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Molecular Reorganization During Nuclear Differentiation in Ciliates

  • Chapter
Germ Line — Soma Differentiation

Part of the book series: Results and Problems in Cell Differentiation ((RESULTS,volume 13))

Abstract

Differentiation denotes the process by which cells of multicellular organisms become different from one another. The closely related process by which nuclei become functionally and/or structurally different from one another can be called nuclear differentiation. Nuclear differentiation is a well-known, but often poorly understood phenomenon. For instance, large differences exist between gamete nuclei, e.g., sperm nuclei and somatic nuclei of the same organism, with regards to nuclear size, chromatin condensation, transcriptional activity, structure of the nuclear lamina, and many other characteristics. But differences in nuclear structure and in the organization of the genetic material also occur between different somatic nuclei. Differing amounts of eu-and heterochromatin, DNA rearrangements during cellular development, or amplification of certain genes may give rise to the existence of nuclei which differ from one another despite their common origin from one zygote nucleus.

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References

  • Allis CD, Glover CVC, Gorovsky MA (1979) Micronuclei of Tetrahymena contain two types of histone H3. Proc Natl Acad Sci USA 76: 4857–4861

    PubMed  CAS  Google Scholar 

  • Allis CD, Bowen JK, Abraham GN, Glover CVC, Gorovsky MA (1980 a) Proteolytic processing of histone H3 in chromatin: a physiologically regulated event in Tetrahymena micronuclei. Cell 20: 55–64

    Google Scholar 

  • Allis CD, Glover CVC, Bowen JK, Gorovsky MA ( 1980 b) Histone variants specific to the transcriptionally active, amitotically dividing macronucleus of the unicellular eucaryote, Tetrahymena thermophila. Cell 20: 609–617

    Google Scholar 

  • Allis CD, Ziegler YS, Gorovsky MA, Olmsted JB (1982) A conserved histone variant enriched in nucleoli of mammalian cells. Cell 31: 131–136

    PubMed  CAS  Google Scholar 

  • Allis CD, Wiggins JC, Richman R, Chicoine L, Wenkert D (1984) Histone rearrangements accompany nuclear differentiation and dedifferentiation in Tetrahymena thermophila. In: Abstracts of papers presented at the meeting on “Ciliate molecular genetics” 2.5.-6.5. 1984. Cold Spring Harbor Laboratory, New York

    Google Scholar 

  • Alonso P, Jareno MA (1974) Incorporacion de uridina-H3 en el esbozo macronuclear de Stylonychia mytilus. Microbiol Esp 27: 199–211

    PubMed  CAS  Google Scholar 

  • Alonso P, Pérez-Silva J (1965) Giant chromosomes in protozoa. Nature (Lond) 205:313–314 Amabis JM (1983) DNA-puffing patterns in the salivary glands of Trichosia pubescens ( Diptera, Sciaridae). Genetica (The Hague ) 62: 3–13

    Google Scholar 

  • Ammermann D (1965) Cytologische und genetische Untersuchungen an dem Ciliaten Stylonychia mytilus Ehrenberg. Arch Protistenkd 108: 109–152

    Google Scholar 

  • Ammermann D (1970) The micronucleus of the ciliate Stylonychia mytilus, its nucleic acid synthesis and its function. Exp Cell Res 61: 6–12

    PubMed  CAS  Google Scholar 

  • Ammermann D (1971) Morphology and development of the macronuclei of the ciliates Stylonychia mytilus and Euplotes aediculatus. Chromosoma (Berl) 33: 209–238

    CAS  Google Scholar 

  • Ammermann D (1982) Mating types in Stylonychia mytilus Ehrenberg. Arch Protistenkd 126: 373–381

    Google Scholar 

  • Ammermann D, Muenz A (1982) DNA and protein content of different hypotrich ciliates. Eur J Cell Biol 27: 22–24

    PubMed  CAS  Google Scholar 

  • Ammermann D, Schlegel M (1983) Characterization of two sibling species of the genus Stylonychia (Ciliata, Hypotricha): S. mytilus Ehrenberg, 1838 and S. lemnae n. sp. I. Morphology and reproductive behavior. J Protozool 30: 290–294

    Google Scholar 

  • Ammermann D, Steinbrück G, v Berger L, Hennig W (1974) The development of the macronu- cleus in the ciliated protozoan, Stylonychia mytilus. Chromosoma (Berl) 45: 401–429

    Google Scholar 

  • Ammermann D, Steinbrück G, Baur R, Wohlert H (1981) Methylated bases in the DNA of the ciliate, Stylonychia mytilus. Eur J Cell Biol 24: 154–156

    Google Scholar 

  • Ax P (1966) Die Bedeutung der interstitiellen Sandfauna für allgemeine Probleme der Systematik, Ökologie und Biologie. Veröff Inst Meeresforsch Bremerhaven, Suppl 2: 15–66

    Google Scholar 

  • Balbiani EG (1890) Etude sur le Loxode. Ann Micrograph 2: 401–431

    Google Scholar 

  • Bannon GA, Bowen JK, Yao M-C, Gorovsky MA (1984) Tetrahymena H4 genes: structure, evo-lution and organization in macro-and micronuclei. Nucleic Acids Res 12: 1961–1975

    PubMed  CAS  Google Scholar 

  • Berger JD (1973) Nuclear differentiation and nucleic acid synthesis in well-fed exconjugants of Paramecium aurelia. Chromosoma (Berl) 42: 247–268

    CAS  Google Scholar 

  • Blackburn EH (1982) Characterization and species differences of rDNA: protozoa. In: Busch H, Rothblum L (eds) The cell nucleus, vol 10. Academic Press, New York, p 145–170 Blackburn EH (1984) Telomers: Do the ends justify the means? Cell 37: 7–8

    Google Scholar 

  • Blackburn EH, Challoner PB (1984) Identification of a telomeric DNA sequence in Trypanosoma brucei. Cell 36: 447–457

    PubMed  CAS  Google Scholar 

  • Blackburn EH, Gall JG (1978) A tandemly repeated sequence at the termini of the extrachromosomal ribosomal RNA genes in Tetrahymena. J Mol Biol 120: 33–53

    PubMed  CAS  Google Scholar 

  • Blackburn EH, Szostak JW (1984) The molecular structure of centromeres and telomeres. Annu Rev Biochem 53: 163–194

    PubMed  CAS  Google Scholar 

  • Blackburn EH, Budarf ML, Challoner PB, Cherry JM, Howard EA, Katzen AL, Pan W-C, Ryan T (1983) DNA termini in ciliate macronuclei. Cold Spring Harborg Symp Quant Biol 47: 1195–1207

    Google Scholar 

  • Bobyleva NN, Kudrjavtsev BN, Raikov IB (1980) Changes of the DNA content of differentiating and adult macronuclei of the ciliate, Loxodes magnus ( Karyorelictida ). J Cell Sci 44: 375394

