Literature DB >> 14329469

ELECTRON MICROSCOPY OF CELL FUSION IN CONJUGATING HANSENULA WINGEI.

S F CONTI, T D BROCK.   

Abstract

Conti, S. F. (Dartmouth Medical School, Hanover, N.H.), and T. D. Brock. Electron microscopy of cell fusion in conjugating Hansenula wingei. J. Bacteriol. 90:524-533. 1965.-The heterothallic yeast Hansenula wingei is a favorable organism for the study of the process of cell fusion, since strong agglutination of cells of the two mating types ensures a high percentage of cell fusions. The initial agglutination reaction results in cell-wall deformation, so that the walls in the region of contact are tightly appressed over an extensive area. The fusion process is initiated when the walls of two cells elongate, and this elongation seems to be restricted to the region where the cells touch. Occasionally, one cell is seen to push in the wall of the other, but in many cases both cells elongate equally, as would be expected in an isogamous organism. The precise disposition of the elongating wall probably reflects the manner in which the cells initially become associated in the agglutinated cell clump. Soon after wall elongation begins, cell-wall fusion occurs along the margin of contact. Only after fusion is complete is the wall separating the two cells dissolved away. If wall dissolution begins at one edge of the conjugation tube, a flap is formed in which can be seen the remnants of the fused walls. Alternatively, dissolution can begin at the center of the conjugation tube, proceeding towards the outside. Conjugating cells are uninucleate, and the nuclei are large and frequently lobed or elongated. After the conjugation tube is formed, the nuclei migrate towards the center, and fusion occurs only over a small region where the nuclear membranes come in contact. After nuclear fusion, the first diploid bud forms from the conjugation tube and at right angles to the tube axis. The diploid nucleus then migrates into this bud. Frequently, in the later stages of conjugation, a large vacuole develops in each of the original cells. All of the above events will occur in a medium devoid of a nitrogen source and in which vegetative budding will not occur.

Entities:  

Keywords:  CELL NUCLEUS; CELL STRUCTURE; CULTURE MEDIA; CYTOLOGY; EXPERIMENTAL LAB STUDY; METABOLISM; MICROSCOPY, ELECTRON; YEASTS

Mesh:

Substances:

Year:  1965        PMID: 14329469      PMCID: PMC315674          DOI: 10.1128/jb.90.2.524-533.1965

Source DB:  PubMed          Journal:  J Bacteriol        ISSN: 0021-9193            Impact factor:   3.490


  7 in total

1.  Electron microscopy of Rhodotorula glutinis.

Authors:  T R THYAGARAJAN; S F CONTI; H B NAYLOR
Journal:  J Bacteriol       Date:  1962-02       Impact factor: 3.490

2.  Physiology of the conjugation process in the yeast Hansenula wingei.

Authors:  T D BROCK
Journal:  J Gen Microbiol       Date:  1961-11

3.  Electron microscopy of ultrathin sections of Schizosaccharomyces octosporus. II. Morphological and cytological changes preceding ascospore formation.

Authors:  S F CONTI; H B NAYLOR
Journal:  J Bacteriol       Date:  1960-03       Impact factor: 3.490

4.  Mating reaction in the yeast Hansenula wingei; preliminary observations and quantitation.

Authors:  T D BROCK
Journal:  J Bacteriol       Date:  1958-06       Impact factor: 3.490

5.  Isolation of beta-dihydroequilin and alpha-dihydroequilenin from the urine of pregnant mares.

Authors:  W L GLEN; R BARBER; H M MCCONKEY; G A GRANT
Journal:  Nature       Date:  1956-04-21       Impact factor: 49.962

6.  Improvements in epoxy resin embedding methods.

Authors:  J H LUFT
Journal:  J Biophys Biochem Cytol       Date:  1961-02

7.  Studies on the fine structure of microorganisms. V. Morphogenesis of nuclear and membrane structures during ascospore formation in yeast.

Authors:  T HASHIMOTO; P GERHARDT; S F CONTI; H B NAYLOR
Journal:  J Biophys Biochem Cytol       Date:  1960-04
  7 in total
  13 in total

1.  Behavior of spindles and spindle plaques in the cell cycle and conjugation of Saccharomyces cerevisiae.

Authors:  B Byers; L Goetsch
Journal:  J Bacteriol       Date:  1975-10       Impact factor: 3.490

2.  Morphogenic effects of alpha-factor on Saccharomyces cerevisiae a cells.

Authors:  P N Lipke; A Taylor; C E Ballou
Journal:  J Bacteriol       Date:  1976-07       Impact factor: 3.490

3.  Mating reaction in Saccharomyces cerevisiae. 3. Changes in autolytic activity.

Authors:  C Shimoda; N Yanagishima
Journal:  Arch Mikrobiol       Date:  1972

Review 4.  Molecular basis of mating in the yeast hansenula wingei.

Authors:  M A Crandall; T D Brock
Journal:  Bacteriol Rev       Date:  1968-09

5.  Surface structure of yeast protoplasts.

Authors:  E Streiblová
Journal:  J Bacteriol       Date:  1968-02       Impact factor: 3.490

6.  Mating responses in the yeast Hansenula holstii.

Authors:  A I Herman
Journal:  Antonie Van Leeuwenhoek       Date:  1971       Impact factor: 2.271

7.  Biochemical and cellular changes occuring during conjugation in Hansenula wingei.

Authors:  T D Brock
Journal:  J Bacteriol       Date:  1965-10       Impact factor: 3.490

8.  Cytoplasmic inheritance in Saccharomyces cerevisiae: comparison of zygotic mitochondrial inheritance patterns.

Authors:  K J Aufderheide; R G Johnson
Journal:  Mol Gen Genet       Date:  1976-03-30

9.  Role of enzymes in growth and morphology of Neurospora crassa: cell-wall-bound enzymes and their possible role in branching.

Authors:  P R Mahadevan; U R Mahadkar
Journal:  J Bacteriol       Date:  1970-03       Impact factor: 3.490

10.  Morphogenesis of ascospores in Saccharomyces cerevisiae.

Authors:  E Guth; T Hashimoto; S F Conti
Journal:  J Bacteriol       Date:  1972-02       Impact factor: 3.490

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