Abstract
DNA in the macronuclei of Oxytricha fallax, as in other hypotrichous ciliate protozoa, exists as small, achromosomal molecules rather than in chromosomes. We report studies on O. fallax DNA using physicochemical procedures and nucleic acid hybridization. Macronuclear DNA molecules range in size from 22 kilobase pairs (kb) to about 0.5 kb. The DNA has a buoyant density in CsCl of 1.694 g·cm-3 and a melting temperature in 15 mM NaCl/1.5 mM sodium citrate, pH 7, at 65.4°. These values correspond to 34.7% Gua + Cyt and 28.1% Gua + Cyt, respectively, and base composition determined by thin-layer chromatography of nucleotides is 32.4% Gua + Cyt. The only modified nucleotide that is detectable is N6-methyldeoxyadenylate (0.2%), and the amount and kind of modification cannot account for the discrepancies in nucleotide composition determination by the three methods. The genes for 25S and 19S rRNA are contained in DNA molecules 6.67 kb in length, of which at least 6.15 kb is transcribed. These rDNA molecules show no intrastrand complementarity as does rDNA in some other lower eukaryotes, and they have two asymmetric sites recognized by endonuclease EcoRI. The genes for 5S RNA are in DNA molecules 0.69 kb in length. Digestion of this DNA with restriction enzymes BamHI, BsuI, HhaI, and TaqI gives no evidence for a tandemly repeated sequence. It is likely that both 19S + 25S rRNA genes and 5S RNA genes in the Oxytricha macronucleus exist as single transcription units, and both may have “spacer” regions approximately 0.5 kb long.
Keywords: physicochemical properties of DNA, modified nucleotides, “gene-sized” DNA pieces, ribosomal DNA, 5S RNA genes
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- Ammermann D. Morphology and development of the macronuclei of the ciliates Stylonychia mytilus and Euplotes aediculatus. Chromosoma. 1971;33(2):209–238. doi: 10.1007/BF00285634. [DOI] [PubMed] [Google Scholar]
- Ammermann D., Steinbrück G., von Berger L., Hennig W. The development of the macronucleus in the ciliated protozoan Stylonychia mytilus. Chromosoma. 1974 May 10;45(4):401–429. doi: 10.1007/BF00283386. [DOI] [PubMed] [Google Scholar]
- Bostock C. J., Prescott D. M. Evidence of gene diminution during the formation of the macronucleus in the protozoan, Stylonychia (DNA density-melting curves-micronuclear DNA-polytene chromosomes). Proc Natl Acad Sci U S A. 1972 Jan;69(1):139–142. doi: 10.1073/pnas.69.1.139. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Botchan M., Topp W., Sambrook J. The arrangement of simian virus 40 sequences in the DNA of transformed cells. Cell. 1976 Oct;9(2):269–287. doi: 10.1016/0092-8674(76)90118-5. [DOI] [PubMed] [Google Scholar]
- Brown D. D., Dawid I. B. Specific gene amplification in oocytes. Oocyte nuclei contain extrachromosomal replicas of the genes for ribosomal RNA. Science. 1968 Apr 19;160(3825):272–280. doi: 10.1126/science.160.3825.272. [DOI] [PubMed] [Google Scholar]
- Carroll D., Brown D. D. Repeating units of Xenopus laevis oocyte-type 5S DNA are heterogeneous in length. Cell. 1976 Apr;7(4):467–475. doi: 10.1016/0092-8674(76)90198-7. [DOI] [PubMed] [Google Scholar]
- Cockburn A. F., Newkirk M. J., Firtel R. A. Organization of the ribosomal RNA genes of Dictyostelium discoideum: mapping of the nontranscribed spacer regions. Cell. 1976 Dec;9(4 Pt 1):605–613. doi: 10.1016/0092-8674(76)90043-x. [DOI] [PubMed] [Google Scholar]