    Google Scholar 

  • Borchsenius SN, Sergejeva GI (1979) Characterization of DNA from the ciliate, Bursaria truncatella O. F. Müller, vegetative cells. Tsitologiya 21: 327–333 (in Russian with English summary)

    Google Scholar 

  • Borden D, Whitt GS, Nanney DL (1973) Electrophoretic characterization of classical Tetrahymena pyriformis strains. J Protozool 20: 693–700

    PubMed  CAS  Google Scholar 

  • Borden D, Miller ET, Whitt GS, Nanney DL (1977) Electrophoretic analysis of evolutionary relationships in Tetrahymena. Evolution 31: 91–102

    CAS  Google Scholar 

  • Borst P, Cross GAM (1982) Molecular basis for trypanosome antigenic variation. Cell 29: 291303

    Google Scholar 

  • Bostock CJ, Prescott DM (1972) Evidence of gene diminution during the formation of the macronucleus in the protozoan Stylonychia. Proc Natl Acad Sci USA 69: 139–142

    PubMed  CAS  Google Scholar 

  • Boswell RE, Klobutcher LA, Prescott DM (1982) Inverted terminal repeats are added to genes during macronuclear development in Oxytricha nova. Proc Natl Acad Sci USA 79: 32553259

    Google Scholar 

  • Boswell RE, Jahn CL, Greslin AF, Prescott DM (1983) Organization of gene and non-gene se-quences in micronuclear DNA of Oxytricha nova. Nucleic Acids Res 11: 3651–3663

    PubMed  CAS  Google Scholar 

  • Brachet J, Bonotto S (eds) (1970) Biology of Acetabularia. Elsevier/North-Holland, Amster-dam

    Google Scholar 

  • Brunk CF, Tsao SGS, Diamond CH, Ohshi PS, Tsao NNG, Pearlman RE (1982) Reorganization of unique and repetitive sequences during nuclear development in Tetrahymena thermophila. Can J Biochem 60: 847–853

    PubMed  CAS  Google Scholar 

  • Bruns PJ (1984) Tetrahymena thermophila. In: O’Brien SJ (ed) Genetic maps 1984. Cold Spring Harbor Laboratory, New York, pp 211–215

    Google Scholar 

  • Bruns PJ, Brussard TEB (1981) Nullisomic Tetrahymena: eliminating germinal chromosomes. Science (Wash DC) 213: 549–551

    CAS  Google Scholar 

  • Bütschli 0 (1876) Studien über die ersten Entwicklungsvorgänge der Eizelle, die Zellteilung and die Conjugation der Infusorien. Abhandl Senckenberg Naturforsch Ges 10: 213–464

    Google Scholar 

  • Callahan RC, Shalke G, Gorovsky MA (1984) Developmental rearrangements associated with a single type of expressed a-tubulin gene in Tetrahymena. Cell 36: 441–445

    PubMed  CAS  Google Scholar 

  • Calos MP, Miller JH (1980) Transposable elements. Cell 20: 579–595

    PubMed  CAS  Google Scholar 

  • Caplan EB (1975) A very rapidly migrating fl histone associated with gene-sized pieces of DNA in the macronucleus of Oxytricha sp. Biochim Biophys Acta 407: 109–113

    PubMed  CAS  Google Scholar 

  • Caplan EB (1977) Histones and other basic nuclear proteins in genetically active and genetically inactive nuclei of the ciliate, Oxytricha sp. Biochim Biophys Acta 479: 214–219

    PubMed  CAS  Google Scholar 

  • Cartinhour SW, Herrick GA (1984 a) Three different macronuclear DNAs in Oxytricha fallax share a common sequence block. Mol Cell Biol 4: 931–938

    Google Scholar 

  • Cartinhour S, Herrick G (1984b) Alternate juxtaposition of macronuclear sequences in Oxytricha fallax. In: Abstracts of papers presented at the meeting on “Ciliate molecular genetics” 2.5.-6.5. 1984. Cold Spring Harbor Laboratory, New York, p 6

    Google Scholar 

  • Cavalier-Smith T (1978) Nuclear volume control by nucleoskeletal DNA, selection for cell volume and cell growth rate, and the solution of the C-value paradox. J Cell Sci 34:247–278 Cavalier-Smith T (1980) How selfish is DNA? Nature (Lond) 285: 617–618

    Google Scholar 

  • Cavalier-Smith T (1982) Skeletal DNA and the evolution of genome size. Annu Rev Biophys Bioeng 11: 273–302

    PubMed  CAS  Google Scholar 

  • Chen TT (1940) Polyploidy in Paramecium bursaria. Proc Natl Acad Sci USA 26:239–340 Cleffmann G (1968) Regulierung der DNS-Menge im Makronucleus von Tetrahymena. Exp Cell Res 50: 193–207

    Google Scholar 

  • Conner RL, Koroly MJ (1973) Chemistry and metabolism of nucleic acids in Tetrahymena. In: Elliott AM (ed) Biology of Tetrahymena. Dowden, Hutchinson and Ross, Stroudsburg, Pa Corliss JO ( 1979 ) The ciliated protozoa. Pergamon, Oxford

    Google Scholar 

  • Corliss JO, Hartwig E (1977) The „primitive“ interstitial ciliates: Their ecology, nuclear uniqueness, and postulated place in the evolution and systematics of the phylum Ciliophora. Mikrofauna Meeresboden 61: 65–88

    Google Scholar 

  • Cullis CA (1972) The basis of cell-to-cell transformation in Paramecium bursaria. II. Investiga- tion into the molecular nature of the transforming agent. J Cell Sci 11: 611–619

    PubMed  CAS  Google Scholar 

  • Cullis CA (1973) DNA amounts in the nuclei of Paramecium bursaria. Chromosoma (Berl) 40: 127–133

    CAS  Google Scholar 

  • Cummings DJ (1975) Studies on macronuclear DNA from Paramecium aurelia. Chromosoma (Berl) 53: 191–208

    CAS  Google Scholar 

  • Cummings DJ, Tait A (1975) The isolation of nuclei from Paramecium aurelia. In: Prescott DM (ed) Methods in cell biology, vol 9. Academic Press, New York, pp 281–309

    Google Scholar 

  • Czihak G (1964) Experiments on nuclear differentiation in the foraminifer Rotaliella heterokaryotica Grell by means of UV-irradiation. Exp Cell Res 35: 372–380

    PubMed  CAS  Google Scholar 

  • Dani GM, Zakian VA (1983) Mitotic and meiotic stability of linear plasmids in yeast. Proc Natl Acad Sci USA 80: 3406–3410

    PubMed  CAS  Google Scholar 

  • Dawson D, Herrick G (1982) Micronuclear DNA sequences of Oxytricha fallax homologous to the macronuclear inverted terminal repeat. Nucleic Acids Res 10: 2911–2924

    PubMed  CAS  Google Scholar 

  • Dawson D, Herrick G (1984) Telomeric properties of C4A4-homologous sequences in micronuclear DNA of Oxytricha fallax. Cell 36: 171–177

