Literature DB >> 7730410

Role of Bud3p in producing the axial budding pattern of yeast.

J Chant1, M Mischke, E Mitchell, I Herskowitz, J R Pringle.   

Abstract

Yeast cells can select bud sites in either of two distinct spatial patterns. a cells and alpha cells typically bud in an axial pattern, in which both mother and daughter cells form new buds adjacent to the preceding division site. In contrast, a/alpha cells typically bud in a bipolar pattern, in which new buds can form at either pole of the cell. The BUD3 gene is specifically required for the axial pattern of budding: mutations of BUD3 (including a deletion) affect the axial pattern but not the bipolar pattern. The sequence of BUD3 predicts a product (Bud3p) of 1635 amino acids with no strong or instructive similarities to previously known proteins. However, immunofluorescence localization of Bud3p has revealed that it assembles in an apparent double ring encircling the mother-bud neck shortly after the mitotic spindle forms. The Bud3p structure at the neck persists until cytokinesis, when it splits to yield a single ring of Bud3p marking the division site on each of the two progeny cells. These single rings remain for much of the ensuing unbudded phase and then disassemble. The Bud3p rings are indistinguishable from those of the neck filament-associated proteins (Cdc3p, Cdc10p, Cdc11p, and Cdc12p), except that the latter proteins assemble before bud emergence and remain in place for the duration of the cell cycle. Upon shift of a temperature-sensitive cdc12 mutant to restrictive temperature, localization of both Bud3p and the neck filament-associated proteins is rapidly lost. In addition, a haploid cdc11 mutant loses its axial-budding pattern upon shift to restrictive temperature. Taken together, the data suggest that Bud3p and the neck filaments are linked in a cycle in which each controls the position of the other's assembly: Bud3p assembles onto the neck filaments in one cell cycle to mark the site for axial budding (including assembly of the new ring of neck filaments) in the next cell cycle. As the expression and localization of Bud3p are similar in a, alpha, and a/alpha cells, additional regulation must exist such that Bud3p restricts the position of bud formation in a and alpha cells but not in a/alpha cells.

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Year:  1995        PMID: 7730410      PMCID: PMC2120433          DOI: 10.1083/jcb.129.3.767

Source DB:  PubMed          Journal:  J Cell Biol        ISSN: 0021-9525            Impact factor:   10.539


  52 in total

Review 1.  The role of p34 kinases in the G1 to S-phase transition.

Authors:  S I Reed
Journal:  Annu Rev Cell Biol       Date:  1992

2.  Functional cloning of BUD5, a CDC25-related gene from S. cerevisiae that can suppress a dominant-negative RAS2 mutant.

Authors:  S Powers; E Gonzales; T Christensen; J Cubert; D Broek
Journal:  Cell       Date:  1991-06-28       Impact factor: 41.582

3.  The complete DNA sequence of yeast chromosome III.

Authors:  S G Oliver; Q J van der Aart; M L Agostoni-Carbone; M Aigle; L Alberghina; D Alexandraki; G Antoine; R Anwar; J P Ballesta; P Benit
Journal:  Nature       Date:  1992-05-07       Impact factor: 49.962

4.  Transient G1 arrest of S. cerevisiae cells of mating type alpha by a factor produced by cells of mating type a.

Authors:  L E Wilkinson; J R Pringle
Journal:  Exp Cell Res       Date:  1974-11       Impact factor: 3.905

Review 5.  Budding and cell polarity in Saccharomyces cerevisiae.

Authors:  J Chant; J R Pringle
Journal:  Curr Opin Genet Dev       Date:  1991-10       Impact factor: 5.578

6.  Cellular morphogenesis in the Saccharomyces cerevisiae cell cycle: localization of the CDC11 gene product and the timing of events at the budding site.

Authors:  S K Ford; J R Pringle
Journal:  Dev Genet       Date:  1991

7.  Specification of sites for polarized growth in Saccharomyces cerevisiae and the influence of external factors on site selection.

Authors:  K Madden; M Snyder
Journal:  Mol Biol Cell       Date:  1992-09       Impact factor: 4.138

8.  RSR1, a ras-like gene homologous to Krev-1 (smg21A/rap1A): role in the development of cell polarity and interactions with the Ras pathway in Saccharomyces cerevisiae.

Authors:  R Ruggieri; A Bender; Y Matsui; S Powers; Y Takai; J R Pringle; K Matsumoto
Journal:  Mol Cell Biol       Date:  1992-02       Impact factor: 4.272

9.  A highly ordered ring of membrane-associated filaments in budding yeast.

Authors:  B Byers; L Goetsch
Journal:  J Cell Biol       Date:  1976-06       Impact factor: 10.539

10.  Studies concerning the temporal and genetic control of cell polarity in Saccharomyces cerevisiae.

Authors:  M Snyder; S Gehrung; B D Page
Journal:  J Cell Biol       Date:  1991-08       Impact factor: 10.539

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  91 in total

1.  Genetic analysis of default mating behavior in Saccharomyces cerevisiae.

Authors:  R Dorer; C Boone; T Kimbrough; J Kim; L H Hartwell
Journal:  Genetics       Date:  1997-05       Impact factor: 4.562

2.  Identification and characterization of genes required for hyphal morphogenesis in the filamentous fungus Aspergillus nidulans.

Authors:  S D Harris; A F Hofmann; H W Tedford; M P Lee
Journal:  Genetics       Date:  1999-03       Impact factor: 4.562

3.  Genetic analysis of the bipolar pattern of bud site selection in the yeast Saccharomyces cerevisiae.

Authors:  J E Zahner; H A Harkins; J R Pringle
Journal:  Mol Cell Biol       Date:  1996-04       Impact factor: 4.272

4.  The LIM domain-containing Dbm1 GTPase-activating protein is required for normal cellular morphogenesis in Saccharomyces cerevisiae.

Authors:  G C Chen; L Zheng; C S Chan
Journal:  Mol Cell Biol       Date:  1996-04       Impact factor: 4.272

5.  Functional analysis of the interaction between Afr1p and the Cdc12p septin, two proteins involved in pheromone-induced morphogenesis.

Authors:  L Giot; J B Konopka
Journal:  Mol Biol Cell       Date:  1997-06       Impact factor: 4.138

6.  Aspergillus nidulans septin AspB plays pre- and postmitotic roles in septum, branch, and conidiophore development.

Authors:  Patrick J Westfall; Michelle Momany
Journal:  Mol Biol Cell       Date:  2002-01       Impact factor: 4.138

7.  Regulation of septum formation by the Bud3-Rho4 GTPase module in Aspergillus nidulans.

Authors:  Haoyu Si; Daniela Justa-Schuch; Stephan Seiler; Steven D Harris
Journal:  Genetics       Date:  2010-02-22       Impact factor: 4.562

8.  Regulation of Cdc42 polarization by the Rsr1 GTPase and Rga1, a Cdc42 GTPase-activating protein, in budding yeast.

Authors:  Mid Eum Lee; Wing-Cheong Lo; Kristi E Miller; Ching-Shan Chou; Hay-Oak Park
Journal:  J Cell Sci       Date:  2015-04-23       Impact factor: 5.285

9.  The role of Cdc42p GTPase-activating proteins in assembly of the septin ring in yeast.

Authors:  Juliane P Caviston; Mark Longtine; John R Pringle; Erfei Bi
Journal:  Mol Biol Cell       Date:  2003-07-25       Impact factor: 4.138

10.  The roles of bud-site-selection proteins during haploid invasive growth in yeast.

Authors:  Paul J Cullen; George F Sprague
Journal:  Mol Biol Cell       Date:  2002-09       Impact factor: 4.138

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