A signaling mucin at the head of the Cdc42- and MAPK-dependent filamentous growth pathway in yeast

被引:168
作者
Cullen, PJ
Sabbagh, W
Graham, E
Irick, MM
van Olden, EK
Neal, C
Delrow, J
Bardwell, L
Sprague, GF [1 ]
机构
[1] Univ Oregon, Inst Mol Biol, Eugene, OR 97403 USA
[2] Univ Calif Irvine, Dept Dev & Cell Biol, Irvine, CA 92697 USA
[3] Fred Hutchinson Canc Res Ctr, Seattle, WA 98109 USA
关键词
morphogenesis; cell polarity; signal transduction; pseudohyphal growth; specificity;
D O I
10.1101/gad.1178604
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Signaling molecules such as Cdc42 and mitogen-activated protein kinases (MAPKs) can function in multiple pathways in the same cell. Here, we propose one mechanism by which such factors may be directed to function in a particular pathway such that a specific response is elicited. Using genomic approaches, we identify a new component of the Cdc42- and MAPK-dependent signaling pathway that regulates filamentous growth (FG) in yeast. This factor, called Msb2, is a FG-pathway-specific factor that promotes differential activation of the MAPK for the FG pathway, Kss1. Msb2 is localized to polarized sites on the cell surface and interacts with Cdc42 and with the osmosensor for the high osmolarity glycerol response (HOG) pathway, Sho1. Msb2 is glycosylated and is a member of the mucin family, proteins that in mammalian cells promote disease resistance and contribute to metastasis in cancer cells. Remarkably, loss of the mucin domain of Msb2 causes hyperactivity of the FG pathway, demonstrating an inhibitory role for mucin domains in MAPK pathway activation. Taken together, our data suggest that Msb2 is a signaling mucin that interacts with general components, such as Cdc42 and Sho1, to promote their function in the FG pathway.
引用
收藏
页码:1695 / 1708
页数:14
相关论文
共 76 条
[1]   The biological role of mucins in cellular interactions and immune regulation: prospects for cancer immunotherapy [J].
Agrawal, B ;
Gendler, SJ ;
Longenecker, BM .
MOLECULAR MEDICINE TODAY, 1998, 4 (09) :397-403
[2]  
Agrawal B, 1998, CANCER RES, V58, P4079
[3]   A Bayesian framework for the analysis of microarray expression data: regularized t-test and statistical inferences of gene changes [J].
Baldi, P ;
Long, AD .
BIOINFORMATICS, 2001, 17 (06) :509-519
[4]   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
[5]   Repression of yeast Ste12 transcription factor by direct binding of unphosphorylated Kss1 MAPK and its regulation by the Ste7 MEK [J].
Bardwell, L ;
Cook, JG ;
Voora, D ;
Baggott, DM ;
Martinez, AR ;
Thorner, J .
GENES & DEVELOPMENT, 1998, 12 (18) :2887-2898
[6]   A SER THR-RICH MULTICOPY SUPPRESSOR OF A CDC24 BUD EMERGENCE DEFECT [J].
BENDER, A ;
PRINGLE, JR .
YEAST, 1992, 8 (04) :315-323
[7]   CONTROLLING THE FALSE DISCOVERY RATE - A PRACTICAL AND POWERFUL APPROACH TO MULTIPLE TESTING [J].
BENJAMINI, Y ;
HOCHBERG, Y .
JOURNAL OF THE ROYAL STATISTICAL SOCIETY SERIES B-STATISTICAL METHODOLOGY, 1995, 57 (01) :289-300
[8]   MAPK signaling specificity: it takes two to tango [J].
Breitkreutz, A ;
Tyers, M .
TRENDS IN CELL BIOLOGY, 2002, 12 (06) :254-257
[9]   MAPK specificity in the yeast pheromone response independent of transcriptional activation [J].
Breitkreutz, A ;
Boucher, L ;
Tyers, M .
CURRENT BIOLOGY, 2001, 11 (16) :1266-+
[10]   Cell signaling through membrane mucins [J].
Carraway, KL ;
Ramsauer, VP ;
Haq, B ;
Carraway, CAC .
BIOESSAYS, 2003, 25 (01) :66-71