    PubMed  CAS  Google Scholar 

  • Diamond CH, Ohashi PS, Rose A, Tsao NNG, Pearlman E (1984) Analysis of a micronucleus limited sequence from Tetrahymena thermophila. In: Abstracts of papers presented at the meeting on „Ciliate molecular genetics“ 2.5.-6.5. 1984. Cold Spring Harbor Laboratory, New York, p 10

    Google Scholar 

  • Dittmann F-N (1978) Untersuchungen zur Wirkung von UV- und Röntgenstrahlen und zur Re-paratur der Strahlenschäden bei dem Ciliaten Stylonychia mytilus. Thesis Univ Tübingen

    Google Scholar 

  • Doerder FP (1979) Regulation of macronuclear DNA content in Tetrahymena thermophila. J Protozool 26: 28–35

    CAS  Google Scholar 

  • Doerder FP, DeBault LE (1975) Cytofluorometric analysis of nuclear DNA during meiosis, fertilization and macronuclear development in the ciliate, Tetrahymena pyriformis. J Cell Sci 17: 47–93

    Google Scholar 

  • Doolittle WF, Sapienza C (1980) Selfish genes, the phenotype paradigm and genome evolution. Nature (Lond) 284: 601–603

    CAS  Google Scholar 

  • Dover G (1980) Ignorant DNA. Nature (Lond) 285: 618–620

    CAS  Google Scholar 

  • Dover G, Doolittle WF (1980) Modes of genome evolution. Nature (Lond) 288:646–647 Dragesco J (1960) Ciliés mésopsammique littoraux. Systematique morphologie, écologie. Tray Stat Biol Roscoff (NS) 12: 1–356

    Google Scholar 

  • Elsevier SM, Lipps HJ, Steinbrück G (1978) Histone genes in macronuclear DNA of the ciliate Stylonychia mytilus. Chromosoma (Berl) 69: 291–306

    CAS  Google Scholar 

  • Engberg J, Christiansen G, Leick V (1974) Autonomous rDNA molecules containing single copies of the ribosomal RNA genes in the macronucleus of Tetrahymena pyriformis. Biochem Biophys Res Commun 59: 1356–1365

    PubMed  CAS  Google Scholar 

  • Engberg J, Andersson P, Leick V, Collins J (1976) The free rDNA molecules from Tetrahymena pyriformis GL, are giant palindromes. J Mol Biol 104: 455–470

    PubMed  CAS  Google Scholar 

  • Epstein LM, Forney JD (1984) Mendelian and Non-Mendelian mutations affecting surface antigen expression in Paramecium. Mol Cell Biol 4: 1583–1590

    PubMed  CAS  Google Scholar 

  • Fauré-Fremiet E (1954) Réorganization du type endomixique chez les Loxodidae et chez Centrophorella. J Protozool 1: 20–27

    Google Scholar 

  • Fernandez-Galiano D (1979) Transfer of the widely known “Spirotrich” ciliate, Bursaria truncatella O. F. Müller, to the Vestibulifera as a separate order there, the Bursariomorphida. Trans Am Microsc Soc 98: 447–454

    Google Scholar 

  • Findly RC, Gall JG (1978) Free ribosomal RNA genes in Paramecium are tandemly repeated. Proc Natl Acad Sci USA 75: 3312–3316

    PubMed  CAS  Google Scholar 

  • Findly RC, Gall JG (1980) Organization of ribosomal genes in Paramecium tetraurelia. J Cell Biol 84: 547–549

    PubMed  CAS  Google Scholar 

  • Fujishima M, Watanabe T (1981) Transplantation of germ nuclei in Paramecium caudatum. III. Role of germinal micronucleus in vegetative growth. Exp Cell Res 132: 47–56

    Google Scholar 

  • Forney JD, Epstein LM, Preer LB, Rudman BM, Widmayer DJ, Klein WH, Preer JR (1983) Structure and expression of genes for surface proteins in Paramecium. Mol Cell Biol 3: 466474

    Google Scholar 

  • Gall JG (1974) Free ribosomal RNA genes in the macronucleus of Tetrahymena. Proc Natl Acad Sci USA 71: 3078–3081

    PubMed  CAS  Google Scholar 

  • Gall JG (1981) Chromosome structure and the C-value paradox. J Cell Biol 91: 3s - 14s

    PubMed  CAS  Google Scholar 

  • Gall JG, Yao M-C, Blackburn EH, Findly RC, Wild M (1979) The extrachromosomal ribosomal DNA of Tetrahymena and Paramecium. In: Engberg J, Kleenow H, Leick V (eds) Specific eukaryotic genes. Alfred Benzon Symp, vol 13. Munksgaard, Copenhagen, pp 229–305

    Google Scholar 

  • Gaude H (1981) Zur Funktion der Ciliaten-Riesenchromosomen: Nachweis von RNS-Polymerase in den polytänen Chromosomen der Makronukleusanlage von Stylonychia mytilus. Arch Protistenkd 124: 252–258

    Google Scholar 

  • Gibson I, Martin N (1971) DNA amounts in the nuclei of Paramecium aurelia and Tetrahymena pyriformis. Chromosoma (Berl) 35: 374–382

    Google Scholar 

  • Gillis M, DeLey J, DeCleeve M (1970) The determination of molecular weight of bacterial genome DNA from renaturation rates. Eur J Biochem 12: 143–153

    PubMed  CAS  Google Scholar 

  • Glover CVC, Gorovsky MA (1978) Histone-histone interactions in a lower eukaryote, Tetrahymena. Biochemistry 17: 5705–5713

    Google Scholar 

  • Glover DM, Zaha A, Stocker A.1, Santelli RV, Pueyo MT, DeToledo SM, Lara FJS (1982) Gene amplification in Rhynchosciara salivary gland chromosomes. Proc Natl Acad Sci USA 79: 2947–2951

    CAS  Google Scholar 

  • Golikova MN (1965) Der Aufbau des Kernapparates und die Verteilung der Nukleinsäuren und Proteine bei Nyctotherus cordiformis. Arch Protistenkd 108: 191–216

    CAS  Google Scholar 

  • Gorovsky MA (1973) Macro-and micronuclei of Tetrahymena pyriformis: a model system for studying the structure and function of eukaryotic nuclei. J Protozool 20: 19–25

    PubMed  CAS  Google Scholar 

  • Gorovsky MA (1980) Genome organization and reorganization in Tetrahymena. Annu Rev Genet 14: 203–239

    PubMed  CAS  Google Scholar 

  • Gorovsky MA, Keevert JB (1975) Subunit structure of a naturally occurring chromatin lacking histones F1 and F3. Proc Natl Acad Sci USA 72: 3536–3540

    PubMed  CAS  Google Scholar 

  • Gorovsky MA, Woodard J (1969) Studies on nuclear structure and function in Tetrahymena pyriformis. I. RNA synthesis in macro-and micronuclei. J Cell Biol 42: 673–682

