccharomyces pombe RNA polymerase I.
    Gene. 1988 Dec 30;74(2):503-15 PMID: 2854522
  23. Nucleotide sequence of the gene for bacteriophage T7 RNA polymerase.
    J Mol Biol. 1984 Feb 25;173(2):265-9 PMID: 6708104
  24. Extensive homology among the largest subunits of eukaryotic and prokaryotic RNA polymerases.
    Cell. 1985 Sep;42(2):599-610 PMID: 3896517
  25. Sequence and analysis of the gene for bacteriophage T3 RNA polymerase.
    Nucleic Acids Res. 1985 Sep 25;13(18):6753-66 PMID: 3903658
  26. Yeast mitochondrial RNA polymerase is homologous to those encoded by bacteriophages T3 and T7.
    Cell. 1987 Oct 9;51(1):89-99 PMID: 3308116
  27. RPA190, the gene coding for the largest subunit of yeast RNA polymerase A.
    J Biol Chem. 1988 Feb 25;263(6):2830-9 PMID: 2830265
  28. Evaluation of the maximum likelihood estimate of the evolutionary tree topologies from DNA sequence data, and the branching order in hominoidea.
    J Mol Evol. 1989 Aug;29(2):170-9 PMID: 2509717
Article Info
Journal
Journal of molecular evolution
Abbr.
J Mol Evol
ISSN
0022-2844
Published
1991-01-00
Pages
70-8
Language
English
Region
Germany
NLM ID
0360051
Subset
IM
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