Saccharomyces cerevisiae Mpt5p interacts with Sst2p and plays roles in pheromone sensitivity and recovery from pheromone arrest

SST2 plays an important role in the sensitivity of yeast cells to pheromone and in recovery from pheromone-induced G1 arrest. Recently, a family of Sst2p homologs that act as GTPase-activating proteins (GAPs) for G alpha subunits has been identified. We have identified an interaction between Sst2p and the previously identified Mpt5p by using the two-hybrid system. Loss of Mpt5p function resulted in a temperature-sensitive growth phenotype, an increase in pheromone sensitivity, and a defect in recovery from pheromone-induced G1 arrest, although the effects on pheromone response and recovery were mild in comparison to those of sst2 mutants. Overexpression of either Sst2p or Mpt5p promoted recovery from G1 arrest. Promotion of recovery by overexpression of Mpt5p required Sst2p, but the effect of overexpression of Sst2p was only partially dependent on Mpt5p. Mpt5p was also found to interact with the mitogen-activated protein kinase homologs Fus3p and Kss1p, and an mpt5 mutation was able to suppress the pheromone arrest and mating defects of a fus3 mutant. Because either mpt5 or cln3 mutations suppressed the fus3 phenotypes, interactions of Mpt5p with the G1 cyclins and Cdc28p were tested. An interaction between Mpt5p and Cdc28p was detected. We discuss these results with respect to a model in which Sst2p plays a role in pheromone sensitivity and recovery that acts through Mpt5p in addition to a role as a G alpha GAP suggested by the analysis of the Sst2p homologs.

[1]  S. Pelech,et al.  Mitogen-activated protein kinases: versatile transducers for cell signaling. , 1992, Trends in biochemical sciences.

[2]  R. W. Davis,et al.  A dominant truncation allele identifies a gene, STE20, that encodes a putative protein kinase necessary for mating in Saccharomyces cerevisiae. , 1993, Proceedings of the National Academy of Sciences of the United States of America.

[3]  B. Futcher,et al.  The Cln3‐Cdc28 kinase complex of S. cerevisiae is regulated by proteolysis and phosphorylation. , 1992, The EMBO journal.

[4]  David Y. Thomas,et al.  The STE4 and STE18 genes of yeast encode potential β and γ subunits of the mating factor receptor-coupled G protein , 1989, Cell.

[5]  K. Doi,et al.  Cloning and nucleotide sequence of the CDC23 gene of Saccharomyces cerevisiae. , 1990, Gene.

[6]  Comparison of dose-response curves for alpha factor-induced cell division arrest, agglutination, and projection formation of yeast cells. Implication for the mechanism of alpha factor action. , 1983, The Journal of biological chemistry.

[7]  S. Fields,et al.  The yeast STE12 protein binds to the DNA sequence mediating pheromone induction. , 1989, Proceedings of the National Academy of Sciences of the United States of America.

[8]  Bee-Na Lee,et al.  Overexpression of fIbA, an early regulator of Aspergillus asexual sporulation, leads to activation of brIA and premature initiation of development , 1994, Molecular microbiology.

[9]  P. Macdonald,et al.  The Drosophila pumilio gene: an unusually long transcription unit and an unusual protein. , 1992, Development.

[10]  G. Sprague,,et al.  Protein-protein interactions in the yeast pheromone response pathway: Ste5p interacts with all members of the MAP kinase cascade. , 1994, Genetics.

[11]  Curt Wittenberg,et al.  An essential G1 function for cyclin-like proteins in yeast , 1989, Cell.

[12]  R. Sikorski,et al.  A system of shuttle vectors and yeast host strains designed for efficient manipulation of DNA in Saccharomyces cerevisiae. , 1989, Genetics.

[13]  G. Fink,et al.  FUS3 encodes a cdc2+/CDC28-related kinase required for the transition from mitosis into conjugation , 1990, Cell.

[14]  D. Ecker,et al.  Chemical synthesis and expression of a cassette adapted ubiquitin gene. , 1987, The Journal of biological chemistry.

[15]  P. Farabaugh,et al.  Nucleotide sequence of a yeast Ty element: evidence for an unusual mechanism of gene expression. , 1985, Proceedings of the National Academy of Sciences of the United States of America.

[16]  F. Cross Cell cycle arrest caused by CLN gene deficiency in Saccharomyces cerevisiae resembles START-I arrest and is independent of the mating-pheromone signalling pathway , 1990, Molecular and cellular biology.

[17]  Jae-Hyuk Yu,et al.  The Aspergillus FlbA RGS domain protein antagonizes G protein signaling to block proliferation and allow development. , 1996, The EMBO journal.

[18]  L. Breeden,et al.  Regulation of the yeast HO gene. , 1985, Cold Spring Harbor symposia on quantitative biology.