    Google Scholar 

  • Gorovsky MA, Hattman S, Pleger GL (1973) 6N-methyl adenine in the nuclear DNA of a eu-karyote, Tetrahymena pyriformis. J Cell Biol 56: 697–701

    Google Scholar 

  • Gorovsky MA, Keevert JB, Pleger GL (1974) Histone FI of Tetrahymena macronuclei: unique electrophoretic properties and phosphorylation of F’1 in an amitotic nucleus. J Cell Biol 61: 134–145

    PubMed  CAS  Google Scholar 

  • Gorovsky MA, Glover C, Johmann CA, Keevert JB, Mathis DJ, Samuelson M (1978) Histones and chromatin structure in Tetrahymena macro-and micronuclei. Cold Spring Harbor Symp Quant Biol 42: 493–503

    PubMed  CAS  Google Scholar 

  • Grassé P-P (1952) Traité de zoologie, vol 1, fasc I. Masson et Cie, Paris, p 87

    Google Scholar 

  • Grell KG (1949) Die Entwicklung der Makronucleusanlage im Exkonjuganten von Ephelota gemmipara Hertwig. Biol Zentralbl 68: 289–312

    Google Scholar 

  • Grell KG (1953) Die Konjugation von Ephelota gemmipara Hertwig. Arch Protistenkd 98: 287 326

    Google Scholar 

  • Grell KG (1973) Protozoology. Springer, Berlin Heidelberg New York

    Google Scholar 

  • Grell KG (1979) Cytogenetic systems and evolution in Foraminifera. J Foram Res 9:1–13 Hadzi J ( 1963 ) The evolution of the Metazoa. Pergamon, New York

    Google Scholar 

  • Hamana K, Iwai K (1971) Fractionation and characterization of Tetrahymena histone in comparison with mammalian histones. J Biochem (Tokyo) 69: 1097–1111

    CAS  Google Scholar 

  • Hanson ED (1963) Homologies and the ciliate origin of the Eumetazoa. In: Dougherty EC (ed) The lower metazoa. Univ California Press, Berkeley

    Google Scholar 

  • Helftenbein E (1985) Nucleotide sequence of a macronuclear DNA molecule coding for a-tubulin from the ciliate Stylonychia lemnae. Special codon usage: TAA is not a translation termination codon. Nucleic Acids Res 13: 415–433

    PubMed  CAS  Google Scholar 

  • Hennig W (1966) Phylogenetic systematics. Univ Illinois Press, Urbana

    Google Scholar 

  • Hill RJ, Stollar BD (1983) Dependence of Z-DNA antibody binding to polytene chromosomes on acid fixation and DNA torsional strain. Nature (Lond) 305: 338–340

    CAS  Google Scholar 

  • Hutchinson F (1961) Molecular basis for action of ionizing radiations. Science (Wash DC) 134: 533–538

    CAS  Google Scholar 

  • Iwamura Y, Sakai M, Mita T, Muramatsu M (1979) Unequal gene amplification and transcription in the macronucleus of Tetrahymena pyriformis. Biochemistry 18: 5289–5294

    PubMed  CAS  Google Scholar 

  • Iwamura Y, Sakai M, Muramatsu M (1982) Rearrangement of repeated sequences during devel- opment of macronucleus in Tetrahymena thermophila. Nucleic Acids Res 10: 4279–4291

    PubMed  CAS  Google Scholar 

  • Jareno MA, Alonso P, Pérez-Silva J (1972) Identification of some puffed regions in the polytene chromosomes of Stylonychia mytilus. Protistologica 8: 237–243

    Google Scholar 

  • Johmann CA, Gorovsky MA (1976 a) Purification and characterization of the histones associated with the macronucleus of Tetrahymena. Biochemistry 15: 1249–1256

    Google Scholar 

  • Johmann CA, Gorovsky MA (1976 b) An electrophoretic comparison of the histones of various strains of Tetrahymena pyriformis. Arch Biochem Biophys 175: 694–699

    Google Scholar 

  • Kaine BP, Spear BB (1980) Putative actin genes in the macronucleus of Oxytricha fallax. Proc Natl Acad Sci USA 77: 5336–5340

    PubMed  CAS  Google Scholar 

  • Kaine BP, Spear BB (1982) Nucleotide sequence of a macronuclear gene for actin in Oxytricha fallax. Nature (Lond) 295: 430–432

    CAS  Google Scholar 

  • Kaney AR, Speare VJ (1983) An amicronucleate mutant of Tetrahymena thermophila. Exp Cell Res 143: 461–467

    PubMed  CAS  Google Scholar 

  • Karrer KM (1983) Germ line-specific DNA sequences are present on all five micronuclear chromosomes in Tetrahymena thermophila. Mol Cell Biol 3: 1909–1919

    PubMed  CAS  Google Scholar 

  • Karrer K, Gall J (1975) The macronuclear ribosomal DNA of Tetrahymena is a palindrome. J Cell Biol 67:202 a

    Google Scholar 

  • Karrer K, Gall J (1976) The macronuclear ribosomal DNA of Tetrahymena is a palindrome. J Mol Biol 104: 421–453

    PubMed  CAS  Google Scholar 

  • Karrer K, Stein-Gavens S, Allitto BA (1984) Micronucleus-specific DNA sequences in an amicronucleate mutant of Tetrahymena. Dev Biol 105: 121–129

    PubMed  CAS  Google Scholar 

  • Katzen AL, Cann GM, Blackburn EH (1981) Sequence-specific fragmentation of macronuclear DNA in a holotrichous ciliate. Cell 24: 313–320

    PubMed  CAS  Google Scholar 

  • Kavenoff R, Zimm BH (1973) Chromosome-sized DNA molecules from Drosophila. Chromo-soma (Berl) 41: 1–27

    CAS  Google Scholar 

  • Kimmel AR, Gorovsky MA (1976) Numbers of 5S and tRNA genes in macro-and micronuclei of Tetrahymena pyriformis. Chromosoma (Berl) 54: 327–337

    CAS  Google Scholar 

  • King BO, Yao M-C (1982) Tandemly repeated hexanucleotide at Tetrahymena rDNA free end is generated from a single copy during development. Cell 31: 177–182

    PubMed  CAS  Google Scholar 

  • Kiss GB, Amin AA, Pearlman RE (1981) Two separate regions of the extrachromosomal ribosomal deoxyribonucleic acid of Tetrahymena thermophila enable autonomous replication of plasmids in Saccharomyces cerevisiae. Mol Cell Biol 1: 535–543

    PubMed  CAS  Google Scholar 

  • Klobutcher LA, Swanton MT, Donini P, Prescott DM (1981) All gene-sized DNA molecules in four species of hypotrichs have the same terminal sequence and an unusual 3’terminus. Proc Natl Acad Sci USA 78: 3015–3019

