Function and evolution of 'green' GSK3/Shaggy-like kinases

Trends in Plant Science

Volumn 17, Issue 1, 2012, Pages 39-46

  Saidi, Younousse ^a   Hearn, Timothy J ^a   Coates, Juliet C ^a  

^a UNIVERSITY OF BIRMINGHAM   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

GLYCOGEN SYNTHASE KINASE 3; PHYTOHORMONE; VEGETABLE PROTEIN;

AMINO ACID SEQUENCE; ANGIOSPERM; ARABIDOPSIS; CHEMISTRY; ENZYMOLOGY; EVOLUTION; GENETICS; METABOLISM; MOLECULAR GENETICS; PHYSIOLOGICAL STRESS; PHYSIOLOGY; REVIEW; SEQUENCE ALIGNMENT; SIGNAL TRANSDUCTION;

AMINO ACID SEQUENCE; ANGIOSPERMS; ARABIDOPSIS; BIOLOGICAL EVOLUTION; GLYCOGEN SYNTHASE KINASE 3; MOLECULAR SEQUENCE DATA; PLANT GROWTH REGULATORS; PLANT PROTEINS; SEQUENCE ALIGNMENT; SIGNAL TRANSDUCTION; STRESS, PHYSIOLOGICAL;

ALGAE; AMOEBA (GENUS); ANIMALIA; ARABIDOPSIS; DICOTYLEDONEAE; EMBRYOPHYTA; EUKARYOTA; FUNGI; MAGNOLIOPHYTA; PROTISTA;

EID: 84855603860     PISSN: 13601385     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tplants.2011.10.002     Document Type: Review

References (70)

