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9781405138871

Annual Plant Reviews, Plant Hormone Signaling

by ;
  • ISBN13:

    9781405138871

  • ISBN10:

    1405138874

  • Edition: 1st
  • Format: Hardcover
  • Copyright: 2006-09-01
  • Publisher: Wiley-Blackwell
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Summary

Plant growth is regulated by developmental programmes that can be modified by environmental cues acting through endogenous signalling molecules including plant hormones. This volume provides an overview of the biosynthesis, catabolism, perception and signal transduction of the individual hormone classes, followed by chapters on hormone distribution and transport, and the roles of hormone signalling in specific developmental processes. Particular attention is paid to the regulation of hormone signalling by environmental and developmental cues, sites of hormone metabolism and action, and interactions between hormone signalling pathways. The book is directed at researchers and professionals in plant biochemistry and molecular biology.

Author Biography

Professor Peter Hedden and Dr Stephen Thomas, both Crop Performance and Improvement Division, Rothamsted Research, Harpenden, UK.

Table of Contents

Contributors xiii
Preface xv
1 Abscisic acid synthesis, metabolism and signal transduction
1(36)
ANNIE MARION-POLL and JEFFREY LEUNG
1.1 Introduction
1(1)
1.2 Biosynthesis and catabolism pathways
2(5)
1.2.1 Main early steps of ABA biosynthesis
2(2)
1.2.2 Epoxy-carotenoid cleavage
4(2)
1.2.3 The conversion of xanthoxin to ABA
6(1)
1.2.4 ABA catabolism
6(1)
1.3 Regulation of ABA synthesis and metabolism
7(5)
1.3.1 Developmental regulation
7(1)
1.3.1.1 Vegetative tissues
7(1)
1.3.1.2 Reproductive organs
8(1)
1.3.2 Regulation in response to abiotic stresses
9(1)
1.3.3 Regulation by endogenous signals and factors
10(2)
1.4 ABA signaling in seed maturation processes: proteolysis and combinatorial protein interactions
12(3)
1.5 Stress responses in vegetative tissues: the five major nexuses
15(7)
1.5.1 ABA recognition sites and the search for the receptors
15(2)
1.5.2 Transcriptional network as the readout
17(1)
1.5.3 RNA metabolism
17(2)
1.5.4 Protein phosphatases 2C
19(1)
1.5.5 Sucrose non-fermenting-related kinases
19(3)
1.6 ABA signaling in guard cells: simple movements controlled by complex mechanisms
22(1)
1.7 ABA as antagonizing signal to light in stomatal movement
23(1)
1.8 Concluding remarks
24(1)
Acknowledgements
25(1)
References
26(11)
2 Auxin metabolism and signaling
37(30)
JERRY D. COHEN and WILLIAM M. GRAY
2.1 Introduction
37(1)
2.2 Auxin metabolism
37(9)
2.2.1 Indole-3-acetic acid biosynthesis
37(1)
2.2.1.1 The tryptophan-independent pathway
37(1)
2.2.1.2 IAA biosynthesis from tryptophan
40(2)
2.2.2 IAA conjugates in plants
42(1)
2.2.2.1 IAA-peptide conjugates
42(1)
2.2.2.2 Amino acid conjugates
43(1)
2.2.2.3 Amide conjugate hydrolysis
43(1)
2.2.2.4 Ester conjugates
44(2)
2.2.3 IAA degradation
46(1)
2.3 Auxin signaling
46(12)
2.3.1 Auxin-responsive genes
46(1)
2.3.2 Auxin response factors
