The SH3-domain protein Bem1 coordinates mitogen-activated protein kinase cascade activation with cell cycle control in Saccharomyces cerevisiae
- PMID: 8754808
- PMCID: PMC231406
- DOI: 10.1128/MCB.16.8.4095
The SH3-domain protein Bem1 coordinates mitogen-activated protein kinase cascade activation with cell cycle control in Saccharomyces cerevisiae
Abstract
The mating mitogen-activated protein kinase (MAPK) cascade has three major outputs prior to fusion: transcriptional activation of many genes, cell cycle arrest in the G1 phase, and polarized growth. Bem1 localizes near the cortical actin cytoskeleton and is essential for polarized growth during mating. Here we show that Bem1 is required for efficient signal transduction and coordinates MAPK cascade activation with G1 arrest and mating. bem1delta null mutants are defective in G1 arrest and transcriptional activation in response to mating pheromone. Bem1 protein stimulates Fus3 (MAPK) activity and associates with Ste5, the tethering protein essential for activation of the MAPK kinase kinase Ste11. Bem1-Ste5 complexes also contain Ste11, Ste7 (MAPK kinase), and Fus3, suggesting that Ste5 localizes the MAPK cascade to Bem1. Strikingly, Bem1 also copurifies with Far1, a Fus3 substrate required for G1 arrest and proper polarized growth during mating. These and other results suggest that Bem1 may cross-link the Ste5-MAPK cascade complex to upstream activators and specific downstream substrates at the shmoo tip, thus enabling efficient circuitry for G1 arrest and mating.
Similar articles
-
Ste5 tethers multiple protein kinases in the MAP kinase cascade required for mating in S. cerevisiae.Cell. 1994 Aug 12;78(3):499-512. doi: 10.1016/0092-8674(94)90427-8. Cell. 1994. PMID: 8062390
-
Functional binding between Gbeta and the LIM domain of Ste5 is required to activate the MEKK Ste11.Curr Biol. 1998 Feb 26;8(5):267-78. doi: 10.1016/s0960-9822(98)70108-3. Curr Biol. 1998. PMID: 9501067
-
Loss of sustained Fus3p kinase activity and the G1 arrest response in cells expressing an inappropriate pheromone receptor.Mol Cell Biol. 1996 Aug;16(8):4478-85. doi: 10.1128/MCB.16.8.4478. Mol Cell Biol. 1996. PMID: 8754848 Free PMC article.
-
Pheromone response, mating and cell biology.Curr Opin Microbiol. 2000 Dec;3(6):573-81. doi: 10.1016/s1369-5274(00)00143-0. Curr Opin Microbiol. 2000. PMID: 11121776 Review.
-
MAP kinase pathways in yeast: for mating and more.Cell. 1995 Jan 27;80(2):187-97. doi: 10.1016/0092-8674(95)90402-6. Cell. 1995. PMID: 7834739 Review. No abstract available.
Cited by
-
A Protein-Protein Interaction Analysis Suggests a Wide Range of New Functions for the p21-Activated Kinase (PAK) Ste20.Int J Mol Sci. 2023 Nov 2;24(21):15916. doi: 10.3390/ijms242115916. Int J Mol Sci. 2023. PMID: 37958899 Free PMC article.
-
Lrg1p Is a Rho1 GTPase-activating protein required for efficient cell fusion in yeast.Genetics. 2004 Oct;168(2):733-46. doi: 10.1534/genetics.104.028027. Genetics. 2004. PMID: 15514049 Free PMC article.
-
MAP kinase pathways in the yeast Saccharomyces cerevisiae.Microbiol Mol Biol Rev. 1998 Dec;62(4):1264-300. doi: 10.1128/MMBR.62.4.1264-1300.1998. Microbiol Mol Biol Rev. 1998. PMID: 9841672 Free PMC article. Review.
-
Quantitative measurement of protein relocalization in live cells.Biophys J. 2013 Feb 5;104(3):727-36. doi: 10.1016/j.bpj.2012.12.030. Biophys J. 2013. PMID: 23442923 Free PMC article.
-
Cdc42: An essential Rho-type GTPase controlling eukaryotic cell polarity.Microbiol Mol Biol Rev. 1999 Mar;63(1):54-105. doi: 10.1128/MMBR.63.1.54-105.1999. Microbiol Mol Biol Rev. 1999. PMID: 10066831 Free PMC article. Review.
References
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Molecular Biology Databases