Abstract
Though the dictyosome of the Golgi apparatus appears to be generally distributed in plant and animal cells, it is here described for the first time in the fungi. The present report illustrates, in electron micrographs of thin sections, the characteristic structure of the Golgi dictyosome in a special cell type of a supporting pseudo-tissue (the inner ectal excipulum) of a highly evolved Ascomycete, Neobulgaria pura (Fr.) Petrak, a monotypic discomycete. This organelle may secrete the gelatinous matrix filling the cup formed by the inner ectal excipulum. All the other cells in this species appear more typical of fungal cells; i.e., they have no dictyosome and, unlike the cup-forming cells, they show characteristic continuities of the plasma membrane with the perinuclear cisternae. The dictyosome, in those cells in which it appears in this fungus, is formed by a series of vesiculations of the outer component of the nuclear envelope that align to form a stack of sacs. The sacs near the nucleus are flattened (by what appears to be an intermembrane cement) while those near the plasma membrane are more distended. These observations suggest three possibilities: first, fungi may be more closely related to other eukaryotic cells than previously suspected from electron microscopic studies; second, the outer nuclear membrane may have been the primitive precursor of the dictyosome; and third, the inverse relationship of the occurrence of the nuclear membrane plasma membrane continuities and the dictyosome suggests that the latter may have evolved as a means of removing from the cell the products of reactions occurring on a discontinuous membrane system.
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- BLONDEL B., TURIAN G. Relation between basophilia and fine structure of cytoplasm in the fungus Allomyces macrogynus Em. J Biophys Biochem Cytol. 1960 Feb;7:127–134. doi: 10.1083/jcb.7.1.127. [DOI] [PMC free article] [PubMed] [Google Scholar]
- CONTI S. F., NAYLOR H. B. Electron microscopy of ultrathin sections of Schizosaccharomyces octosporus. II. Morphological and cytological changes preceding ascospore formation. J Bacteriol. 1960 Mar;79:331–340. doi: 10.1128/jb.79.3.331-340.1960. [DOI] [PMC free article] [PubMed] [Google Scholar]
- CONTI S. F., NAYLOR H. B. Study of life-cycle of Schizosaccharomyces octosporus by means of ultra-thin sectioning and electron microscopy. Nature. 1960 Feb 27;185:633–634. doi: 10.1038/185633a0. [DOI] [PubMed] [Google Scholar]
- HASHIMOTO T., CONTI S. F., NAYLOR H. B. Nuclear changes occurring during bud-formation in Saccharomyces cerevisiae as revealed by ultra-thin sectioning. Nature. 1958 Aug 16;182(4633):454–454. doi: 10.1038/182454a0. [DOI] [PubMed] [Google Scholar]
- HASHIMOTO T., CONTI S. F., NAYLOR H. B. Studies of the fine structure of microorganisms. IV. Observations on budding Saccharomyces cerevisiae by light and electron microscopy. J Bacteriol. 1959 Mar;77(3):344–354. doi: 10.1128/jb.77.3.344-354.1959. [DOI] [PMC free article] [PubMed] [Google Scholar]
- MANTON I. On a reticular derivative from Golgi bodies in the meristem of Anthroceros. J Biophys Biochem Cytol. 1960 Sep;8:221–231. doi: 10.1083/jcb.8.1.221. [DOI] [PMC free article] [PubMed] [Google Scholar]
- MOLLENHAUER H. H., WHALEY W. G., LEECH J. H. A function of the Golgi apparatus in outer rootcap cells. J Ultrastruct Res. 1961 Apr;5:193–200. doi: 10.1016/s0022-5320(61)90014-4. [DOI] [PubMed] [Google Scholar]
- MOORE R. T., McALEAR J. H. Fine structure of mycota. Reconstruction from skipped serial sections of the nuclear envelope and its continuity with the plasma membrane. Exp Cell Res. 1961 Sep;24:588–592. doi: 10.1016/0014-4827(61)90460-8. [DOI] [PubMed] [Google Scholar]
- MOORE R. T., McALEAR J. H. Observations on ascospore initiation in the discomycete Dasyscyphus sp. J Gen Microbiol. 1962 Jun;28:211–213. doi: 10.1099/00221287-28-2-211. [DOI] [PubMed] [Google Scholar]
- McALEAR J. H., EDWARDS G. A. [Continuity of plasma membrane and nuclear membrane]. Exp Cell Res. 1959 Mar;16(3):689–692. doi: 10.1016/0014-4827(59)90139-9. [DOI] [PubMed] [Google Scholar]
- PALADE G. E., SIEKEVITZ P. Pancreatic microsomes; an integrated morphological and biochemical study. J Biophys Biochem Cytol. 1956 Nov 25;2(6):671–690. doi: 10.1083/jcb.2.6.671. [DOI] [PMC free article] [PubMed] [Google Scholar]
- PORTER K. R., MACHADO R. D. Studies on the endoplasmic reticulum. IV. Its form and distribution during mitosis in cells of onion root tip. J Biophys Biochem Cytol. 1960 Feb;7:167–180. doi: 10.1083/jcb.7.1.167. [DOI] [PMC free article] [PubMed] [Google Scholar]
- ROBINOW C. F. The structure and behavior of the nuclei in spores and growing hyphae of Mucorales. I. Mucor hiemalis and Mucor fragilis. Can J Microbiol. 1957 Aug;3(5):771–789. doi: 10.1139/m57-087. [DOI] [PubMed] [Google Scholar]
- SIEKEVITZ P., PALADE G. E. A cytochemical study on the pancreas of the guinea pig. I. Isolation and enzymatic activities of cell fractions. J Biophys Biochem Cytol. 1958 Mar 25;4(2):203–218. doi: 10.1083/jcb.4.2.203. [DOI] [PMC free article] [PubMed] [Google Scholar]
- SIEKEVITZ P., PALADE G. E. A cytochemical study on the pancreas of the guinea pig. II. Functional variations in the enzymatic activity of microsomes. J Biophys Biochem Cytol. 1958 May 25;4(3):309–318. doi: 10.1083/jcb.4.3.309. [DOI] [PMC free article] [PubMed] [Google Scholar]
- SIEKEVITZ P., PALADE G. E. A cytochemical study on the pancreas of the guinea pig. IV. Chemical and metabolic investigation of the ribonucleoprotein particles. J Biophys Biochem Cytol. 1959 Jan 25;5(1):1–10. doi: 10.1083/jcb.5.1.1. [DOI] [PMC free article] [PubMed] [Google Scholar]
- THYAGARAJAN T. R., CONTI S. F., NAYLOR H. B. Electron microscopy of Rhodotorula glutinis. J Bacteriol. 1962 Feb;83:381–394. doi: 10.1128/jb.83.2.381-394.1962. [DOI] [PMC free article] [PubMed] [Google Scholar]