[19]  G. Fink,et al.  FUS3 represses CLN1 and CLN2 and in concert with KSS1 promotes signal transduction. , 1991, Proceedings of the National Academy of Sciences of the United States of America.

[20]  C. Chien A novel genetic system to detect protein-protein interactions , 1991 .

[21]  M. Whiteway,et al.  Theprotein kinase homologue Ste2Opisrequired tolink theyeastpheromone response G-protein flysubunits to downstream signalling components , 1992 .

[22]  J. Kurjan,et al.  The yeast SCG1 gene: A Gα-like protein implicated in the a- and α-factor response pathway , 1987, Cell.

[23]  C. Bruschi,et al.  The DNA sequence of a 7941 bp fragment of the left arm of chromosome VII of Saccharomyces cerevisiae contains four open reading frames including the multicopy suppressor gene of the pop2 mutation and a putative serine/threonine protein kinase gene , 1995, Yeast.

[24]  F. Klis,et al.  Targeting of a heterologous protein to the cell wall of Saccharomyces cerevisiae , 1993, Yeast.

[25]  F. Cross,et al.  Saccharomyces cerevisiae G1 cyclins differ in their intrinsic functional specificities , 1996, Molecular and cellular biology.

[26]  M. Whiteway,et al.  The protein kinase homologue Ste20p is required to link the yeast pheromone response G‐protein beta gamma subunits to downstream signalling components. , 1992, The EMBO journal.

[27]  J. Kurjan The pheromone response pathway in Saccharomyces cerevisiae. , 1993, Annual review of genetics.

[28]  R. Lehmann,et al.  Pumilio is essential for function but not for distribution of the Drosophila abdominal determinant Nanos. , 1992, Genes & development.

[29]  A. Gilman,et al.  RGS4 and GAIP are GTPase-activating proteins for Gq alpha and block activation of phospholipase C beta by gamma-thio-GTP-Gq alpha. , 1997, Proceedings of the National Academy of Sciences of the United States of America.

[30]  R. K. Chan,et al.  Isolation and genetic analysis of Saccharomyces cerevisiae mutants supersensitive to G1 arrest by a factor and alpha factor pheromones , 1982, Molecular and cellular biology.

[31]  A. Goffeau,et al.  VII. Yeast sequencing reports. The YGL023 gene encodes a putative regulatory protein , 1991, Yeast.

[32]  G. Fink,et al.  Two genes required for cell fusion during yeast conjugation: evidence for a pheromone-induced surface protein , 1987, Molecular and cellular biology.

[33]  I. Herskowitz,et al.  Direct inhibition of the yeast cyclin-dependent kinase Cdc28-Cln by Far1. , 1994, Science.

[34]  I. Herskowitz,et al.  Signal transduction during pheromone response in yeast. , 1991, Annual review of cell biology.

[35]  B. Errede,et al.  STE12, a protein involved in cell-type-specific transcription and signal transduction in yeast, is part of protein-DNA complexes. , 1989, Genes & development.

[36]  Y. Kang,et al.  Effects of expression of mammalian G alpha and hybrid mammalian-yeast G alpha proteins on the yeast pheromone response signal transduction pathway , 1990, Molecular and cellular biology.

[37]  S. Fields,et al.  Pheromone-dependent phosphorylation of the yeast STE12 protein correlates with transcriptional activation. , 1991, Genes & development.

[38]  E. Chen,et al.  Shuttle mutagenesis: a method of transposon mutagenesis for Saccharomyces cerevisiae. , 1986, Proceedings of the National Academy of Sciences of the United States of America.

[39]  B. Errede,et al.  The proliferation of MAP kinase signaling pathways in yeast. , 1995, Current opinion in cell biology.

[40]  B. Futcher,et al.  Comparison of the Saccharomyces cerevisiae G1 cyclins: Cln3 may be an upstream activator of Cln1, Cln2 and other cyclins. , 1993, The EMBO journal.

[41]  M. Ciriacy,et al.  Glucose uptake and catabolite repression in dominant HTR1 mutants of Saccharomyces cerevisiae , 1993, Journal of bacteriology.

[42]  G. Fink,et al.  A role for autophosphorylation revealed by activated alleles of FUS3, the yeast MAP kinase homolog. , 1994, Molecular biology of the cell.

[43]  J. Thorner,et al.  A putative protein kinase overcomes pheromone-induced arrest of cell cycling in S. cerevisiae , 1989, Cell.

[44]  S. Fields,et al.  Elimination of false positives that arise in using the two-hybrid system. , 1993, BioTechniques.

[45]  I. Herskowitz,et al.  Putting the HO gene to work: practical uses for mating-type switching. , 1991, Methods in enzymology.

[46]  D. I. Johnson,et al.  Genetic relationships between the G protein beta gamma complex, Ste5p, Ste20p and Cdc42p: investigation of effector roles in the yeast pheromone response pathway. , 1996, Genetics.

