far4, far5, and far6 define three genes required for efficient activation of MAPKs Fus3 and Kss1 and accumulation of glycogen

被引:11
作者
Cherkasova, V [1 ]
Elion, EA [1 ]
机构
[1] Harvard Univ, Sch Med, Dept Biol Chem & Mol Pharmacol, Boston, MA 02115 USA
关键词
MAP kinase; pheromone response; G1; arrest; Saccharomyces cerevisiae;
D O I
10.1007/s002940100217
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
In Saccharomyces cerevisiae, mating pheromones induce G1 arrest through the activation of two MAP kinases. Fus3 and Kss1. Here we report the isolation of three mutants, far4, far5.. and far6, that have the novel phenotype of regulating both the activity of Fus3 and Kss1 and the accumulation of glycogen. Afar4 mutation constitutively activates Fus3 and Kss1. reduces glycogen, and blocks G1 arrest in the presence of alpha factor. In contrast, far5 and far6 mutations increase glycogen and reduce activation of Fus3 and Kss1 by pheromone. far4, far5, and far6 are recessive and not allelic to FAR1, FAR3, or 14 genes known to regulate the pheromone response. Non-allelic non-complementation occurs between far6 and both far4 and far5, suggesting that FAR6 functionally interacts with FAR4 and FAR5. Additional observations suggest that FAR4 has functional overlap with FAR3, which we also find to regulate glycogen accumulation. Our results suggest that the activation of the mating MAPK cascade and subsequent G1 arrest is influenced by a signal transduction pathway that regulates glycogen. In support of this possibility, we find that Fus3 is activated to a greater extent in a "wimp" strain with defective protein kinase A. Finally, BIM1 and BIK1 have been identified as CEN Suppressors of far5, suggesting that the microtubule apparatus may regulate the ability of the pheromone response pathway to promote G1 arrest.
引用
收藏
页码:13 / 26
页数:14
相关论文
共 65 条
  • [1] [Anonymous], METHOD ENZYMOL
  • [2] Repression of yeast Ste12 transcription factor by direct binding of unphosphorylated Kss1 MAPK and its regulation by the Ste7 MEK
    Bardwell, L
    Cook, JG
    Voora, D
    Baggott, DM
    Martinez, AR
    Thorner, J
    [J]. GENES & DEVELOPMENT, 1998, 12 (18) : 2887 - 2898
  • [3] BIK1, A PROTEIN REQUIRED FOR MICROTUBULE FUNCTION DURING MATING AND MITOSIS IN SACCHAROMYCES-CEREVISIAE, COLOCALIZES WITH TUBULIN
    BERLIN, V
    STYLES, CA
    FINK, GR
    [J]. JOURNAL OF CELL BIOLOGY, 1990, 111 (06) : 2573 - 2586
  • [4] CAMP-INDEPENDENT CONTROL OF SPORULATION, GLYCOGEN-METABOLISM, AND HEAT-SHOCK RESISTANCE IN S-CEREVISIAE
    CAMERON, S
    LEVIN, L
    ZOLLER, M
    WIGLER, M
    [J]. CELL, 1988, 53 (04) : 555 - 566
  • [5] 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
    CHANG, F
    HERSKOWITZ, I
    [J]. CELL, 1990, 63 (05) : 999 - 1011
  • [6] Cherkasova V, 1999, GENETICS, V151, P989
  • [7] STARTING THE CELL-CYCLE - WHATS THE POINT
    CROSS, FR
    [J]. CURRENT OPINION IN CELL BIOLOGY, 1995, 7 (06) : 790 - 797
  • [8] DOHLMAN HG, 2001, IN PRESS ANN REV BIO
  • [9] Edwards MC, 1997, GENETICS, V147, P1063
  • [10] Pheromone response, mating and cell biology
    Elion, EA
    [J]. CURRENT OPINION IN MICROBIOLOGY, 2000, 3 (06) : 573 - 581