Literature DB >> 7841518

Symmetric cell division in pseudohyphae of the yeast Saccharomyces cerevisiae.

S J Kron1, C A Styles, G R Fink.   

Abstract

Laboratory strains of Saccharomyces cerevisiae are dimorphic; in response to nitrogen starvation they switch from a yeast form (YF) to a filamentous pseudohyphal (PH) form. Time-lapse video microscopy of dividing cells reveals that YF and PH cells differ in their cell cycles and budding polarity. The YF cell cycle is controlled at the G1/S transition by the cell-size checkpoint Start. YF cells divide asymmetrically, producing small daughters from full-sized mothers. As a result, mothers and daughters bud asynchronously. Mothers bud immediately but daughters grow in G1 until they achieve a critical cell size. By contrast, PH cells divide symmetrically, restricting mitosis until the bud grows to the size of the mother. Thus, mother and daughter bud synchronously in the next cycle, without a G1 delay before Start. YF and PH cells also exhibit distinct bud-site selection patterns. YF cells are bipolar, producing their second and subsequent buds at either pole. PH cells are unipolar, producing their second and subsequent buds only from the end opposite the junction with their mother. We propose that in PH cells a G2 cell-size checkpoint delays mitosis until bud size reaches that of the mother cell. We conclude that yeast and PH forms are distinct cell types each with a unique cell cycle, budding pattern, and cell shape.

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Year:  1994        PMID: 7841518      PMCID: PMC301123          DOI: 10.1091/mbc.5.9.1003

Source DB:  PubMed          Journal:  Mol Biol Cell        ISSN: 1059-1524            Impact factor:   4.138


  51 in total

Review 1.  G1 events and regulation of cell proliferation.

Authors:  A B Pardee
Journal:  Science       Date:  1989-11-03       Impact factor: 47.728

2.  FUS3 encodes a cdc2+/CDC28-related kinase required for the transition from mitosis into conjugation.

Authors:  E A Elion; P L Grisafi; G R Fink
Journal:  Cell       Date:  1990-02-23       Impact factor: 41.582

3.  An essential G1 function for cyclin-like proteins in yeast.

Authors:  H E Richardson; C Wittenberg; F Cross; S I Reed
Journal:  Cell       Date:  1989-12-22       Impact factor: 41.582

Review 4.  Fluorescence microscopy methods for yeast.

Authors:  J R Pringle; R A Preston; A E Adams; T Stearns; D G Drubin; B K Haarer; E W Jones
Journal:  Methods Cell Biol       Date:  1989       Impact factor: 1.441

5.  Transmission electron microscopy and immunocytochemical studies of yeast: analysis of HMG-CoA reductase overproduction by electron microscopy.

Authors:  R Wright; J Rine
Journal:  Methods Cell Biol       Date:  1989       Impact factor: 1.441

6.  A family of cyclin homologs that control the G1 phase in yeast.

Authors:  J A Hadwiger; C Wittenberg; H E Richardson; M de Barros Lopes; S I Reed
Journal:  Proc Natl Acad Sci U S A       Date:  1989-08       Impact factor: 11.205

7.  G1-specific cyclins of S. cerevisiae: cell cycle periodicity, regulation by mating pheromone, and association with the p34CDC28 protein kinase.

Authors:  C Wittenberg; K Sugimoto; S I Reed
Journal:  Cell       Date:  1990-07-27       Impact factor: 41.582

8.  Identification of a gene necessary for cell cycle arrest by a negative growth factor of yeast: FAR1 is an inhibitor of a G1 cyclin, CLN2.

Authors:  F Chang; I Herskowitz
Journal:  Cell       Date:  1990-11-30       Impact factor: 41.582

9.  Tyrosine phosphorylation of the fission yeast cdc2+ protein kinase regulates entry into mitosis.

Authors:  K L Gould; P Nurse
Journal:  Nature       Date:  1989-11-02       Impact factor: 49.962

10.  A system of shuttle vectors and yeast host strains designed for efficient manipulation of DNA in Saccharomyces cerevisiae.

Authors:  R S Sikorski; P Hieter
Journal:  Genetics       Date:  1989-05       Impact factor: 4.562

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  126 in total

1.  F-box protein Grr1 interacts with phosphorylated targets via the cationic surface of its leucine-rich repeat.

Authors:  Y G Hsiung; H C Chang; J L Pellequer; R La Valle; S Lanker; C Wittenberg
Journal:  Mol Cell Biol       Date:  2001-04       Impact factor: 4.272

2.  Mechanisms controlling differential promoter-occupancy by the yeast forkhead proteins Fkh1p and Fkh2p: implications for regulating the cell cycle and differentiation.

Authors:  P C Hollenhorst; G Pietz; C A Fox
Journal:  Genes Dev       Date:  2001-09-15       Impact factor: 11.361

3.  A role for the Swe1 checkpoint kinase during filamentous growth of Saccharomyces cerevisiae.

Authors:  R La Valle; C Wittenberg
Journal:  Genetics       Date:  2001-06       Impact factor: 4.562

4.  Glucose depletion causes haploid invasive growth in yeast.

Authors:  P J Cullen; G F Sprague
Journal:  Proc Natl Acad Sci U S A       Date:  2000-12-05       Impact factor: 11.205

5.  Modular organization of cellular networks.

Authors:  Alexander W Rives; Timothy Galitski
Journal:  Proc Natl Acad Sci U S A       Date:  2003-01-21       Impact factor: 11.205

6.  Characterization of alcohol-induced filamentous growth in Saccharomyces cerevisiae.

Authors:  M C Lorenz; N S Cutler; J Heitman
Journal:  Mol Biol Cell       Date:  2000-01       Impact factor: 4.138

7.  Role of phosphatidylinositol phosphate signaling in the regulation of the filamentous-growth mitogen-activated protein kinase pathway.

Authors:  Hema Adhikari; Paul J Cullen
Journal:  Eukaryot Cell       Date:  2015-02-27

8.  Aspergillus asexual reproduction and sexual reproduction are differentially affected by transcriptional and translational mechanisms regulating stunted gene expression.

Authors:  J Wu; B L Miller
Journal:  Mol Cell Biol       Date:  1997-10       Impact factor: 4.272

9.  Large-scale analysis of yeast filamentous growth by systematic gene disruption and overexpression.

Authors:  Rui Jin; Craig J Dobry; Phillip J McCown; Anuj Kumar
Journal:  Mol Biol Cell       Date:  2007-11-07       Impact factor: 4.138

10.  AKR1 encodes a candidate effector of the G beta gamma complex in the Saccharomyces cerevisiae pheromone response pathway and contributes to control of both cell shape and signal transduction.

Authors:  P M Pryciak; L H Hartwell
Journal:  Mol Cell Biol       Date:  1996-06       Impact factor: 4.272

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