Feasting, fasting and fermenting: Glucose sensing in yeast and other cells

Trends in Genetics

Volumn 15, Issue 1, 1999, Pages 29-33

  Johnston, Mark ^a  

^a WASHINGTON UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CHEMOSENSITIVITY; FERMENTATION; GENE EXPRESSION REGULATION; GENE REPRESSION; GLUCOSE METABOLISM; NONHUMAN; PRIORITY JOURNAL; REVIEW; SACCHAROMYCES CEREVISIAE; SIGNAL TRANSDUCTION;

ADENOSINE TRIPHOSPHATE; ANIMALS; CARRIER PROTEINS; EATING; ENERGY METABOLISM; FASTING; FERMENTATION; FUNGAL PROTEINS; GENE EXPRESSION REGULATION, FUNGAL; GLUCOSE; HUMANS; MACROMOLECULAR SUBSTANCES; MEMBRANE PROTEINS; MODELS, BIOLOGICAL; REPRESSOR PROTEINS; SACCHAROMYCES CEREVISIAE; SIGNAL TRANSDUCTION; TRANSCRIPTION FACTORS;

EID: 0032941868     PISSN: 01689525     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0168-9525(98)01637-0     Document Type: Review

References (62)

1. Magasanik B. Catabolite repression. Cold Spring Harbor Symp. Quant. Biol. 26:1961;249-256.
2. Ullmann A. Catabolite repression: a story without end. Res. Microbiol. 147:1996;455-458.
3. Cereghino G.P., Scheffler I.E. Genetic analysis of glucose regulation in Saccharomyces cerevisiae: control of transcription versus mRNA turnover. EMBO J. 15:1996;363-374.
4. Vallari R.C.et al. Glucose repression of the yeast ADH2 gene occurs through multiple mechanisms, including control of the protein synthesis of its transcriptional activator, ADR1. Mol. Cell. Biol. 12:1992;1663-1673.
5. Jiang H.et al. Two glucose sensing/signaling pathways stimulate glucose-induced inactivation of maltose permease in Saccharomyces. Mol. Biol. Cell. 8:1997;1293-1304.
6. Lagunas R. Energetic irrelevance of aerobiosis for S. cerevisiae growing on sugars. Mol. Cell. Biochem. 27:1979;139-146.
7. Samuel D. Investigation of ancient egyptian baking and brewing methods by correlative microscopy. Science. 273:1996;488-490.
8. Yin Z.et al. Multiple signalling pathways trigger the exquisite sensitivity of yeast gluconeogenic mRNAs to glucose. Mol. Micro. 20:1996;751-764.
9. Ostling J.et al. Functional domains in the Mig1 repressor Mol. Cell. Biol. 16:1996;753-761.
10. Hardie D.G.et al. The AMP-activated/Snf1 protein kinase subfamily - metaboloid sensors of the eukaryotic cell. Annu. Rev. Biochem. 67:1998;821-855.
11. Yang X.et al. A family of proteins containing a conserved domain that mediates interaction with the yeast SNF1 protein kinase complex. EMBO J. 13:1994;5878-5886.
12. Tu J., Carlson M. REG1 binds to protein phosphatase type 1 and regulates glucose repression in Saccharomyces cerevisiae. EMBO J. 14:1995;5939-5946.
13. Lutfiyya L.L., Johnston M. Two zinc-finger-containing repressors are responsible for glucose repression of SUC2 Expression. Mol. Cell. Biol. 16:1996;4790-4797.
14. Treitel M.A., Carlson M. Repression by SSN6-TUP1 is directed by MIG1, a repressor/activator protein. Proc. Natl. Acad. Sci. U. S. A. 92:1995;3132-3136.
15. Lutfiyya, L.L. and Johnston, M. Characterization of the three related glucose repressors and genes they regulate in Saccahromyces cerevisiae. Genetics (in Press).
16. Devit M.et al. Regulated nuclear translocation of the Mig1 glucose repressor. Mol. Biol. Cell. 8:1997;1603-1618.
17. Woods A.et al. Yeast SNF1 is functionally related to mammalian AMP-activated protein kinase and regulates Acetyl-CoA Carboxylase in vivo. J. Biol. Chem. 269:1994;19509-19515.
