Msb1 Interacts with Cdc42, Boi1, and Boi2 and May Coordinate Cdc42 and Rho1 Functions during Early Stage of Bud Development in Budding Yeast

被引:7
|
作者
Liao, Yuan [1 ]
He, Fei [1 ]
Gong, Ting [1 ]
Bi, Erfei [2 ]
Gao, Xiang-Dong [1 ]
机构
[1] Wuhan Univ, State Key Lab Virol, Coll Life Sci, Wuhan 430072, Peoples R China
[2] Univ Penn, Dept Cell & Dev Biol, Perelman Sch Med, Philadelphia, PA 19104 USA
来源
PLOS ONE | 2013年 / 8卷 / 06期
基金
中国国家自然科学基金; 美国国家卫生研究院;
关键词
SACCHAROMYCES-CEREVISIAE; CELL POLARITY; SMALL GTPASES; PROTEIN; IDENTIFICATION; GROWTH; GENES; POLARIZATION; ROLES; CYTOKINESIS;
D O I
10.1371/journal.pone.0066321
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Msb1 is not essential for growth in the budding yeast Saccharomyces cerevisiae since msb1 Delta cells do not display obvious phenotypes. Genetic studies suggest that Msb1 positively regulates Cdc42 function during bud development, since high-copy MSB1 suppressed the growth defect of temperature-sensitive cdc24 and cdc42 mutants at restrictive temperature, while deletion of MSB1 showed synthetic lethality with cdc24, bem1, and bem2 mutations. However, the mechanism of how Msb1 regulates Cdc42 function remains poorly understood. Here, we show that Msb1 localizes to sites of polarized growth during bud development and interacts with Cdc42 in the cells. In addition, Msb1 interacts with Boi1 and Boi2, two scaffold proteins that also interact with Cdc42 and Bem1. These findings suggest that Msb1 may positively regulate Cdc42 function by interacting with Cdc42, Boi1, and Boi2, which may promote the efficient assembly of Cdc42, Cdc24, and other proteins into a functional complex. We also show that Msb1 interacts with Rho1 in the cells and Msb1 overproduction inhibits the growth of rho1-104 and rho1-3 but not rho1-2 cells. The growth inhibition appears to result from the down-regulation of Rho1 function in glucan synthesis, specifically during early stage of bud development. These results suggest that Msb1 may coordinate Cdc42 and Rho1 functions during early stage of bud development by promoting Cdc42 function and inhibiting Rho1 function. Msb1 overproduction also affects cell morphology, septin organization, and causes increased, aberrant deposition of 1,3-beta-glucan and chitin at the mother-bud neck. However, the stimulation of glucan synthesis mainly occurs during late, but not early, stage of bud development.
引用
收藏
页数:11
相关论文
共 37 条
  • [31] REGULATION OF AMINO ACID TRANSPORTER TRAFFICKING BY MTORC2 IN PRIMARY HUMAN TROPHOBLAST CELLS IS MEDIATED BY THE RHO FAMILY OF GTP PROTEINS CDC42 AND RAC1
    Rosario, Fredrick J.
    Powell, Theresa
    Jansson, Thomas
    PLACENTA, 2017, 57 : 251 - 252
  • [32] Golgi-localized GAP for Cdc42 functions downstream of ARF1 to control Arp2/3 complex and F-actin dynamics
    Thierry Dubois
    Olivia Paléotti
    Alexander A. Mironov
    Vincent Fraisier
    Theresia E. B. Stradal
    Maria Antonietta De Matteis
    Michel Franco
    Philippe Chavrier
    Nature Cell Biology, 2005, 7 : 353 - 364
  • [33] Golgi-localized GAP for Cdc42 functions downstream of ARF1 to control Arp2/3 complex and F-actin dynamics
    Dubois, T
    Paléotti, O
    Mironov, AA
    Fraisier, V
    Stradal, TEB
    De Matteis, MA
    Franco, M
    Chavrier, P
    NATURE CELL BIOLOGY, 2005, 7 (04) : 353 - U9
  • [34] Vav2 lacks Ca2+ entry-promoting scaffolding functions unique to Vav1 and inhibits T cell activation via Cdc42
    Fray, Michael A.
    Charpentier, John C.
    Sylvain, Nicholas R.
    Seminario, Maria-Cristina
    Bunnell, Stephen C.
    JOURNAL OF CELL SCIENCE, 2020, 133 (05)
  • [35] RETRACTED: YRKL sequence of influenza virus M1 functions as the L domain motif and interacts with VPS28 and Cdc42 (Retracted article. See vol 80 pg 10289 2006)
    Hui, EKW
    Barman, S
    Tang, DHP
    France, B
    Nayak, DP
    JOURNAL OF VIROLOGY, 2006, 80 (05) : 2291 - 2308
  • [36] Selective control of membrane ruffling and actin plaque assembly by the Rho GTPases Rac1 and CDC42 in Fc epsilon RI-activated rat basophilic leukemia (RBL-2H3) cells
    Guillemot, JC
    Montcourrier, P
    Vivier, E
    Davoust, J
    Chavrier, P
    JOURNAL OF CELL SCIENCE, 1997, 110 : 2215 - 2225
  • [37] Differential signalling by muscarinic receptors in smooth muscle:: m2-mediated inactivation of myosin light chain kinase via Gi3, Cdc42/Rac1 and p21-activated kinase 1 pathway, and m3-mediated MLC20 (20 kDa regulatory light chain of myosin II) phosphorylation via Rho-associated kinase/myosin phosphatase targeting subunit 1 and protein kinase C/CPI-17 pathway
    Murthy, KS
    Zhou, HP
    Grider, JR
    Brautigan, DL
    Eto, M
    Makhlouf, GM
    BIOCHEMICAL JOURNAL, 2003, 374 : 145 - 155