47(4)
2.3.3 Regulation of auxin response by the SCFTIR1 ubiquitin–ligase
51(2)
2.3.4 Regulation of SCFTIR1 activity
53(2)
2.3.5 Identification of an auxin receptor
55(3)
2.4 Conclusions and future perspectives
58(1)
Acknowledgements
59(1)
References
59(8)
3 Integration of brassinosteroid biosynthesis and signaling
67(26)
MIKLOS SZEKERES and GERARD J. BISHOP
3.1 Introduction
67(1)
3.2 Metabolism
67(13)
3.2.1 Biosynthesis
67(1)
3.2.1.1 DET2
69(1)
3.2.1.2 SAX I
72(1)
3.2.1.3 DWF4
72(1)
3.2.1.4 CPD
73(1)
3.2.1.5 ROT3 and CYP9ODJ
73(1)
3.2.1.6 CYP85A1 and CYP85A2
74(1)
3.2.1.7 Other biosynthetic functions
74(1)
3.2.2 Inactivation
75(1)
3.2.2.1 BAST
75(1)
3.2.2.2 CHI2/SHK1/SOB7
76(1)
3.2.2.3 UGT73C5
77(1)
3.2.2.4 BNST3 and BNST4
77(1)
3.2.3 Functional aspects of BR metabolism
77(1)
3.2.3.1 Regulation of biosynthetic genes
77(1)
3.2.3.2 Regulation of BR-inactivating genes
78(1)
3.2.3.3 Conservation of BR synthesis in higher plants
79(1)
3.3 Signal transduction
80(4)
3.3.1 BRI1 and BAK1
80(1)
3.3.2 BIN2 and BSU1
81(1)
3.3.3 BZR1 and BZR2/BES1
82(1)
3.3.4 BIM1
82(1)
3.3.5 Signaling mechanism and other putative components
83(1)
3.4 Future prospectives
84(3)
3.4.1 Metabolism
84(2)
3.4.2 Signal transduction
86(1)
3.4.3 Crops
86(1)
Acknowledgements
87(1)
References
87(6)
4 Cytokinin metabolism and signal transduction
93(32)
ALEXANDER HEYL, TOMÁS WERNER and THOMAS SCHMÜLLING
4.1 Introduction
93(1)
4.2 Cytokinin metabolism
93(8)
4.2.1 Cytokinin biosynthesis
94(3)
4.2.2 Cytokinin interconversion and conjugation
97(1)
4.2.3 Cytokinin catabolism
98(3)
4.3 Cytokinin signal transduction
101(16)
4.3.1 Cytokinin signal perception
101(4)
4.3.2 Cytokinin signal transduction
105(12)
4.4 Conclusions
117(1)
References
118(7)
5 Ethylene biosynthesis and signaling: a puzzle yet to be completed
125(22)
FILIP VANDENBUSSCHE, WIM H. VRIEZEN and DOMINIQUE VAN DER STRAETEN
5.1 Introduction
125(1)
5.2 Ethylene biosynthesis
126(5)
5.2.1 ACC synthase
127(3)
5.2.2 ACC oxidase
130(1)
5.3 Ethylene signal transduction
131(6)
5.4 A complex network
137(2)
Acknowledgements
139(1)
References
139(8)
6 Gibberellin metabolism and signal transduction
147(38)
STEPHEN G. THOMAS and PETER HEDDEN
6.1 Introduction
147(1)
6.2 The gibberellin metabolic pathway
148(3)
6.2.1 Biosynthesis of bioactive GAs
148(2)
6.2.2 GA deactivation
150(1)
6.3 Genes of GA biosynthesis and their regulation
151(6)
6.3.1 Developmental regulation
151(3)
6.3.2 Hormonal regulation
154(1)
6.3.3 Environmental regulation
154(3)
6.4 The gibberellin signal transduction pathway
157(9)
6.4.1 The gibberellin receptor
159(1)
6.4.2 DELLA proteins act as repressors of GA signaling
159(2)
6.4.3 GAs promote rapid degradation of DELLA proteins
161(1)
6.4.4 SCFSLY/GID-mediated degradation of DELLA proteins
162(2)
6.4.5 The role of GID1 in DELLA degradation
164(1)
6.4.6 Additional GA-signaling components
164(1)
6.4.6.1 A role for O-linked N-acetylglucosamine transferases in GA signaling
164(1)
6.4.6.2 DWARF1 and PHOR1, possible positive regulators of GA signaling
165(1)