[47]  E. Elion,et al.  FUS3 phosphorylates multiple components of the mating signal transduction cascade: evidence for STE12 and FAR1. , 1993, Molecular biology of the cell.

[48]  J. Thorner,et al.  Sst2, a negative regulator of pheromone signaling in the yeast Saccharomyces cerevisiae: expression, localization, and genetic interaction and physical association with Gpa1 (the G-protein alpha subunit) , 1996, Molecular and cellular biology.

[49]  B. Futcher,et al.  Far1 and Fus3 Link the Mating Pheromone Signal Transduction Pathway to Three G1-Phase Cdc28 Kinase Complexes , 1993, Molecular and cellular biology.

[50]  R. K. Chan,et al.  Physiological characterization of Saccharomyces cerevisiae mutants supersensitive to G1 arrest by a factor and alpha factor pheromones , 1982, Molecular and cellular biology.

[51]  R. Wharton,et al.  Binding of pumilio to maternal hunchback mRNA is required for posterior patterning in drosophila embryos , 1995, Cell.

[52]  S. Elledge,et al.  The p21 Cdk-interacting protein Cip1 is a potent inhibitor of G1 cyclin-dependent kinases , 1993, Cell.

[53]  E. Elion,et al.  The MAP kinase Fus3 associates with and phosphorylates the upstream signaling component Ste5. , 1994, Genes & development.

[54]  M. Dante,et al.  Multifunctional yeast high-copy-number shuttle vectors. , 1992, Gene.

[55]  S. Fields,et al.  The two-hybrid system: a method to identify and clone genes for proteins that interact with a protein of interest. , 1991, Proceedings of the National Academy of Sciences of the United States of America.

[56]  Gustav Ammerer,et al.  FAR1 links the signal transduction pathway to the cell cycle machinery in yeast , 1993, Cell.

[57]  S. Pelech,et al.  Definition of a consensus sequence for peptide substrate recognition by p44mpk, the meiosis-activated myelin basic protein kinase. , 1991, The Journal of biological chemistry.

[58]  M. Wigler,et al.  Complexes between STE5 and components of the pheromone-responsive mitogen-activated protein kinase module. , 1994, Proceedings of the National Academy of Sciences of the United States of America.

[59]  D. Shore,et al.  A RAP1-interacting protein involved in transcriptional silencing and telomere length regulation. , 1992, Genes & development.

[60]  H. Dohlman,et al.  Inhibition of G-protein signaling by dominant gain-of-function mutations in Sst2p, a pheromone desensitization factor in Saccharomyces cerevisiae , 1995, Molecular and cellular biology.

[61]  J. Thorner,et al.  RGS Proteins and Signaling by Heterotrimeric G Proteins* , 1997, The Journal of Biological Chemistry.

[62]  K. Arai,et al.  GPA1, a haploid-specific essential gene, encodes a yeast homolog of mammalian G protein which may be involved in mating factor signal transduction , 1987, Cell.

[63]  F. Cross,et al.  DAF1, a mutant gene affecting size control, pheromone arrest, and cell cycle kinetics of Saccharomyces cerevisiae , 1988, Molecular and cellular biology.

[64]  E. Elion,et al.  Ste5 tethers multiple protein kinases in the MAP kinase cascade required for mating in S. cerevisiae , 1994, Cell.

[65]  B. Errede,et al.  MAP kinase-related FUS3 from S. cerevisiae is activated by STE7 in vitro , 1993, Nature.

[66]  R. Rothstein One-step gene disruption in yeast. , 1983, Methods in enzymology.

[67]  J. Kurjan,et al.  Pheromonal regulation and sequence of the Saccharomyces cerevisiae SST2 gene: a model for desensitization to pheromone. , 1987, Molecular and cellular biology.

[68]  David,et al.  RGS4 and GAIP are GTPase-activating proteins for G q (cid:97) and block activation of phospholipase C (cid:98) by (cid:103) -thio-GTP-G q (cid:97) , 1997 .

[69]  R. Iyengar There Are GAPS and There Are GAPS , 1997, Science.

[70]  R. Deschenes,et al.  Vectors for the inducible overexpression of glutathione S‐transferase fusion proteins in yeast , 1993, Yeast.

[71]  M. Farquhar,et al.  GAIP, a protein that specifically interacts with the trimeric G protein G alpha i3, is a member of a protein family with a highly conserved core domain. , 1995, Proceedings of the National Academy of Sciences of the United States of America.

[72]  M. Smith,et al.  Oligonucleotide-directed mutagenesis: a simple method using two oligonucleotide primers and a single-stranded DNA template. , 1984, DNA.

[73]  T. Chibazakura,et al.  Molecular analysis of POP2 gene, a gene required for glucose-derepression of gene expression in Saccharomyces cerevisiae , 2022 .