Abstract
Although somatic tissues of Sciara contain 9-membered centrioles, germ line tissues develop giant centrioles with 60–90 singlet tubules disposed in an oval array. Some 9-membered centrioles still may be seen in second instar spermatogonia. Each of these centrioles is associated with a larger "daughter" or secondary centriole at right angles to it. Most centrioles of second instar spermatogonia consist of 20–50 singlet tubules arranged in an oval, sometimes associated with an even larger secondary centriole. The more recently formed centriole of a pair is distinguishable from its partner by a concentric band of electron-opaque material inside its tubules. If a pair of centrioles at right angles to each other is pictured as a "T" formed by two cylinders, the secondary centriole is always the stem of the T; the primary centriole is the top. The two centrioles are oriented at the pole of the mitotic spindle so that the tubules of the primary centriole are parallel to the spindle axis. Each daughter cell receives a pair of centrioles and, during interphase, each of these centrioles gives rise to a new daughter centriole. A Golgi area of characteristic morphology is found in association with centrioles shortly after two new ones have formed. We conclude that in Sciara a centriole may give rise to a daughter morphologically different from itself. Whether the daughter is a 9-membered or giant centriole depends on the tissue type and stage of development.
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Selected References
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- ARGETSINGER J. THE ISOLATION OF CILIARY BASAL BODIES (KINETOSOMES) FROM TETRAHYMENA PYRIFORMIS. J Cell Biol. 1965 Jan;24:154–157. doi: 10.1083/jcb.24.1.154. [DOI] [PMC free article] [PubMed] [Google Scholar]
- FAWCETT D. W. The fine structure of chromosomes in the meiotic prophase of vertebrate spermatocytes. J Biophys Biochem Cytol. 1956 Jul 25;2(4):403–406. doi: 10.1083/jcb.2.4.403. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Friedländer M., Wahrman J. Giant centrioles in neuropteran meiosis. J Cell Sci. 1966 Mar;1(1):129–144. doi: 10.1242/jcs.1.1.129. [DOI] [PubMed] [Google Scholar]
- GABRUSEWYCZ-GARCIA N. CYTOLOGICAL AND AUTORADIOGRAPHIC STUDIES IN SCIARA COPROPHILA SALIVARY GLAND CHROMOSOMES. Chromosoma. 1964 Aug 14;15:312–344. doi: 10.1007/BF00321517. [DOI] [PubMed] [Google Scholar]
- GALL J. G. Centriole replication. A study of spermatogenesis in the snail Viviparus. J Biophys Biochem Cytol. 1961 Jun;10:163–193. doi: 10.1083/jcb.10.2.163. [DOI] [PMC free article] [PubMed] [Google Scholar]
- HAWKER L. E. FINE STRUCTURE OF FUNGI AS REVEALED BY ELECTRON MICROSCOPY. Biol Rev Camb Philos Soc. 1965 Feb;40:52–92. doi: 10.1111/j.1469-185x.1965.tb00795.x. [DOI] [PubMed] [Google Scholar]
- HOFFMAN E. J. THE NUCLEIC ACIDS OF BASAL BODIES ISOLATED FROM TETRAHYMENA PYRIFORMIS. J Cell Biol. 1965 May;25:217–228. doi: 10.1083/jcb.25.2.217. [DOI] [PMC free article] [PubMed] [Google Scholar]
- KRISHAN A., BUCK R. C. STRUCTURE OF THE MITOTIC SPINDLE IN L STRAIN FIBROBLASTS. J Cell Biol. 1965 Mar;24:433–444. doi: 10.1083/jcb.24.3.433. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Murray R. G., Murray A. S., Pizzo A. The fine structure of mitosis in rat thymic lymphocytes. J Cell Biol. 1965 Aug;26(2):601–619. doi: 10.1083/jcb.26.2.601. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Phillips D. M. Fine structure of Sciara coprophila sperm. J Cell Biol. 1966 Sep;30(3):499–517. doi: 10.1083/jcb.30.3.499. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Phillips D. M. Observations on spermiogenesis in the fungus gnat Sciara coprophila. J Cell Biol. 1966 Sep;30(3):477–497. doi: 10.1083/jcb.30.3.477. [DOI] [PMC free article] [PubMed] [Google Scholar]
- RENAUD F. L., SWIFT H. THE DEVELOPMENT OF BASAL BODIES AND FLAGELLA IN ALLOMYCES ARBUSCULUS. J Cell Biol. 1964 Nov;23:339–354. doi: 10.1083/jcb.23.2.339. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Randall J., Disbrey C. Evidence for the presence of DNA at basal body sites in Tetrahymena pyriformis. Proc R Soc Lond B Biol Sci. 1965 Jul 27;162(989):473–491. doi: 10.1098/rspb.1965.0051. [DOI] [PubMed] [Google Scholar]
- Robinow C. F., Marak J. A fiber apparatus in the nucleus of the yeast cell. J Cell Biol. 1966 Apr;29(1):129–151. doi: 10.1083/jcb.29.1.129. [DOI] [PMC free article] [PubMed] [Google Scholar]
- VENABLE J. H., COGGESHALL R. A SIMPLIFIED LEAD CITRATE STAIN FOR USE IN ELECTRON MICROSCOPY. J Cell Biol. 1965 May;25:407–408. doi: 10.1083/jcb.25.2.407. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Werner G. Periodisch quergestreifte Filamente ünd ihre Veränderungen während der Spermatogenese bei Bombina variegata L. Z Zellforsch Mikrosk Anat. 1966;71(2):245–255. [PubMed] [Google Scholar]