6.5 Downstream transcriptional events induced by GAs
166(4)
6.5.1 GAMYBs
167(2)
6.5.2 Homoeostatic regulation of GA metabolism
169(1)
6.6 Sites of GA signaling
170(4)
6.6.1 Germinating seeds
170(1)
6.6.2 Stems
171(1)
6.6.3 Flower initiation and development
171(1)
6.6.4 The Arabidopsis root
172(2)
6.7 Conclusions
174(2)
Acknowledgements
176(1)
References
176(9)
7 Oxylipins: biosynthesis, signal transduction and action
185(44)
CLAUS WASTERNACK
7.1 Introduction
185(2)
7.2 α-Dioxygenase, phytoprostanes and electrophile compounds
187(2)
7.2.1 α-Dioxygenase
187(1)
7.2.2 Phytoprostanes and electrophile compounds
187(2)
7.3 The LOX pathway
189(10)
7.3.1 The LOX
190(1)
7.3.2 HPOT/HPOD: the branch point in the LOX pathway
191(1)
7.3.3 The AOS branch: jasmonate biosynthesis
192(1)
7.3.3.1 The AOS
192(1)
7.3.3.2 The allene oxide cyclase
193(1)
7.3.3.3 OPR3
194(1)
7.3.3.4 β-oxidation in JA biosynthesis
194(1)
7.3.3.5 Jasmonate metabolites
197(2)
7.4 Mutants in JA biosynthesis and in JA signaling
199(6)
7.4.1 Mutants in JA biosynthesis
199(2)
7.4.2 Mutants in JA signaling
201(2)
7.4.3 Proteasome-mediated JA signaling
203(2)
7.5 JA, OPDA and related compounds in plant-defense reactions
205(8)
7.5.1 Plant-microbe interactions
205(1)
7.5.1.1 Symbiontic interactions
205(1)
7.5.1.2 Plant pathogen interactions
206(1)
7.5.1.3 Cross-talk between JA, SA, ethylene and ABA
207(1)
7.5.2 The wound-response pathway
208(3)
7.5.3 Direct and indirect defense
211(2)
7.6 JA in development
213(3)
7.6.1 Seedling development and root growth
213(1)
7.6.2 Tuber formation
214(1)
7.6.3 Flower formation
214(1)
7.6.4 Senescence
215(1)
7.7 Concluding remarks
216(1)
Acknowledgements
217(1)
References
217(12)
8 Salicylic acid
229(28)
CHRISTOPHE GARCION and JEAN-PIERRE MÉTRAUX
8.1 Introduction
229(1)
8.2 Biosynthesis and metabolism of SA
230(7)
8.2.1 SA biosynthesis via the phenylpropanoid pathway
230(3)
8.2.2 SA biosynthesis through the isochorismate pathway
233(1)
8.2.3 Relative contribution of the isochorismate and BA pathway
234(1)
8.2.4 Regulation and localization of SA biosynthesis
234(1)
8.2.5 Metabolism of SA
235(1)
8.2.6 Biosynthesis of MeSA
236(1)
8.3 Signal transduction and mode of action
237(10)
8.3.1 SA-binding sites
238(1)
8.3.2 SA and signal transduction mediated by MAP kinases
239(1)
8.3.3 SA and the central role of NPR1
240(3)
8.3.4 SA and other regulatory proteins
243(1)
8.3.5 SA and the mobile signal
243(1)
8.3.6 SA and global gene expression
244(2)
8.3.7 SA and virus resistance
246(1)
8.4 Conclusions
247(10)
References
257(1)
9 Hormone distribution and transport 257(36)
JOHN J. ROSS, GREGORY M. SYMONS, LINDY ABAS, JAMES B. REID and CHRISTIAN LUSCHNIG
9.1 Concepts and definitions
257(1)
9.2 Auxins: distribution and transport
257(3)
9.2.1 Auxin distribution: old views and new developments
257(1)
9.2.2 Auxin biosynthesis: not restricted to the shoot anymore
258(2)
9.3 Auxin transport
260(9)
9.3.1 Mass-flow-dependent distribution of auxin
260(1)
9.3.2 Polar auxin transport
260(1)
9.3.2.1 Physiological aspects
260(1)
9.3.2.2 Auxin transporters
263(1)