- Corneo G., Ginelli E., Soave C., Bernardi G. Isolation and characterization of mouse and guinea pig satellite deoxyribonucleic acids. Biochemistry. 1968 Dec;7(12):4373–4379. doi: 10.1021/bi00852a033. [DOI] [PubMed] [Google Scholar]
- Denhardt D. T. A membrane-filter technique for the detection of complementary DNA. Biochem Biophys Res Commun. 1966 Jun 13;23(5):641–646. doi: 10.1016/0006-291x(66)90447-5. [DOI] [PubMed] [Google Scholar]
- Eckert W. A., Franke W. W., Scheer U. Nucleocytoplasmic translocation of RNA in Tetrahymena pyriformis and its inhibition by actinomycin D and cycloheximide. Exp Cell Res. 1975 Aug;94(1):31–46. doi: 10.1016/0014-4827(75)90528-5. [DOI] [PubMed] [Google Scholar]
- Erdmann V. A. Structure and function of 5S and 5.8 S RNA. Prog Nucleic Acid Res Mol Biol. 1976;18:45–90. [PubMed] [Google Scholar]
- Findly R. C., Gall J. G. Free ribosomal RNA genes in Paramecium are tandemly repeated. Proc Natl Acad Sci U S A. 1978 Jul;75(7):3312–3316. doi: 10.1073/pnas.75.7.3312. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Fink K., Adams W. S. Paper chromatographic data for purines, pyrimidines and derivatives in a variety of solvents. J Chromatogr. 1966 Apr;22(1):118–129. doi: 10.1016/s0021-9673(01)97077-3. [DOI] [PubMed] [Google Scholar]
- Firtel R. A., Lodish H. F. A small nuclear precursor of messenger RNA in the cellular slime mold Dictyostelium discoideum. J Mol Biol. 1973 Sep 15;79(2):295–314. doi: 10.1016/0022-2836(73)90007-7. [DOI] [PubMed] [Google Scholar]
- Gall J. G., Atherton D. D. Satellite DNA sequences in Drosophila virilis. J Mol Biol. 1974 Jan 5;85(4):633–664. doi: 10.1016/0022-2836(74)90321-0. [DOI] [PubMed] [Google Scholar]
- Gall J. G. Differential synthesis of the genes for ribosomal RNA during amphibian oögenesis. Proc Natl Acad Sci U S A. 1968 Jun;60(2):553–560. doi: 10.1073/pnas.60.2.553. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Gall J. G. Free ribosomal RNA genes in the macronucleus of Tetrahymena. Proc Natl Acad Sci U S A. 1974 Aug;71(8):3078–3081. doi: 10.1073/pnas.71.8.3078. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Gall J. G., Macgregor H. C., Kidston M. E. Gene amplification in the oocytes of Dytiscid water beetles. Chromosoma. 1969;26(2):169–187. doi: 10.1007/BF00326453. [DOI] [PubMed] [Google Scholar]
- Hershey N. D., Conrad S. E., Sodja A., Yen P. H., Cohen M., Jr, Davidson N., Iigen C., Carbon J. The sequence arrangement of Drosophila melanogaster 5s DNA cloned in recombinant plasmids. Cell. 1977 Jul;11(3):585–598. doi: 10.1016/0092-8674(77)90076-9. [DOI] [PubMed] [Google Scholar]
- Holmes D. S., Bonner J. Sequence composition of rat nuclear deoxyribonucleic acid and high molecular weight nuclear ribonucleic acid. Biochemistry. 1974 Feb 26;13(5):841–848. doi: 10.1021/bi00702a001. [DOI] [PubMed] [Google Scholar]
- 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]
- Kavenoff R., Zimm B. H. Chromosome-sized DNA molecules from Drosophila. Chromosoma. 1973;41(1):1–27. doi: 10.1007/BF00284071. [DOI] [PubMed] [Google Scholar]
- Kimmel A. R., Gorovsky M. A. Organization of the 5S RNA genes in macro- and micronuclei of Tetrahymena pyriformis. Chromosoma. 1978 Jun 23;67(1):1–20. doi: 10.1007/BF00285644. [DOI] [PubMed] [Google Scholar]
- Lauth M. R., Spear B. B., Heumann J., Prescott D. M. DNA of ciliated protozoa: DNA sequence diminution during macronuclear development of Oxytricha. Cell. 1976 Jan;7(1):67–74. doi: 10.1016/0092-8674(76)90256-7. [DOI] [PubMed] [Google Scholar]