18. Wilson W.A.et al. Glucose repression/derepression in budding yeast: SNF1 kprotein kinase is activated by phosphorylation under derepressing conditions, and this correlates with a high AMP:ATP ratio. Curr. Biol. 6:1996;1426-1434.
19. Treitel M.A.et al. Snf1 protein kinase regulates phosphorylation of the Mig1 repressor in Saccharomyces cerevisiae. Mol. Cell. Biol. 18:1998;6273-6280.
20. Ludin K.et al. Glucose-regulated interaction of a regulatory subunit of protein phosphatase 1 with the Snf1 protein kinase in Saccharomyces cerevisiae. Proc. Natl. Acad. Sci. U. S. A. 95:1998;6245-6250.
21. Jiang, R. and Carlson, M. (1996) Glucose regulates protein interactions within the yeast SNF1 protein kinase complex. Genes Dev. 10, 3105-311.
22. Jiang R., Carlson M. The Snf1 protein kinase and its activating subunit, Snf4, interact with distinct domains of the Sip1/Sip2/Gal83 component in the kinase complex. Mol. Cell. Biol. 17:1997;2099-2106.
23. Tu J., Carlson M. The GLC7 type 1 protein phosphatase is required for glucose repression in Saccharomyces cerevisiae. Mol. Cell. Biol. 14:1994;6789-6796.
24. Estruch F.et al. N-terminal mutations modulate yeast SNF1 protein kinase function. Genetics. 132:1992;639-650.
25. Woods A.et al. Yeast SNF1 is functionally related to mammalian AMP-activated protein kinase and regulates acetyl-CoA carboxylase in vivo. J. Biol. Chem. 269:1994;19509-19515.
26. Stapleton D.et al. Mammalian 5'-AMP-activated protein kinase non-catalytic subunits are homologs of proteins that interact with yeast Snf1 protein kinase. J. Biol. Chem. 269:1994;29343-29346.
27. De Winde J.H.et al. Differential requirement of the yeast sugar kinases for sugar sensing in establishing the catabolite-repressed state. Eur. J. Biochem. 241:1996;633-643.
28. Gancedo C., Gancedo M. Phosphorylation of 3-O-methyl-D-glucose and catabolite repression in yeast. Eur. J. Biochem. 148:1985;593-597.
29. Gancedo J.M. Carbon catabolite repression in yeast. Eur. J. Biochem. 206:1992;297-313.
30. Meijer M.M.C.et al. Glucose repression in Saccharomcyes cerevisiae is related to the glucose concentration rather than the glucose flux. J. Biol. Chem. 273:1998;24102-24107.
31. Hardie D.G., Carling D. The AMP-activated protein kinase. Fuel guage of the mammalian cell? Eur. J. Biochem. 246:1997;259-273.
32. Halford N.G.et al. Investigating the role of plant SNF1-related protein kinases. Biochem. Soc. Trans. 22:1994;953-957.
33. Foretz M.et al. AMP-activated protein kinase inhibits the glucose-activated expression of fatty acid synthase gene in rat hepatocytes. J. Biol. Chem. 273:1998;14767-14771.
34. Leclerc I.et al. The 5'-AMP-activated protein kinase inhibits the transcriptional stimulation by glucose in liver cells, acting through the glucose response complex. FEBS Lett. 431:1998;180-184.
35. Muller S.et al. Different internal metabolites trigger the induction of glycolytic gene expression in Saccharomyces cerevisiae. J. Bacteriol. 177:1995;4517-4519.
36. Özcan S., Johnston M. Three different regulatory mechanisms enable yeast hexose transporter (HXT) genes to be induced by different levels of glucose. Mol. Cell. Biol. 15:1995;1564-1572.
37. Özcan S.et al. Rgt1p of S. cerevisiae, a key regulator of glucose-induced genes, is both an activator and repressor of transcription. Mol. Cell. Biol. 16:1996;6419-6426.
38. Li F., Johnston M. Grr1 of Saccharomyces cerevisiae is connected to the ubiquitin proteolysis machinery through Skp1: coupling glucose sensing to gene expression and the cell cycle. EMBO J. 16:1997;101-110.