9.3.2.3 Regulation of the carriers
265(4)
9.3.3 Conclusion: a joint effort required for auxin transport?
269(1)
9.4 GAs: distribution and transport
269(8)
9.4.1 Seeds and fruits
270(1)
9.4.2 Vegetative tissues
270(1)
9.4.2.1 Grafting studies
270(1)
9.4.2.2 Can mature shoot tissue synthesise GAs?
272(1)
9.4.2.3 Monocotyledonous species
274(3)
9.4.3 Conclusion: some GAs can undergo long-distance transport, at least in some circumstances
277(1)
9.5 BRs: distribution and transport
277(6)
9.5.1 BR distribution
278(1)
9.5.2 BR transport
278(1)
9.5.2.1 Exogenous BRs
278(1)
9.5.2.2 Endogenous BRs: grafting studies
279(1)
9.5.2.3 BR transport within the shoot?
281(1)
9.5.2.4 "Short-distance" BR transport?
282(1)
9.5.3 Conclusion: endogenous BRs do not undergo long-distance transport
283(1)
9.6 General discussion
283(1)
Acknowledgements
284(1)
References
284(9)
10 Reproductive development 293(18)
MIGUEL A. BLÁZQUEZ and JOSÉ LEÓN
10.1 Introduction
293(1)
10.2 Flowering time
293(4)
10.2.1 Gibberellins
294(1)
10.2.2 Brassinosteroids
295(1)
10.2.3 Auxins, cytokinins and ethylene
295(1)
10.2.4 Abscisic acid
296(1)
10.2.5 Salicylic acid and the stress-activated transition to flowering
296(1)
10.3 Flower development
297(2)
10.4 Early fruit development
299(3)
10.4.1 Gibberellins
299(1)
10.4.2 Auxin
300(1)
10.4.3 Polyamines
301(1)
10.5 Fruit maturation
302(2)
10.5.1 Ethylene
302(1)
10.5.2 Auxin
303(1)
10.5.3 BRs and ABA
303(1)
10.5.4 Salicylic acid
304(1)
10.6 Conclusions
304(1)
References
304(7)
11 Seed development and germination 311(28)
SHINJIRO YAMAGUCHI and EIJI NAMBARA
11.1 Introduction
311(1)
11.2 Hormonal control of seed development
311(8)
11.2.1 Developmental and physiological phases in seed development
312(1)
11.2.2 Developmental regulators for seed development
313(3)
11.2.3 Regulators of ABA responses in the seed
316(1)
11.2.4 ABA and GA metabolism genes during seed development
317(1)
11.2.5 Regulation of balancing ABA and GA levels during seed development
318(1)
11.2.6 Regulation of ABA and GA action during seed development
319(1)
11.3 Hormonal control of seed germination and post-germinative growth
319(12)
11.3.1 Regulation of GA levels in imbibed seeds
319(1)
11.3.1.1 Light-regulation of GA biosynthesis
320(1)
11.3.1.2 Temperature-regulation of GA biosynthesis
321(1)
11.3.1.3 GA response components in germinating seeds
322(1)
11.3.2 Regulation of ABA levels in imbibed seeds
323(1)
11.3.2.1 De novo ABA biosynthesis and catabolism are involved in regulation of ABA levels
323(1)
11.3.2.2 Light, high temperature, and GA regulation of ABA metabolism
323(1)
11.3.3 Sites of GA biosynthesis and response in imbibed seeds
324(3)
11.3.4 GA and ABA action in the cereal aleurone
327(1)
11.3.4.1 GA and ABA perception
327(1)
11.3.4.2 Crosstalk between GA and ABA action
328(1)
11.3.5 Other hormones: actions of ethylene and brassinosteroids during seed germination
329(1)
11.3.5.1 Ethylene
329(1)
11.3.5.2 Brassinosteroids
330(1)
11.4 Conclusions and perspectives
331(1)
References
331(8)
Index 339

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