Aip3p/Bud6p, a yeast actin-interacting protein that is involved in morphogenesis and the selection of bipolar budding sites

被引:150
作者
Amberg, DC
Zahner, JE
Mulholland, JW
Pringle, JR
Botstein, D
机构
[1] STANFORD UNIV, SCH MED, DEPT GENET, STANFORD, CA 94305 USA
[2] UNIV N CAROLINA, DEPT BIOL, CHAPEL HILL, NC 27599 USA
关键词
D O I
10.1091/mbc.8.4.729
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
A search for Saccharomyces cerevisiae proteins that interact with actin in the two-hybrid system and a screen for mutants that affect the bipolar budding pattern identified the same gene, AIP3/BUD6. This gene is not essential for mitotic growth but is necessary for normal morphogenesis. MATa/alpha daughter cells lacking Aip3p place their first buds normally at their distal poles but choose random sites for budding in subsequent cell cycles. This suggests that actin and associated proteins are involved in placing the bipolar positional marker at the division site but not at the distal tip of the daughter cell. In addition, although aip3 mutant cells are not obviously defective in the initial polarization of the cytoskeleton at the time of bud emergence, they appear to lose cytoskeletal polarity as the bud enlarges, resulting in the formation of cells that are larger and rounder than normal. aip3 mutant cells also show inefficient nuclear migration and nuclear division, defects in the organization of the secretory system, and abnormal septation, all defects that presumably reflect the involvement of Aip3p in the organization and/or function of the actin cytoskeleton. The sequence of Aip3p is novel but contains a predicted coiled-coil domain near its C terminus that may mediate the observed homo-oligomerization of the protein. Aip3p shows a distinctive localization pattern that correlates well with its likely sites of action: it appears at the presumptive bud site prior to bud emergence, remains near the tips of small buds, and forms a ring (or pair of rings) in the mother-bud neck that is detectable early in the cell cycle but becomes more prominent prior to cytokinesis. Surprisingly, the localization of Aip3p does not appear to require either polarized actin or the septin proteins of the neck filaments.
引用
收藏
页码:729 / 753
页数:25
相关论文
共 89 条
  • [1] REQUIREMENT OF YEAST FIMBRIN FOR ACTIN ORGANIZATION AND MORPHOGENESIS INVIVO
    ADAMS, AEM
    BOTSTEIN, D
    DRUBIN, DG
    [J]. NATURE, 1991, 354 (6352) : 404 - 408
  • [2] RELATIONSHIP OF ACTIN AND TUBULIN DISTRIBUTION TO BUD GROWTH IN WILD-TYPE AND MORPHOGENETIC-MUTANT SACCHAROMYCES-CEREVISIAE
    ADAMS, AEM
    PRINGLE, JR
    [J]. JOURNAL OF CELL BIOLOGY, 1984, 98 (03) : 934 - 945
  • [3] ALTSCHUL SF, 1990, J MOL BIOL, V215, P403, DOI 10.1006/jmbi.1990.9999
  • [4] PURIFICATION, CHARACTERIZATION, AND IMMUNOFLUORESCENCE LOCALIZATION OF SACCHAROMYCES-CEREVISIAE CAPPING PROTEIN
    AMATRUDA, JF
    COOPER, JA
    [J]. JOURNAL OF CELL BIOLOGY, 1992, 117 (05) : 1067 - 1076
  • [5] DEFINING PROTEIN INTERACTIONS WITH YEAST ACTIN IN-VIVO
    AMBERG, DC
    BASART, E
    BOTSTEIN, D
    [J]. NATURE STRUCTURAL BIOLOGY, 1995, 2 (01): : 28 - 35
  • [6] PRECISE GENE DISRUPTION IN SACCHAROMYCES-CEREVISIAE BY DOUBLE FUSION POLYMERASE CHAIN-REACTION
    AMBERG, DC
    BOTSTEIN, D
    BEASLEY, EM
    [J]. YEAST, 1995, 11 (13) : 1275 - 1280
  • [7] [Anonymous], 1988, Antibodies: A Laboratory Manual
  • [8] Ausubel FA, 1995, CURRENT PROTOCOLS MO
  • [9] AYSCOUGH KR, 1997, IN PRESS J CELL BIOL
  • [10] A SIMPLE AND EFFICIENT METHOD FOR DIRECT GENE DELETION IN SACCHAROMYCES-CEREVISIAE
    BAUDIN, A
    OZIERKALOGEROPOULOS, O
    DENOUEL, A
    LACROUTE, F
    CULLIN, C
    [J]. NUCLEIC ACIDS RESEARCH, 1993, 21 (14) : 3329 - 3330