39. Kishi T.et al. Grr1 functions in the ubiquitin pathway in Saccharomyces cerevisiae through association with Skp1. Mol. Gen. Genet. 257:1998;143-148.
40. Kruckeberg A.L. The hexose transporter family of Saccharomyces cerevisiae. Arch. Microbiol. 166:1996;283-292.
41. Boles E., Hollenberg C.P. The molecular genetics of hexose transport in yeasts. FEMS Micro. Rev. 21:1997;85-111.
42. Özcan S.et al. Two glucose transporters in Saccharomyces cerevisiae are glucose sensors that generate a signal for induction of gene expression. Proc. Natl. Acad. Sci. U. S. A. 93:1996;12428-12432.
43. Reifenberger E.et al. Kinetic characterization of individual hexose transporters of Saccharomyces cerevisiae and their relation to the triggering mechanisms of glucose repression. Eur. J. Biochem. 245:1997;324-333.
44. Özcan S., Johnston M. Two different repressors collaborate to restrict expression of yeast glucose transporter genes HXT2 and HXT4 to low levels of glucose. Mol. Cell. Biol. 16:1996;5536-5545.
45. Bai C.et al. SKP1 connects cell cycle regulators to the ubiquitin proteolysis machinery through a novel motif, the F-box. Cell. 86:1996;263-274.
46. Skowyra D.et al. F-box proteins are receptors that recruit phosphorylated substrates to the SCF ubiquitin-ligase complex. Cell. 91:1997;209-219.
47. Patton E.E.et al. Combinatorial control in ubiquitin-dependent proteolysis: don't Skp the F-box hypothesis. Trends Genet. 14:1998;236-243.
48. Barral Y.et al. G1 cyclin turnover and nutrient uptake are controlled by a common pathway in yeast. Genes Dev. 9:1995;399-409.
49. Grr1 complex. EMBO J. 18:1998;5360-5373.
50. Johnson E.S., Blobel G. Ubc9 is the conjugating enzyme for the ubiquitin-like protein Smt3p. J. Biol. Chem. 272:1997;26799-26802.
51. Cdc4 complex. Genes Dev. 12:1998;914-926.
52. Wendell D.L., Bisson L.F. Expression of high-affinity glucose transport protein Hxt2p of Saccharomyces cerevisiae is both repressed and induced by glucose and appears to be regulated posttranslationally. J. Bacteriol. 176:1994;3730-3737.
53. Marshall-Carlson L.et al. Mutational analysis of the SNF3 glucose transporter of Saccharomyces cerevisiae. Mol. Cell. Biol. 10:1990;1105-1115.
54. Özcan S.et al. Glucose sensing and signaling by two glucose receptors in the yeast Saccharomyces cerevisiae. EMBO J. 17:1998;2566-2573.
55. Coons D.M.et al. The C-terminal domain of Snf3p is sufficient to complement the growth defect of snf3 null mutations in Saccharomyces cerevisiae: SNF3 functions in glucose recognition. Yeast. 13:1997;9-20.
56. Vagnoli P.et al. The C-terminal domain of Snf3p mediates glucose-responsive signal transduction in Saccharomyces cerevisiae. FEMS Micro. Lett. 160:1998;31-36.
57. Efrat S.et al. The pancreatic beta-cell glucose sensor. Trends Biochem. Sci. 19:1994;535-538.
58. Newgard C.B., McGarry J.D. Metabolic coupling factors in pancreatic beta-cell signal transduction. Ann. Rev. Biochem. 64:1995;689-719.
59. Madi L.et al. rco-3, a gene involved in glucose transport and conidiation in Neurospora crassa. Genetics. 146:1997;499-508.
60. Ruegger M.et al. The TIR1 protein of Arabidopsis functions in auxin response and is related to human SKP2 and yeast Grr1p. Genes Dev. 12:1998;198-207.
61. Xie D-X.et al. COI1: An Arabidopsis gene required for jasmonate-regulated defense and fertility. Science. 280:1998;1091-1094.
62. Zhang H.et al. p19Skp1 and p45Skp2 are essential elements of the cyclin A-CDK2 S phase kinase. Cell. 82:1995;915-925.