    PubMed  CAS  Google Scholar 

  • Klobutcher LA, Jahn CL, Prescott DM (1984) Internal sequences are eliminated from genes during macronuclear development in the ciliated protozoan, Oxytricha nova. Cell 36: 10451055

    Google Scholar 

  • Kloetzel JA (1970) Compartmentalization of the developing macronucleus following conjugation in Stylonychia and Euplotes. J Cell Biol 47: 395–407

    PubMed  CAS  Google Scholar 

  • Kovaleva VG, Raikov IB (1973) Ultrastructure de l’appareil nucléaire de Trachelonema sulcata Kovaleva, Cilié holotriche gymnostome à macronoyaux diploides. Protistologica 9: 471480

    Google Scholar 

  • Kovaleva VG, Raikov IB (1978) Diminution and re-synthesis of DNA during development and senescence of the “diploid” macronuclei of the ciliate Trachelonema sulcata ( Gymnostomata, Karyorelictida). Chromosoma (Berl ) 67: 177–192

    Google Scholar 

  • Lauth MR, Spear BB, Heumann J, Prescott DM (1976) DNA of ciliated protozoa: DNA se-quence diminution during macronuclear development of Oxytricha. Cell 7: 67–74

    Google Scholar 

  • Lawn RM, Heumann JM, Herrick G, Prescott DM (1978) The gene-sized DNA molecules of Oxytricha. Cold Spring Harbor Symp Quant Biol 42: 483–492

    PubMed  CAS  Google Scholar 

  • Lee G-S, Lewis SA, Wilde CD, Cowan NJ (1983) Evolutionary history of a multigene family: an expressed human a-tubulin and three processed pseudogenes. Cell 33: 477–487

    PubMed  CAS  Google Scholar 

  • Levine ND, Corliss JO, Cox FEG, Deroux G, Grain J, Honigberg BM, Leedale GF, Loeblich III AR, Lom J, Lynn D, Merinfeld EG, Page FC, Poljansky G, Sprague V, Vavra J, Wallace FG (1980) A newly revised classification of the Protozoa. J Protozool 27: 37–58

    PubMed  CAS  Google Scholar 

  • Lipps HJ (1980) In vitro aggregation of the gene-sized DNA molecules of the ciliate, Stylonychia mytilus. Proc Natl Acad Sci USA 77: 4104–4107

    PubMed  CAS  Google Scholar 

  • Lipps HJ, Erhard P (1981) DNase I hypersensitivity of the terminal inverted repeat DNA se-quences in the macronucleus of the ciliate, Stylonychia mytilus. FEBS Lett 126: 219–222

    Google Scholar 

  • Lipps HJ, Hantke KG (1975) Studies on the histones of the ciliate, Stylonychia mytilus. Chro-mosoma (Berl) 49: 309–320

    Google Scholar 

  • Lipps HJ, Morris NR (1977) Chromatin structure in the nuclei of the ciliate, Stylonychia mytilus. Biochem Biophys Res Commun 74: 230–234

    Google Scholar 

  • Lipps HJ, Steinbrück G (1978) Free genes for rRNAs in the macronuclear genome of the ciliate, Stylonychia mytilus. Chromosoma (Berl) 69: 21–26

    Google Scholar 

  • Lipps HJ, Sapra GR, Ammermann D (1974) The histones of the ciliated protozoan, Stylonychia mytilus. Chromosoma (Berl) 45: 273–280

    Google Scholar 

  • Lipps HJ, Nordheim A, Lafer EM, Ammermann D, Stollar BD, Rich A (1983) Antibodies against Z DNA react with the macronucleus but not the micronucleus of the hypotrichous ciliate, Stylonychia mytilus. Cell 32: 435–441

    Google Scholar 

  • Lipscombe DL, Corliss JO (1982) Stephanopogon, a phylogenetically important “ciliate”, shown by ultrastructural studies to be a flagellate. Science (Wash DC) 215: 303–304

    Google Scholar 

  • Lwoff A (1923) Sur la nutrition des infusoires. C R Acad Sci Paris 176: 928–930

    CAS  Google Scholar 

  • Mayr E (1963) Animal species and evolution. The Belknap Press of Harvard Univ Press, Cambridge, Mass

    Google Scholar 

  • McCoy (1976) Updating the tetrahymenids. II. Domestic and natural variation of amicronu-cleate species of the Tetrahymena pyriformis complex. Acta Protozool 13: 235–243

    Google Scholar 

  • McTavish C, Sommerville J (1980) Macronuclear DNA organization and transcription in Para-mecium primaurelia. Chromosoma (Berl) 78: 147–164

    CAS  Google Scholar 

  • Merkulova NA, Borchsenius SN (1976) Replication and integration of fragments of new chains into the DNA of the ciliate, Tetrahymena pyriformis GL. Mol Biol (Mosc) 10: 1072–1077 (in Russian with English summary)

    Google Scholar 

  • Meyer GF, Lipps HJ (1980) Chromatin elimination in the hypotrichous ciliate, Stylonychia mytilus. Chromosoma (Berl) 77: 285–297

    Google Scholar 

  • Meyer GF, Lipps HJ (1981) The formation of polytene chromosomes during macronucleus development of the hypotrichous ciliate, Stylonychia mytilus. Chromosoma (Berl) 82: 309314

    Google Scholar 

  • Meyer GF, Lipps HJ (1984) Electron microscopy of surface spread polytene chromosomes of Drosophila and Stylonychia. Chromosoma (Berl) 89: 107–110

    Google Scholar 

  • Mikami K, Kuhlmann H-W, Heckmann K (1985) Is the initiation of macronuclear DNA syn- thesis in Euplotes dependent on micronuclear functions?

    Google Scholar 

  • J Protozool in press Möhn E (1984) System und Phylogenie der Lebewesen, vol 1. Schweizerbart, Stuttgart

    Google Scholar 

  • Murti KG, Prescott DM (1970) Micronuclear ribonucleic acid in Tetrahymena pyriformis. J Cell Biol 47: 460–467

    PubMed  CAS  Google Scholar 

  • Murti KG, Prescott DM (1983) Replication forms of the gene-sized DNA molecules of hypotrichous ciliates. Mol Cell Biol 3: 1562–1566

    PubMed  CAS  Google Scholar 

  • Nanney DL (1964) Macronuclear differentiation and subnuclear assortment in ciliates. In: Locke M (ed) The role of chromosomes in development. Academic Press, New York, pp 253–273 Nanney DL ( 1980 ) Experimental ciliatology. Wiley, New York

    Google Scholar 

  • Nanney DL, McCoy JW (1976) Characterization of the species of the Tetrahymena pyriformis complex. Trans Am Micros Soc 95: 664–682

    CAS  Google Scholar 

  • Nanney DL, Preparata RM (1979) Genetic evidence concerning the structure of the Tetrahymena thermophila macronucleus. J Protozool 26: 2–9

    Google Scholar 

  • Nasmyth KA (1982) Molecular genetics of yeast mating type. Annu Rev Genet 16: 439–500

