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. 1979 Apr;6(4):1433–1447. doi: 10.1093/nar/6.4.1433

Unique sequence arrangement of ribosomal genes in the palindromic rDNA molecule of Physarum polycephalum.

G R Campbell, V C Littau, P W Melera, V G Allfrey, E M Johnson
PMCID: PMC327781  PMID: 450702

Abstract

R-loop and restriction mapping procedures reveal the organization of coding regions at each end of the giant rDNA palindrome of Physarum polycephalum. A 19S coding region of 2.10 +/- 0.21 kb is located at each end of a very long central spacer (35.64 +/- 2.08 kb). An internal spacer of 1.66 +/- 0.12 kb lies distal to the 19S gene. The 5.8S rRNA coding region is located in this spacer. The 26S gene lies distal to the internal spacer. The 26S gene is unusual among those of eukaryotes in that it consists of 3 coding regions (alpha, beta and gamma) interrupted by 2 intervening sequences. The 26S alpha (most central) coding segment of 2.41 +/- 0.33 kb is separated from the 26S beta segment by an intervening sequence of 0.68 +/- 0.13 kb. The 26S beta segment (0.70 +/- 0.11 kb) is separated from the most distal 26S gamma segment (0.59 +/- 0.14 kb) by an intervening sequence of 1.21 +/- 0.14 kb. The 2 intervening sequences are present in at least 88% of ribsomal genes from active plasmodia, indicating that genes containing these sequences are transcribed. The rDNA termini contain a heterogeneous region which varies in length by +/- 300 base pairs.

