Dynamic localization of the Swe1 regulator Hsl7 during the Saccharomyces cerevisiae cell cycle

被引:69
作者
Cid, VJ
Shulewitz, MJ
McDonald, KL
Thorner, J [1 ]
机构
[1] Univ Calif Berkeley, Dept Mol & Cell Biol, Div Biochem & Mol Biol, Berkeley, CA 94720 USA
[2] Univ Calif Berkeley, Electron Microscopy Lab, Berkeley, CA 94720 USA
关键词
D O I
10.1091/mbc.12.6.1645
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
In Saccharomyces cerevisiae, entry into mitosis requires activation of the cyclin-dependent kinase Cdc28 in its cyclin B (Clb)-associated form. Clb-bound Cdc28 is susceptible to inhibitory tyrosine phosphorylation by Swe1 protein kinase. Swe1 is itself negatively regulated by Hsl1, a Nim1-related protein kinase, and by Hsl7, a presumptive protein-arginine methyltransferase. In vivo all three proteins localize to the bud neck in a septin-dependent manner, consistent with our previous proposal that formation of Hsl1-Hsl7-Swe1 complexes constitutes a checkpoint that monitors septin assembly. We show here that Hsl7 is phosphorylated by Hsl1 in immune-complex kinase assays and can physically associate in vitro with either Hsl1 or Swe1 in the absence of any other yeast proteins. With the use of both the two-hybrid method and in vitro binding assays, we found that Hsl7 contains distinct binding sites for Hsl1 and Swe1. A differential interaction trap approach was used to isolate four single-site substitution mutations in Hsl7, which cluster within a discrete region of its N-terminal domain, that are specifically defective in binding Hsl1. When expressed in hsl7 Delta cells, each of these Hsl7 point mutants is unable to localize at the bud neck and cannot mediate down-regulation of Swe1, but retains other functions of Hsl7, including oligomerization and association with Swe1. GFP-fusions of these Hsl1-binding defective Hsl7 proteins localize as a bright perinuclear dot, but never localize to the bud neck; likewise, in hsl1 Delta cells, a GFP-fusion to wild-type Hsl7 or native Hsl7 localizes to this dot. Cell synchronization studies showed that, normally, Hsl7 localizes to the dot, but only in cells in the GI phase of the cell cycle. Immunofluorescence analysis and immunoelectron microscopy established that the dot corresponds to the outer plaque of the spindle pole body (SPB). These data demonstrate that association between Hsl1 and Hsl7 at the bud neck is required to alleviate Swe1-imposed G2-M delay. Hsl7 localization at the SPB during G1 may play some additional role in fine-tuning the coordination between nuclear and cortical events before mitosis.
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页码:1645 / 1669
页数:25
相关论文
共 96 条
[1]   The spindle checkpoint [J].
Amon, A .
CURRENT OPINION IN GENETICS & DEVELOPMENT, 1999, 9 (01) :69-75
[2]   CLOSING THE CELL-CYCLE CIRCLE IN YEAST - G2 CYCLIN PROTEOLYSIS INITIATED AT MITOSIS PERSISTS UNTIL THE ACTIVATION OF G1 CYCLINS IN THE NEXT CYCLE [J].
AMON, A ;
IRNIGER, S ;
NASMYTH, K .
CELL, 1994, 77 (07) :1037-1050
[3]   High rates of actin filament turnover in budding yeast and roles for actin in establishment and maintenance of cell polarity revealed using the actin inhibitor latrunculin-A [J].
Ayscough, KR ;
Stryker, J ;
Pokala, N ;
Sanders, M ;
Crews, P ;
Drubin, DG .
JOURNAL OF CELL BIOLOGY, 1997, 137 (02) :399-416
[4]  
Balasubramanian MK, 2000, J CELL SCI, V113, P1503
[5]   A mechanism for coupling exit from mitosis to partitioning of the nucleus [J].
Bardin, AJ ;
Visintin, R ;
Amon, A .
CELL, 2000, 102 (01) :21-31
[6]   Differential regulation of transcription: Repression by unactivated mitogen-activated protein kinase Kss1 requires the Dig1 and Dig2 proteins [J].
Bardwell, L ;
Cook, JG ;
Zhu-Shimoni, JX ;
Voora, D ;
Thorner, J .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (26) :15400-15405
[7]  
Bardwell L, 1996, MOL CELL BIOL, V16, P3637
[8]   Nim1-related kinases coordinate cell cycle progression with the organization of the peripheral cytoskeleton in yeast [J].
Barral, Y ;
Parra, M ;
Bidlingmaier, S ;
Snyder, M .
GENES & DEVELOPMENT, 1999, 13 (02) :176-187
[9]   Compartmentalization of the cell cortex by septins is required for maintenance of cell polarity in yeast [J].
Barral, Y ;
Mermall, V ;
Mooseker, MS ;
Snyder, M .
MOLECULAR CELL, 2000, 5 (05) :841-851
[10]   DIRECT INTERACTION BETWEEN YEAST SPINDLE POLE BODY COMPONENTS - KAR1P IS REQUIRED FOR CDC31P LOCALIZATION TO THE SPINDLE POLE BODY [J].
BIGGINS, S ;
ROSE, MD .
JOURNAL OF CELL BIOLOGY, 1994, 125 (04) :843-852