    PubMed  CAS  Google Scholar 

  • Ng SF, Newman A (1984) The role of the micronucleus in stomatogenesis in sexual reproduction of Paramecium tetraurelia: Micronuclear and stomatogenic events. Protistologica 20: 43–64

    Google Scholar 

  • Nock A (1981) RNA and macronuclear transcription in the ciliate, Stylonychia mytilus. Chro-mosoma (Berl) 83: 209–220

    CAS  Google Scholar 

  • Nouzarède M (1976) Cytology fonctionelle et morphologie expérimentale de quelques Protozoaires ciliés mésopsammique géant de la famille des Geleiidae (Kahl). Bull State Biol Arcachon (Suppl) NS 28: 1–315

    Google Scholar 

  • Ohama T, Kumazaki T, Hori H, Osawa S (1984) Evolution of multicellular animals as deduced from 5S rRNA sequences: a possible early emergence of the Mesozoa. Nucleic Acids Res 12: 5101–5108

    PubMed  CAS  Google Scholar 

  • Oka Y, Honjo T (1983) Common terminal repeats of the macronuclear DNA are absent from the micronuclear DNA in hypotrichous ciliate, Stylonychia pustulata. Nucleic Acids Res 11: 4325–4333

    Google Scholar 

  • Oka Y, Shiota S, Nakai S, Nishida Y, Okulbo S (1980) Inverted terminal repeat sequences in the macronuclear DNA of Stylonychia pustulata. Gene (Amst) 10: 301–306

    CAS  Google Scholar 

  • Orgel LE, Crick FHC (1980) Selfish DNA: the ultimate parasite. Nature (Lond) 284:604–607 Orgel LE, Crick FHC, Sapienza C (1980) Selfish DNA. Nature (Lond) 288: 645–646

    CAS  Google Scholar 

  • Orias E (1981) Probable somatic DNA rearrangements in mating type determination in Tetra-hymena thermophila: a review and a model. Dev Genet 2: 185–202

    CAS  Google Scholar 

  • Orias E, Flacks M (1975) Macronuclear genetics of Tetrahymena. I. Random distribution of macronuclear gene copies in Tetrahymena pyriformis syngen 1. Genetics 79: 187–206

    PubMed  CAS  Google Scholar 

  • Pan W-C, Blackburn EH (1981) Single extrachromosomal ribosomal RNA gene copies are syn-thesized during amplification of the rDNA in Tetrahymena. Cell 23: 459–466

    PubMed  CAS  Google Scholar 

  • Pan WC, Orias E, Flacks M, Blackburn EH (1982) Allele-specific selective amplification of a ri-bosomal RNA gene in Tetrahymena thermophila. Cell 28: 595–604

    PubMed  CAS  Google Scholar 

  • Pasternak J (1967) Differential genic activity in Paramecium aurelia. J Exp Zool 165:395–417 Pavan C, DaCunha AB (1969) Chromosomal activities in Rhynchosciara and other Sciaridae. Annu Rev Genet 3: 425–450

    Google Scholar 

  • Pelvat B, DeHaller G (1976) Macronuclear DNA in Stentor coeruleus: a first approach to its characterization. Genet Res 27: 277–289

    PubMed  CAS  Google Scholar 

  • Pérez-Silva J, Alonso P (1966) Demonstration of polytene chromosomes in the macronuclear anlage of Oxytrichous ciliates. Arch Protistenkd 109: 65–70

    Google Scholar 

  • Pluta AF, Kaine BP, Spear BB (1982) The terminal organization of macronuclear DNA in Oxytricha fallax. Nucleic Acids Res 10: 8145–8154

    PubMed  CAS  Google Scholar 

  • Pluta AF, Dani GM, Spear BB, Zakian VA (1984) Elaboration of telomers in yeast: recognition and modification of termini from Oxytricha macronuclear DNA. Proc Natl Acad Sci USA 81: 1475–1479

    PubMed  CAS  Google Scholar 

  • Poljansky G (1933/34) Geschlechtsprozesse bei Bursaria truncatella O. F. Müller. Arch Protistenkd 81: 420–546

    Google Scholar 

  • Poljansky G, Sergejeva GI (1981) Autoradiographic investigation of the DNA synthesis during development of the new macronucleus of the ciliate Bursaria truncatella. Tsitologiya 23: 666673 (in Russian with English summary)

    Google Scholar 

  • Preer JR Jr (1969) Genetics of Protozoa. In: Chen TT (ed) Research in protozoology. Pergamon, Oxford, pp 139–288

    Google Scholar 

  • Preer JB, Preer LB (1979) The size of macronuclear DNA and its relation to models for maintaining genetic balance. J Protozool 26: 14–18

    CAS  Google Scholar 

  • Prescott DM (1983) The C-value paradox and genes in ciliated protozoa. Mod Cell Biol 2: 329352

    Google Scholar 

  • Prescott DM, Murti KG, Bostock CJ (1973) Genetic apparatus of Stylonychia sp. Nature (Lond) 242: 597–600

    Google Scholar 

  • Prescott DM, Bostock CJ, Murti KG, Lauth MR, Gamow E (1971) DNA of ciliated protozoa. I. Electron microscopic and sedimentation analyses of macronuclear and micronuclear DNA of Stylonychia mytilus. Chromosoma (Berl) 34: 355–366

    Google Scholar 

  • Prescott DM, Heumann JM, Swanton M, Boswell RE (1979) The genome of hypotrichous ciliates. In: Engberg I, Kleenow H, Leick V (eds) Specific eukaryotic genes. Alfred Benzon Symp, vol 13. Munksgaard, Copenhagen, pp 85–99

    Google Scholar 

  • Proudfoot N (1980) Pseudogenes. Nature (Lond) 286: 840–841

    CAS  Google Scholar 

  • Pyne CK (1978) Electron microscopic studies on the macronuclear development in the ciliate, Chilodonella uncinata. Cytobiologie 18: 145–160

    PubMed  CAS  Google Scholar 

  • Pyne CK, Ruch F, Leemann U, Schneider S (1974) Development of the macronuclear anlage in the ciliate Chilodonella uncinata. Chromosoma (Berl) 48: 225–238

    CAS  Google Scholar 

  • Radzikowski S (1973) Die Entwicklung des Kernapparates and die Nukleinsäuresynthese während der Konjugation von Chilodonella cucullulus O. F. Müller. Arch Protistenkd 115: 419428

    Google Scholar 

  • Radzikowski S (1976) DNA and RNA synthesis in the nuclear apparatus of Chilodonella cucul-lulus O. F. M üller. Acta Protozool 15: 47–56

    CAS  Google Scholar 

  • Radzikowski S (1979) Asynchronous replication of polytene chromosome segments of the new macronucleus anlage in Chilodonella cucullulus O. F. Müller. Protistologica 15: 521–526

    CAS  Google Scholar 

  • Radzikowski S, Golembiewska M (1977) Chilodonella steini. Morphology and culture method. Protistologica 13: 381–389

