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. 1973 Feb 1;56(2):441–457. doi: 10.1083/jcb.56.2.441

REGULATION OF MICROTUBULES IN TETRAHYMENA

I. Electron Microscopy of Oral Replacement

Norman E Williams 1, Joseph Frankel 1
PMCID: PMC2108907  PMID: 4345553

Abstract

The coupled resorption and redifferentiation of oral structures which occurs in Tetrahymena pyriformis under conditions of amino acid deprivation has been studied by transmission electron microscopy. Two patterns of ciliary resorption have been found, (a) in situ, and (b) after withdrawal into the cytoplasm. No autophagic vacuoles containing cilia or ciliary axonemes have been seen. Stomatogenic field basal bodies arise by a process of rapid sequential nucleation, with new ones always appearing next to more mature ones, even though the latter may not be fully differentiated. Accessory radial ribbons of microtubules develop immediately adjacent to oral field basal bodies as a late step in their maturation. It can be seen that the formation of basal bodies and their orientation within the oral complex are separate processes. This is true for about 130 of the approximately 170 oral basal bodies; the remaining 40 or so form within the patterned groups of ciliary units as a later event. Clusters of randomly oriented thin-walled microtubules are found surrounding oral basal bodies at all times during stomatogenesis. They may either represent stores of microtubule subunit protein, or serve as effectors of basal body movement during their orientation into pattern.

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Selected References

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

  1. Allen R. D. The morphogenesis of basal bodies and accessory structures of the cortex of the ciliated protozoan Tetrahymena pyriformis. J Cell Biol. 1969 Mar;40(3):716–733. doi: 10.1083/jcb.40.3.716. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Dippell R. V. The development of basal bodies in paramecium. Proc Natl Acad Sci U S A. 1968 Oct;61(2):461–468. doi: 10.1073/pnas.61.2.461. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Dirksen E. R. Centriole morphogenesis in developing ciliated epithelium of the mouse oviduct. J Cell Biol. 1971 Oct;51(1):286–302. doi: 10.1083/jcb.51.1.286. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Forer A., Nilsson J. R., Zeuthen E. Studies on the oral apparatus of Tetrahymena pyriformis Gl. C R Trav Lab Carlsberg. 1970;38(4):67–86. [PubMed] [Google Scholar]
  5. Frankel J. Participation of the undulating membrane in the formation of oral replacement primordia in Tetrahymena pyriformis. J Protozool. 1969 Feb;16(1):26–35. doi: 10.1111/j.1550-7408.1969.tb02228.x. [DOI] [PubMed] [Google Scholar]
  6. Frankel J. The effect of nucleic acid antagonists on cell division and oral organelle development in Tetrahymena pyriformis. J Exp Zool. 1965 Jun;159(1):113–147. doi: 10.1002/jez.1401590109. [DOI] [PubMed] [Google Scholar]
  7. Frisch D., Farbman A. I. Development of order during ciliogenesis. Anat Rec. 1968 Oct;162(2):221–232. doi: 10.1002/ar.1091620209. [DOI] [PubMed] [Google Scholar]
  8. Johnson U. G., Porter K. R. Fine structure of cell division in Chlamydomonas reinhardi. Basal bodies and microtubules. J Cell Biol. 1968 Aug;38(2):403–425. doi: 10.1083/jcb.38.2.403. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Kormos J. Two types of ciliary resorption. Acta Biol Acad Sci Hung. 1971;22(3):245–260. [PubMed] [Google Scholar]
  10. LUFT J. H. Improvements in epoxy resin embedding methods. J Biophys Biochem Cytol. 1961 Feb;9:409–414. doi: 10.1083/jcb.9.2.409. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Levy M. R., Elliott A. M. Biochemical and ultrastructural changes in Tetrahymena pyriformis during starvation. J Protozool. 1968 Feb;15(1):208–222. doi: 10.1111/j.1550-7408.1968.tb02113.x. [DOI] [PubMed] [Google Scholar]
  12. Nilsson J. R., Williams N. E. An electron microscope study of the oral apparatus of Tetrahymena pyriformis. C R Trav Lab Carlsberg. 1966;35(7):119–141. [PubMed] [Google Scholar]
  13. Paulin J. J., Bussey J. Oral regeneration in the ciliate Stentor coeruleus: a scanning and transmission electron optical study. J Protozool. 1971 May;18(2):201–213. doi: 10.1111/j.1550-7408.1971.tb03308.x. [DOI] [PubMed] [Google Scholar]
  14. ROTH L. E., SHIGENAKA Y. THE RESORPTION OF CILIA. Z Zellforsch Mikrosk Anat. 1964 Sep 17;64:19–24. doi: 10.1007/BF00339181. [DOI] [PubMed] [Google Scholar]
  15. Tucker J. B. Spatial discrimination in the cytoplasm during microtubule morphogenesis. Nature. 1971 Aug 6;232(5310):387–389. doi: 10.1038/232387a0. [DOI] [PubMed] [Google Scholar]
  16. Williams N. E., Luft J. H. Use of a nitrogen mustard derivative in fixation for electron microscopy and observations on the ultrastructure of Tetrahymena. J Ultrastruct Res. 1968 Nov;25(3):271–292. doi: 10.1016/s0022-5320(68)80074-7. [DOI] [PubMed] [Google Scholar]
  17. Williams N. E., Nelsen E. M. Regulation of microtubules in Tetrahymena. II. Relation between turnover of microtubule proteins and microtubule dissociation and assembly during oral replacement. J Cell Biol. 1973 Feb;56(2):458–465. doi: 10.1083/jcb.56.2.458. [DOI] [PMC free article] [PubMed] [Google Scholar]

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