- Lawn R. M., Heumann J. M., Herrick G., Prescott D. M. The gene-size DNA molecules in Oxytricha. Cold Spring Harb Symp Quant Biol. 1978;42(Pt 1):483–492. doi: 10.1101/sqb.1978.042.01.051. [DOI] [PubMed] [Google Scholar]
- Lima-De-Faria A., Birnstiel M., Jaworska H. Amplication of ribosomal cistrons in the heterochromatin of acheta. Genetics. 1969;61(1 Suppl):145–159. [PubMed] [Google Scholar]
- MARMUR J., DOTY P. Determination of the base composition of deoxyribonucleic acid from its thermal denaturation temperature. J Mol Biol. 1962 Jul;5:109–118. doi: 10.1016/s0022-2836(62)80066-7. [DOI] [PubMed] [Google Scholar]
- 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]
- 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]
- Prensky W., Steffensen D. M., Hughes W. L. The use of iodinated RNA for gene localization. Proc Natl Acad Sci U S A. 1973 Jun;70(6):1860–1864. doi: 10.1073/pnas.70.6.1860. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Prescott D. M., Murti K. G. Chromosome structure in ciliated protozoans. Cold Spring Harb Symp Quant Biol. 1974;38:609–618. doi: 10.1101/sqb.1974.038.01.065. [DOI] [PubMed] [Google Scholar]
- Rae P. M. 5-Hydroxymethyluracil in the DNA of a dinoflagellate. Proc Natl Acad Sci U S A. 1973 Apr;70(4):1141–1145. doi: 10.1073/pnas.70.4.1141. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Rae P. M. Hydroxymethyluracil in eukaryote DNA: a natural feature of the pyrrophyta (dinoflagellates). Science. 1976 Dec 3;194(4269):1062–1064. doi: 10.1126/science.988637. [DOI] [PubMed] [Google Scholar]
- Rae P. M., Steele R. E. Modified bases in the DNAs of unicellular eukaryotes: an examination of distributions and possible roles, with emphasis on hydroxymethyluracil in dinoflagellates. Biosystems. 1978 Apr;10(1-2):37–53. doi: 10.1016/0303-2647(78)90027-8. [DOI] [PubMed] [Google Scholar]
- Rigby P. W., Dieckmann M., Rhodes C., Berg P. Labeling deoxyribonucleic acid to high specific activity in vitro by nick translation with DNA polymerase I. J Mol Biol. 1977 Jun 15;113(1):237–251. doi: 10.1016/0022-2836(77)90052-3. [DOI] [PubMed] [Google Scholar]
- SCHILDKRAUT C. L., MARMUR J., DOTY P. Determination of the base composition of deoxyribonucleic acid from its buoyant density in CsCl. J Mol Biol. 1962 Jun;4:430–443. doi: 10.1016/s0022-2836(62)80100-4. [DOI] [PubMed] [Google Scholar]
- Scheller R. H., Thomas T. L., Lee A. S., Klein W. H., Niles W. D., Britten R. J., Davidson E. H. Clones of individual repetitive sequences from sea urchin DNA constructed with synthetic Eco RI sites. Science. 1977 Apr 8;196(4286):197–200. doi: 10.1126/science.847467. [DOI] [PubMed] [Google Scholar]
- 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]
- Spear B. B., Lauth M. R. Polytene chromosomes of Oxytricha: biochemical and morphological changes during macronuclear development in a ciliated protozoan. Chromosoma. 1976 Jan 27;54(1):1–13. doi: 10.1007/BF00331828. [DOI] [PubMed] [Google Scholar]
- 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]
- Wesley R. D. Inverted repetitious sequences in the macronuclear DNA of hypotrichous ciliates. Proc Natl Acad Sci U S A. 1975 Feb;72(2):678–682. doi: 10.1073/pnas.72.2.678. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Yao M. C., Kimmel A. R., Gorovsky M. A. A small number of cistrons for ribosomal RNA in the germinal nucleus of a eukaryote, Tetrahymena pyriformis. Proc Natl Acad Sci U S A. 1974 Aug;71(8):3082–3086. doi: 10.1073/pnas.71.8.3082. [DOI] [PMC free article] [PubMed] [Google Scholar]