    Google Scholar 

  • Rae PMM, Spear BB (1978) Macronuclear DNA of the hypotrichous ciliate Oxytricha fallax. Proc Natl Acad Sci USA 75: 4992–4996

    PubMed  CAS  Google Scholar 

  • Rae PMM, Steele RE (1978) Modified bases in the DNAs of unicellular eukaryotes: an examination of distributions and possible roles, with emphasis on hydroxymethylcytosine. Biosystems 10: 37–53

    PubMed  CAS  Google Scholar 

  • Raikov IB (1959) Der Formwechsel des Kernapparates einiger niederer Ciliaten. II. Die Gattung Loxodes. Arch Protistenkd 104: 1–42

    Google Scholar 

  • Raikov IB (1969) The macronucleus of ciliates. In: Chen T-T (ed) Research in protozoology, vol 3. Pergamon, Oxford, pp 1–128

    Google Scholar 

  • Raikov IB (1972) Ultrastructure des „capsule nucléaires“ („noyaux composés”) du Cilié psammophile Kentrophoros latum Raikov 1962. Protistologica 8: 299–313

    Google Scholar 

  • Raikov IB (1976) Evolution of macronuclear organization. Annu Rev Genet 10:41340 Raikov IB ( 1982 ) The protozoan nucleus. Springer, Berlin Heidelberg New York

    Google Scholar 

  • Raikov IB, Dragesco J (1969) Ultrastructure des noyaux et de quelques organites cytoplasmiques

    Google Scholar 

  • du cilié Tracheloraphis caudatum Dragesco et Raikov (Holotricha, Gymnostomatida). Pro-tistologica 5: 193–208

    Google Scholar 

  • Raikov IB, Morat G (1977) Etude autoradiographique de la synthèse de l’ADN et de l’ARN dans les noyaux du Cilié Loxodes magnus Stokes. Protistologica 13: 391–399

    CAS  Google Scholar 

  • Rao MVN, Ammermann D (1970) Polytene chromosomes and nucleic acid metabolism during macronuclear development in Euplotes. Chromosoma (Berl) 29: 246–254

    CAS  Google Scholar 

  • Rao MVN, Prescott DM (1967) Micronuclear RNA synthesis in Paramecium caudatum. J Cell Biol 33: 281–285

    CAS  Google Scholar 

  • Remane A (1952) Die Besiedlung des Sandbodens im Meere und die Bedeutung der Lebensform-typen für die Ökologie. Verh Dtsch Zool Ges 1951: 327–359

    Google Scholar 

  • Ron A, Urieli S (1977) Qualitative and quantitative studies on DNA and RNA synthesis in Loxodes striatus nuclei. J Protozool 24: 150–154

    PubMed  CAS  Google Scholar 

  • Ruthmann A (1964) Autoradiographische und mikrophotometrische Untersuchungen zur

    Google Scholar 

  • DNA-Synthese im Makronucleus von Bursaria truncatella. Arch Protistenkd 107:117–130

    Google Scholar 

  • Ruthmann A (1972) Division and formation of the macronuclei of Keronopsis rubra. J Pro-tozool 19: 661–666

    Google Scholar 

  • Schlegel M (1985) Comparative study of allzyme variation in eight species of hypotrichous cili-ates (Polyhymenophora, Ciliophora). Zool Syst u Evolut-Forsch 23: 171–183

    Google Scholar 

  • Schwartz V (1958) Chromosomen im Makronucleus von Paramecium bursaria. Biol Zentralbl 77: 347–364

    Google Scholar 

  • Schwartz V, Meister H (1975) Die Extinktion der feulgengefärbten Makronucleusanlage von Paramecium bursaria in der DNA-armen Phase. Arch Protistenkd 117: 60–64

    CAS  Google Scholar 

  • Seyffert H-M (1979) Evidence for chromosomal macronuclear substructures in Tetrahymena. J Protozool 26: 66–74

    Google Scholar 

  • Soldo AT, Brickson SA, Lavin F (1981) The kinetic and analytical complexities of the DNA genomes of certain marine and fresh water ciliates. J Protozool 28: 377–383

    CAS  Google Scholar 

  • Sommerville J (1970) Serotype expression in Paramecium. Adv Microb Physiol 4: 131–178

    Google Scholar 

  • Sonneborn TM (1957) Breeding systems, reproductive methods and species problems in Pro-tozoa. In: Mayr E (ed) The species problem. Am Assoc Adv Sci Publ, Washington, pp 155–324

    Google Scholar 

  • Sonneborn TM ( 1974 a) Paramecium aurelia. In: King RC (ed) Handbook of genetics, vol 2. Plenum, New York, pp 469–594

    Google Scholar 

  • Sonneborn TM ( 1974 b) Tetrahymena pyriformis. In: King RC (ed) Handbook of genetics, vol 2. Plenum, New York, pp 433–467

    Google Scholar 

  • Sonneborn TM (1975) The Paramecium aurelia complex of 14 sibling species. Trans Am Micros Soc 94: 155–178

    Google Scholar 

  • Spear BB (1980) Isolation and mapping of the rRNA genes in the macronucleus of Oxytricha fallax. Chromosoma (Berl) 77: 93–202

    Google Scholar 

  • Spear BB, Lauth MR (1976) Polytene chromosomes of Oxytricha: biochemical and morphological changes during macronuclear development in a ciliated protozoan. Chromosoma (Berl) 54: 1–13

    CAS  Google Scholar 

  • Steinböck 0 (1963) Origin and affinities of the Lower Metazoa: The “Aceloid” ancestry of the Eumetazoa. In: Dougherty EC (ed) The Lower Metazoa. Univ California Press, Berkeley

    Google Scholar 

  • Steinbrück G (1976) Untersuchungen zur Organisation des Genomes von Stylonychia mytilus ( Ciliata ). Thesis Univ Tübingen

    Google Scholar 

  • Steinbrück G (1983) Overamplification of genes in macronuclei of hypotrichous ciliates. Chromosoma (Berl) 88: 156–163

    Google Scholar 

  • Steinbrück G, Schlegel M (1983) Characterization of two sibling species of the genus Stylonychia (Ciliata, Hypotricha): S. mytilus Ehrenberg, 1838 and S. lemnae n. sp. II. Biochemical characterization. J Protozool 30: 294–300

    Google Scholar 

  • Steinbrück G, Haas I, Hellmer K-H, Ammermann D (1981) Characterization of macronuclear DNA in five species of ciliates. Chromosoma (Berl) 83: 199–208

    Google Scholar 

  • Sugai T, Hiwatashi K (1974) Cytologic and autoradiographic studies of the micronucleus at meiotic prophase in Tetrahymena pyriformis. J Protozool 21: 542–548

    PubMed  CAS  Google Scholar 

  • Swanton MT, Heumann JM, Prescott DM (1980 b) Gene-sized molecules of the macronuclei in three species of hypotrichs: size distribution and absence of nicks. Chromosoma (Berl) 77: 217–227