1. Cohen P., et al. Separation and characterisation of glycogen synthase kinase 3, glycogen synthase kinase 4 and glycogen synthase kinase 5 from rabbit skeletal muscle. Eur. J. Biochem. 1982, 124:21-35.
2. Frame S., Cohen P. GSK3 takes centre stage more than 20 years after its discovery. Biochem. J. 2001, 359:1-16.
3. Jope R.S., Johnson G.V. The glamour and gloom of glycogen synthase kinase-3. Trends Biochem. Sci. 2004, 29:95-102.
4. Logan C.Y., Nusse R. The Wnt signaling pathway in development and disease. Annu. Rev. Cell Dev. Biol. 2004, 20:781-810.
5. Petersen C.P., Reddien P.W. Wnt signaling and the polarity of the primary body axis. Cell 2009, 139:1056-1068.
6. Harwood A.J., et al. Glycogen synthase kinase 3 regulates cell fate in Dictyostelium. Cell 1995, 80:139-148.
7. Kim L., Kimmel A.R. GSK3 at the edge: regulation of developmental specification and cell polarization. Curr. Drug Targets 2006, 7:1411-1419.
8. Doble B.W., Woodgett J.R. GSK-3: tricks of the trade for a multi-tasking kinase. J. Cell Sci. 2003, 116:1175-1186.
9. Jonak C., Hirt H. Glycogen synthase kinase 3/SHAGGY-like kinases in plants: an emerging family with novel functions. Trends Plant Sci. 2002, 7:457-461.
10. de la Fuente van Bentem S., et al. Site-specific phosphorylation profiling of Arabidopsis proteins by mass spectrometry and peptide chip analysis. J. Proteome Res. 2008, 7:2458-2470.
11. Bourouis M., et al. An early embryonic product of the gene shaggy encodes a serine threonine protein-kinase related to the Cdc28/Cdc2+ subfamily. EMBO J. 1990, 9:2877-2884.
12. Li J., et al. Conservation of function between mammalian and plant steroid 5alpha-reductases. Proc. Natl. Acad. Sci. U.S.A. 1997, 94:3554-3559.
13. Kim T.W., Wang Z.Y. Brassinosteroid signal transduction from receptor kinases to transcription factors. Annu. Rev. Plant Biol. 2010, 61:681-704.
14. Clouse S.D. Brassinosteroid signal transduction: from receptor kinase activation to transcriptional networks regulating plant development. Plant Cell 2011, 23:1219-1230.
15. Yang C.J., et al. The mechanisms of brassinosteroids' action: from signal transduction to plant development. Mol. Plant 2011, 4:588-600.
16. Gudesblat G.E., Russinova E. Plants grow on brassinosteroids. Curr. Opin. Plant Biol. 2011, 14:530-537.
17. Li J., et al. BIN2, a new brassinosteroid-insensitive locus in Arabidopsis. Plant Physiol. 2001, 127:14-22.
18. Li J., Nam K.H. Regulation of brassinosteroid signaling by a GSK3/SHAGGY-like kinase. Science 2002, 295:1299-1301.
19. Perez-Perez J.M., et al. The UCU1 Arabidopsis gene encodes a SHAGGY/GSK3-like kinase required for cell expansion along the proximodistal axis. Dev. Biol. 2002, 242:161-173.
20. Choe S., et al. Arabidopsis brassinosteroid-insensitive dwarf12 mutants are semidominant and defective in a glycogen synthase kinase 3beta-like kinase. Plant Physiol. 2002, 130:1506-1515.
21. Zhao J., et al. Two putative BIN2 substrates are nuclear components of brassinosteroid signaling. Plant Physiol. 2002, 130:1221-1229.
22. He J.X., et al. The GSK3-like kinase BIN2 phosphorylates and destabilizes BZR1, a positive regulator of the brassinosteroid signaling pathway in Arabidopsis. Proc. Natl. Acad. Sci. U.S.A. 2002, 99:10185-10190.
23. Yin Y., et al. BES1 accumulates in the nucleus in response to brassinosteroids to regulate gene expression and promote stem elongation. Cell 2002, 109:181-191.
24. Ingham P.W., et al. Mechanisms and functions of Hedgehog signalling across the metazoa. Nat. Rev. Genet. 2011, 12:393-406.
25. Ryu H., et al. Nucleocytoplasmic shuttling of BZR1 mediated by phosphorylation is essential in Arabidopsis brassinosteroid signaling. Plant Cell 2007, 19:2749-2762.
26. Ryu H., et al. Phosphorylation dependent nucleocytoplasmic shuttling of BES1 is a key regulatory event in brassinosteroid signaling. Mol. Cells 2010, 29:283-290.
27. Ginger R.S., et al. Glycogen synthase kinase-3 enhances nuclear export of a Dictyostelium STAT protein. EMBO J. 2000, 19:5483-5491.
28. Crabtree G.R., Olson E.N. NFAT signaling: choreographing the social lives of cells. Cell 2002, 109(Suppl.):S67-S79.
29. Peng P., et al. A direct docking mechanism for a plant GSK3-like kinase to phosphorylate its substrates. J. Biol. Chem. 2010, 285:24646-24653.
30. Peng P., et al. Regulation of the Arabidopsis GSK3-like kinase BRASSINOSTEROID-INSENSITIVE 2 through proteasome-mediated protein degradation. Mol. Plant 2008, 1:338-346.
31. Kim T.W., et al. Brassinosteroid signal transduction from cell-surface receptor kinases to nuclear transcription factors. Nat. Cell Biol. 2009, 11:1254-1260.
32. Jaillais Y., et al. Tyrosine phosphorylation controls brassinosteroid receptor activation by triggering membrane release of its kinase inhibitor. Genes Dev. 2011, 25:232-237.
33. Lochhead P.A., et al. A chaperone-dependent GSK3beta transitional intermediate mediates activation-loop autophosphorylation. Mol. Cell 2006, 24:627-633.
34. Vert G., Chory J. Downstream nuclear events in brassinosteroid signalling. Nature 2006, 441:96-100.
35. Yan Z., et al. BIN2 functions redundantly with other Arabidopsis GSK3-like kinases to regulate brassinosteroid signaling. Plant Physiol. 2009, 150:710-721.
36. Yoo M.J., et al. Phylogenetic diversification of glycogen synthase kinase 3/SHAGGY-like kinase genes in plants. BMC Plant Biol. 2006, 6:3.