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Selected References

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  1. Blackburn E. H., Gall J. G. A tandemly repeated sequence at the termini of the extrachromosomal ribosomal RNA genes in Tetrahymena. J Mol Biol. 1978 Mar 25;120(1):33–53. doi: 10.1016/0022-2836(78)90294-2. [DOI] [PubMed] [Google Scholar]
  2. Bohnert H. J., Schiller B. Circular DNA and rolling circles in nucleolar rDNA from mitotic nuclei of Physarum polycephalum. Eur J Biochem. 1975 Sep 15;57(2):361–369. doi: 10.1111/j.1432-1033.1975.tb02309.x. [DOI] [PubMed] [Google Scholar]
  3. Braun R., Evans T. E. Replication of nuclear satellite and mitochondrial DNA in the mitotic cycle of Physarum. Biochim Biophys Acta. 1969 Jun 17;182(2):511–522. doi: 10.1016/0005-2787(69)90203-2. [DOI] [PubMed] [Google Scholar]
  4. Cory S., Adams J. M. A very large repeating unit of mouse DNA containing the 18S, 28S and 5.8S rRNA genes. Cell. 1977 Aug;11(4):795–805. doi: 10.1016/0092-8674(77)90292-6. [DOI] [PubMed] [Google Scholar]
  5. Engberg J., Andersson P., Leick V., Collins J. Free ribosomal DNA molecules from Tetrahymena pyriformis GL are giant palindromes. J Mol Biol. 1976 Jun 25;104(2):455–470. doi: 10.1016/0022-2836(76)90281-3. [DOI] [PubMed] [Google Scholar]
  6. Frankel G., Cockburn A. F., Kindle K. L., Firtel R. A. Organization of the ribosomal RNA genes of Dictyostelium discoideum. Mapping of the transcribed region. J Mol Biol. 1977 Feb 5;109(4):539–558. doi: 10.1016/s0022-2836(77)80090-9. [DOI] [PubMed] [Google Scholar]
  7. Gross-Bellard M., Oudet P., Chambon P. Isolation of high-molecular-weight DNA from mammalian cells. Eur J Biochem. 1973 Jul 2;36(1):32–38. doi: 10.1111/j.1432-1033.1973.tb02881.x. [DOI] [PubMed] [Google Scholar]
  8. Hall L., Braun R. The organisation of genes for transfer RNA and ribosomal RNA in amoebae and plasmodia of Physarum polycephalum. Eur J Biochem. 1977 Jun 1;76(1):165–174. doi: 10.1111/j.1432-1033.1977.tb11582.x. [DOI] [PubMed] [Google Scholar]
  9. Jacobson D. N., Holt C. E. Isolation of ribosomal RNA precursors from Physarum polycephalum. Arch Biochem Biophys. 1973 Nov;159(1):342–352. doi: 10.1016/0003-9861(73)90460-8. [DOI] [PubMed] [Google Scholar]
  10. Karrer K. M., Gall J. G. The macronuclear ribosomal DNA of Tetrahymena pyriformis is a palindrome. J Mol Biol. 1976 Jun 25;104(2):421–453. doi: 10.1016/0022-2836(76)90280-1. [DOI] [PubMed] [Google Scholar]
  11. Leon W., Fouts D. L., Manning J. Sequence arrangement of the 16S and 26S rRNA genes in the pathogenic haemoflagellate Leishmania donovani. Nucleic Acids Res. 1978 Feb;5(2):491–504. doi: 10.1093/nar/5.2.491. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Maizels N. Dictyostelium 17S, 25S, and 5S rDNAs lie within a 38,000 base pair repeated unit. Cell. 1976 Nov;9(3):431–438. doi: 10.1016/0092-8674(76)90088-x. [DOI] [PubMed] [Google Scholar]
  13. Melera P. W., Rusch H. P. A characterization of ribonucleic acid in the myxomycete Physarum polycephalum. Exp Cell Res. 1973 Nov;82(1):197–209. doi: 10.1016/0014-4827(73)90262-0. [DOI] [PubMed] [Google Scholar]
  14. Mohberg J., Rusch H. P. Isolation and DNA content of nuclei of Physarum polycephalum. Exp Cell Res. 1971 Jun;66(2):305–316. doi: 10.1016/0014-4827(71)90682-3. [DOI] [PubMed] [Google Scholar]
  15. Molgaard H. V., Matthews H. R., Bradbury E. M. Organisation of genes for ribosomal RNA in Physarum polycephalum. Eur J Biochem. 1976 Sep 15;68(2):541–549. doi: 10.1111/j.1432-1033.1976.tb10842.x. [DOI] [PubMed] [Google Scholar]
  16. Murray K., Murray N. E. Phage lambda receptor chromosomes for DNA fragments made with restriction endonuclease III of Haemophilus influenzae and restriction endonuclease I of Escherichia coli. J Mol Biol. 1975 Nov 5;98(3):551–564. doi: 10.1016/s0022-2836(75)80086-6. [DOI] [PubMed] [Google Scholar]
  17. Newlon C. S., Sonenshein G. E., Holt C. E. Time of synthesis for ribosomal ribonucleic acid in Physarum. Biochemistry. 1973 Jun 5;12(12):2338–2345. doi: 10.1021/bi00736a024. [DOI] [PubMed] [Google Scholar]
  18. Pellegrini M., Manning J., Davidson N. Sequence arrangement of the rDNA of Drosophila melanogaster. Cell. 1977 Feb;10(2):213–214. doi: 10.1016/0092-8674(77)90215-x. [DOI] [PubMed] [Google Scholar]
  19. Philippsen P., Thomas M., Kramer R. A., Davis R. W. Unique arrangement of coding sequences for 5 S, 5.8 S, 18 S and 25 S ribosomal RNA in Saccharomyces cerevisiae as determined by R-loop and hybridization analysis. J Mol Biol. 1978 Aug 15;123(3):387–404. doi: 10.1016/0022-2836(78)90086-4. [DOI] [PubMed] [Google Scholar]
  20. Ryser U., Braun R. The amount of DNA coding for rRNA during differentiation (spherulation) in Physarum polycephalum. Biochim Biophys Acta. 1974 Aug 15;361(1):33–36. doi: 10.1016/0005-2787(74)90206-8. [DOI] [PubMed] [Google Scholar]
  21. Sanger F., Coulson A. R., Friedmann T., Air G. M., Barrell B. G., Brown N. L., Fiddes J. C., Hutchison C. A., 3rd, Slocombe P. M., Smith M. The nucleotide sequence of bacteriophage phiX174. J Mol Biol. 1978 Oct 25;125(2):225–246. doi: 10.1016/0022-2836(78)90346-7. [DOI] [PubMed] [Google Scholar]
  22. Southern E. M. Detection of specific sequences among DNA fragments separated by gel electrophoresis. J Mol Biol. 1975 Nov 5;98(3):503–517. doi: 10.1016/s0022-2836(75)80083-0. [DOI] [PubMed] [Google Scholar]
  23. Speirs J., Birnstiel M. Arrangement of the 5-8 S RNA cistrons in the genome of Xenopus laevis. J Mol Biol. 1974 Aug 5;87(2):237–256. doi: 10.1016/0022-2836(74)90146-6. [DOI] [PubMed] [Google Scholar]
  24. Thomas M., White R. L., Davis R. W. Hybridization of RNA to double-stranded DNA: formation of R-loops. Proc Natl Acad Sci U S A. 1976 Jul;73(7):2294–2298. doi: 10.1073/pnas.73.7.2294. [DOI] [PMC free article] [PubMed] [Google Scholar]
  25. Vogt V. M., Braun R. Structure of ribosomal DNA in Physarum polycephalum. J Mol Biol. 1976 Sep 25;106(3):567–587. doi: 10.1016/0022-2836(76)90252-7. [DOI] [PubMed] [Google Scholar]
  26. Wellauer P. K., Dawid I. B. The structural organization of ribosomal DNA in Drosophila melanogaster. Cell. 1977 Feb;10(2):193–212. doi: 10.1016/0092-8674(77)90214-8. [DOI] [PubMed] [Google Scholar]
  27. White R. L., Hogness D. S. R loop mapping of the 18S and 28S sequences in the long and short repeating units of Drosophila melanogaster rDNA. Cell. 1977 Feb;10(2):177–192. doi: 10.1016/0092-8674(77)90213-6. [DOI] [PubMed] [Google Scholar]

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