    Google Scholar 

  • Swanton MT, McCarroll RM, Spear BB (1982) The organization of macronuclear rDNA molecules of four hypotrichous ciliated protozoans. Chromosoma (Berl) 85: 1–9

    CAS  Google Scholar 

  • Szostak JW, Blackburn EH (1982) Cloning yeast telomeres on linear plasmid vectors. Cell 29: 245–255

    PubMed  CAS  Google Scholar 

  • Tait A (1970) Enzyme variation between syngens in Paramecium aurelia. Biochem Genet 4: 461470

    Google Scholar 

  • Toennesen T, Engberg J, Leick V (1976) Studies on the amount and the localization of the tRNA and 5-S rRNA genes in Tetrahymena pyriformis GL. Eur J Biochem 63: 399–407

    CAS  Google Scholar 

  • Tonegawa S (1983) Somatic generation of antibody diversity. Nature (Lond) 302: 575–581

    CAS  Google Scholar 

  • Torch R (1964) Autoradiographic studies of nucleic acid synthesis in a gymnostome ciliate, Tra-cheloraphis sp. J Cell Biol 23:98 a

    Google Scholar 

  • Truett MA, Gall JG (1977) The replication of ribosomal DNA in the macronucleus of Tetrahymena. Chromosoma (Berl) 64: 295–303

    CAS  Google Scholar 

  • Vorob’ev VI, Borchsenius SM, Belozerskaya NA, Merkulova NA, Irlina IS (1975) DNA repli-cation in macronuclei of Tetrahymena pyriformis GL. Exp Cell Res 93: 253–260

    PubMed  Google Scholar 

  • Wells C (1960) The response of Tetrahymena pyriformis to ionizing radiation: strain specific radiosensitivities. J Cell Comp Physiol 55: 207–219

    PubMed  CAS  Google Scholar 

  • Werz G (1974) Fine structural aspects of morphogenesis in Acetabularia. Int Rev Cytol 30: 319367

    Google Scholar 

  • Wesley RD (1975) Inverted repetitious sequences in the macronuclear DNA of hypotrichous ciliates. Proc Natl Acad Sci USA 72: 678–682

    PubMed  CAS  Google Scholar 

  • Williams JB, Fleck EW, Hellier LE, Uhlenhopp E (1978) Viscoelastic studies on Tetrahymena macronuclear DNA. Proc Natl Acad Sci USA 75: 5062–5065

    PubMed  CAS  Google Scholar 

  • White T, Allen S (1984) Eliminated sequences and a specific site of methylation in the macronucleus of Tetrahymena thermophila. In: Abstracts of papers presented at the meeting on “Ciliate molecular genetics” 2.5.-6.5. 1984. Cold Spring Harbor Laboratory, New York, p 11

    Google Scholar 

  • Wild MA, Gall JG (1979) An intervening sequence in the gene coding for 25S ribosomal RNA of Tetrahymena pigmentosa. Cell 16: 565–573

    PubMed  CAS  Google Scholar 

  • Wollgiehn R (1982) Control of morphogenesis in Acetabularia. In: Nover L, Luckner M, Par-thier B (eds) Cell differentiation. Springer, Berlin Heidelberg New York, pp 529–548

    Google Scholar 

  • Woodard J, Kaneshiro E, Gorovsky MA (1972) Cytochemical studies on the problem of mac-ronuclear subnuclei in Tetrahymena. Genetics 70: 251–260

    PubMed  CAS  Google Scholar 

  • Wünning IU, Lipps HJ (1983) A transformation system for the hypotrichous ciliate, Stylonychia mytilus. EM BO J 2: 1753–1757

    Google Scholar 

  • Yao M-C (1981) Ribosomal RNA gene amplification in Tetrahymena may be associated with chromosome breakage and DNA elimination. Cell 24: 765–774

    PubMed  CAS  Google Scholar 

  • Yao M-C (1982 a) Elimination of specific DNA sequences from the somatic nucleus of the ciliate, Tetrahymena. J Cell Biol 92: 783–789

    Google Scholar 

  • Yao M-C ( 1982 b) Amplification of ribosomal RNA genes in Tetrahymena. In: Busch H, Rothblum L (eds) The cell nucleus. Academic, New York, pp 127–153

    Google Scholar 

  • Yao M-C, Gall JG (1977) A single integrated gene for ribosomal RNA in a eucaryote, Tetrahymena pyriformis. Cell 12: 121–132

    Google Scholar 

  • Yao M-C, Gorovsky MA (1974) Comparison of the sequences of macro-and micronuclear DNA of Tetrahymena pyriformis. Chromosoma (Berl) 48: 1–18

    CAS  Google Scholar 

  • Yao M-C, Yao CH (1981) The repeaed hexanucleotide C-C-C-C-A-A is present near free ends

    Google Scholar 

  • of macronuclear DNA of Tetrahymena. Proc Natl Acad Sci USA 78:7436–7439

    Google Scholar 

  • Yao M-C, Blackburn E, Gall JG (1979) Amplification of rRNA genes in Tetrahymena. Cold

    Google Scholar 

  • Spring Harbor Symp Quant Biol 43:1293–1296

    Google Scholar 

  • Yao M-C, Blackburn E, Gall JG (1981) Tandemly repeated C-C-C-C-A-A hexanucleotide of Tetrahymena rDNA is present elsewhere in the genome and may be related to the alteration of the somatic genome. J Cell Biol 90: 515–520

    PubMed  CAS  Google Scholar 

  • Yao M-C, Kimmel AR, Gorovsky MA (1974) A small number of cistrons for ribosomal RNA in the germinal nucleus of a eukaryote, Tetrahymena pyriformis. Proc Natl Acad Sci USA 71: 3082–3086

    Google Scholar 

  • Yao M-C, Choi J, Yokoyama S, Austerberry CF, Yao C-H (1984) DNA elimination in Tetra-hymena: a developmental process involving extensive breakage and rejoining of DNA at defined sites. Cell 36: 433–440

    PubMed  CAS  Google Scholar 

  • Yokoyama RW, Yao M-C (1982) Elimination of DNA sequences during macronuclear differentiation in Tetrahymena thermophila as detected by in situ hybridization. Chromosoma (Berl) 85: 11–22

    CAS  Google Scholar 

  • Zech L (1964) Zytochemische Messungen an den Zellkernen der Foraminiferen, Patellina corrugata and Rotaliella heterokaryotica. Arch Protistenkd 107: 295–330

    Google Scholar 

  • Zier H (1972) Cytologische Untersuchungen zur Konjugation von Euplotes aediculatus. Thesis Univ Münster

    Google Scholar 

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Steinbrück, G. (1986). Molecular Reorganization During Nuclear Differentiation in Ciliates. In: Hennig, W. (eds) Germ Line — Soma Differentiation. Results and Problems in Cell Differentiation, vol 13. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-540-39838-7_3

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