37. Rozhon W., et al. ASKtheta, a group-III Arabidopsis GSK3, functions in the brassinosteroid signalling pathway. Plant J. 2010, 62:215-223.
38. De Rybel B., et al. Chemical inhibition of a subset of Arabidopsis thaliana GSK3-like kinases activates brassinosteroid signaling. Chem. Biol. 2009, 16:594-604.
39. Sun Y., Allen R.D. Functional analysis of the BIN2 genes of cotton. Mol. Genet. Genomics 2005, 274:51-59.
40. Koh S., et al. T-DNA tagged knockout mutation of rice OsGSK1, an orthologue of Arabidopsis BIN2, with enhanced tolerance to various abiotic stresses. Plant Mol. Biol. 2007, 65:453-466.
41. Zhang S., et al. The primary signaling outputs of brassinosteroids are regulated by abscisic acid signaling. Proc. Natl. Acad. Sci. U.S.A. 2009, 106:4543-4548.
42. Vert G., et al. Integration of auxin and brassinosteroid pathways by Auxin Response Factor 2. Proc. Natl. Acad. Sci. U.S.A. 2008, 105:9829-9834.
43. Nemhauser J.L., et al. Interdependency of brassinosteroid and auxin signaling in Arabidopsis. PLoS Biol. 2004, 2:E258.
44. Vanneste S., et al. Cell cycle progression in the pericycle is not sufficient for SOLITARY ROOT/IAA14-mediated lateral root initiation in Arabidopsis thaliana. Plant Cell 2005, 17:3035-3050.
45. Dornelas M.C., et al. Arabidopsis thaliana SHAGGY-related protein kinases (AtSK11 and 12) function in perianth and gynoecium development. Plant J. 2000, 21:419-429.
46. Charrier B., et al. Expression profiling of the whole Arabidopsis shaggy-like kinase multigene family by real-time reverse transcriptase-polymerase chain reaction. Plant Physiol. 2002, 130:577-590.
47. Tavares R., et al. AtSKtheta, a plant homologue of SGG/GSK-3 marks developing tissues in Arabidopsis thaliana. Plant Mol. Biol. 2002, 50:261-271.
48. Claisse G., et al. The Arabidopsis thaliana GSK3/Shaggy like kinase AtSK3-2 modulates floral cell expansion. Plant Mol. Biol. 2007, 64:113-124.
49. Piao H.L., et al. Constitutive over-expression of AtGSK1 induces NaCl stress responses in the absence of NaCl stress and results in enhanced NaCl tolerance in Arabidopsis. Plant J. 2001, 27:305-314.
50. Richard O., et al. Organization and expression of the GSK3/shaggy kinase gene family in the moss Physcomitrella patens suggest early gene multiplication in land plants and an ancestral response to osmotic stress. J. Mol. Evol. 2005, 61:99-113.
51. Kempa S., et al. A plastid-localized glycogen synthase kinase 3 modulates stress tolerance and carbohydrate metabolism. Plant J. 2007, 49:1076-1090.
52. Patade V.Y., et al. Expression analysis of sugarcane shaggy-like kinase (SuSK) gene identified through cDNA subtractive hybridization in sugarcane (Saccharum officinarum L.). Protoplasma 2011, 248:613-621.
53. Chen G.P., et al. Isolation and characterization of TaGSK1 involved in wheat salt tolerance. Plant Sci. 2003, 165:1369-1375.
54. Wrzaczek M., et al. A proteasome-regulated glycogen synthase kinase-3 modulates disease response in plants. J. Biol. Chem. 2007, 282:5249-5255.
55. Jonak C., et al. Wound-induced expression and activation of WIG, a novel glycogen synthase kinase 3. Plant Cell 2000, 12:1467-1475.
56. Xiao Y., Mitchell A.P. Shared roles of yeast glycogen synthase kinase 3 family members in nitrogen-responsive phosphorylation of meiotic regulator Ume6p. Mol. Cell. Biol. 2000, 20:5447-5453.
57. Kassir Y., et al. The Saccharomyces cerevisiae GSK-3 beta homologs. Curr. Drug Targets 2006, 7:1455-1465.
58. Pereira J., et al. Yap4 PKA- and GSK3-dependent phosphorylation affects its stability but not its nuclear localization. Yeast 2009, 26:641-653.
59. Andoh T., et al. Yeast glycogen synthase kinase 3 is involved in protein degradation in cooperation with Bul1, Bul2, and Rsp5. Mol. Cell. Biol. 2000, 20:6712-6720.
60. Piao H.L., et al. An Arabidopsis GSK3/shaggy-like gene that complements yeast salt stress-sensitive mutants is induced by NaCl and abscisic acid. Plant Physiol. 1999, 119:1527-1534.
61. Rensing S.A., et al. The Physcomitrella genome reveals evolutionary insights into the conquest of land by plants. Science 2008, 319:64-69.
62. Banks J.A., et al. The Selaginella genome identifies genetic changes associated with the evolution of vascular plants. Science 2011, 332:960-963.
63. Chono M., et al. A semidwarf phenotype of barley uzu results from a nucleotide substitution in the gene encoding a putative brassinosteroid receptor. Plant Physiol. 2003, 133:1209-1219.
64. Morinaka Y., et al. Morphological alteration caused by brassinosteroid insensitivity increases the biomass and grain production of rice. Plant Physiol. 2006, 141:924-931.
65. Bai M.Y., et al. Functions of OsBZR1 and 14-3-3 proteins in brassinosteroid signaling in rice. Proc. Natl. Acad. Sci. U.S.A. 2007, 104:13839-13844.
66. Salinas P.C. Modulation of the microtubule cytoskeleton: a role for a divergent canonical Wnt pathway. Trends Cell Biol. 2007, 17:333-342.
67. Ong Tone S., et al. GSK3 regulates mitotic chromosomal alignment through CRMP4. PLoS ONE 2010, 5:e14345.
68. Gardiner J., Marc J. Arabidopsis thaliana, a plant model organism for the neuronal microtubule cytoskeleton?. J. Exp. Bot. 2011, 62:89-97.
69. Ainsworth C. Cilia: tails of the unexpected. Nature 2007, 448:638-641.
70. Wilson N.F., Lefebvre P.A. Regulation of flagellar assembly by glycogen synthase kinase 3 in Chlamydomonas reinhardtii. Eukaryot. Cell 2004, 3:1307-1319.