publication . Other literature type . Article . 2017

Evolution of strigolactone receptors by gradual neo-functionalization of KAI2 paralogues

Bythell-Douglas, Rohan; Rothfels, Carl J.; Stevenson, Dennis W. D.; Graham, Sean W.; Wong, Gane Ka-Shu; Nelson, David C.; Bennett, Tom;
  • Published: 29 Jun 2017
  • Publisher: University of Alberta Libraries
  • Country: United States
Abstract
Background Strigolactones (SLs) are a class of plant hormones that control many aspects of plant growth. The SL signalling mechanism is homologous to that of karrikins (KARs), smoke-derived compounds that stimulate seed germination. In angiosperms, the SL receptor is an α/β-hydrolase known as DWARF14 (D14); its close homologue, KARRIKIN INSENSITIVE2 (KAI2), functions as a KAR receptor and likely recognizes an uncharacterized, endogenous signal (‘KL’). Previous phylogenetic analyses have suggested that the KAI2 lineage is ancestral in land plants, and that canonical D14-type SL receptors only arose in seed plants; this is paradoxical, however, as non-vascular pla...
Subjects
free text keywords: Lactones, Hydrolases, Plant Growth Regulators, Plant Proteins, Evolution, Molecular, Phylogeny, Signal Transduction, Embryophyta, Charophyceae, Neo-functionalization, Phylogenetics, Strigolactone evolution, Strigolactone signalling, Developmental Biology, Biological Sciences, Evolution, Molecular, Biotechnology, Plant Science, General Biochemistry, Genetics and Molecular Biology, Cell Biology, Physiology, Ecology, Evolution, Behavior and Systematics, Structural Biology, General Agricultural and Biological Sciences, Homology (biology), Strigolactone, Plant evolution, Genetics, Karrikin, Phylogenetic tree, Receptor, Structural variation, Biology, Biology (General), QH301-705.5, Research Article
73 references, page 1 of 5

Al-Babili, S, Bouwmeester, HJ. Strigolactones, a novel carotenoid-derived plant hormone. Annu Rev Plant Biol. 2015; 66: 161-86 [OpenAIRE] [PubMed] [DOI]

López-Ráez, JA, Charnikhova, T, Gómez-Roldán, V, Matusova, R, Kohlen, W, De Vos, R. Tomato strigolactones are derived from carotenoids and their biosynthesis is promoted by phosphate starvation. New Phytol. 2008; 178: 863-74 [OpenAIRE] [PubMed] [DOI]

Borghi, L, Liu, GW, Emonet, A, Kretzschmar, T, Martinoia, E. The importance of strigolactone transport regulation for symbiotic signalling and shoot branching. Planta. 2016; 243: 1351-60 [OpenAIRE] [PubMed] [DOI]

Matthys, C, Walton, A, Struk, S, Stes, E, Boyer, FD, Gevaert, K, Goormachtig, S. The whats, the wheres and the hows of strigolactone action in the roots. Planta. 2016; 243: 1327-37 [OpenAIRE] [PubMed] [DOI]

Kohlen, W, Charnikhova, T, Liu, Q, Bours, R, Domagalska, MA, Beguerie, S. Strigolactones are transported through the xylem and play a key role in shoot architectural response to phosphate deficiency in nonarbuscular mycorrhizal host Arabidopsis. Plant Physiol. 2011; 155: 974-87 [OpenAIRE] [PubMed] [DOI]

Smith, SM, Waters, MT. Strigolactones: destruction-dependent perception?. Curr Biol. 2012; 22: R924-927 [OpenAIRE] [PubMed] [DOI]

Waters, MT, Gutjahr, C, Bennett, T, Nelson, D. Strigolactone signalling and evolution. Ann Rev Plant Biol.. 2017; 68: 8.1-8.31 [OpenAIRE] [DOI]

de Saint, GA, Clavé, G, Badet-Denisot, MA, Pillot, JP, Cornu, D, Le Caer, JP. An histidine covalent receptor and butenolide complex mediates strigolactone perception. Nat Chem Biol. 2016; 12: 787-94 [OpenAIRE] [PubMed] [DOI]

Yao, R, Ming, Z, Yan, L, Li, S, Wang, F, Ma, S. DWARF14 is a non-canonical hormone receptor for strigolactone. Nature. 2016; 536: 469-73 [OpenAIRE] [PubMed] [DOI]

Stirnberg, P, van De Sande, K, Leyser, HM. MAX1 and MAX2 control shoot lateral branching in Arabidopsis. Development. 2002; 129: 1131-41 [PubMed]

Stirnberg, P, Furner, IJ, Leyser, HMO. MAX2 participates in an SCF complex which acts locally at the node to suppress shoot branching. Plant J. 2007; 50: 80-94 [OpenAIRE] [PubMed] [DOI]

Hamiaux, C, Drummond, RS, Janssen, BJ, Ledger, SE, Cooney, JM, Newcomb, RD, Snowden, KC. DAD2 is an alpha/beta hydrolase likely to be involved in the perception of the plant branching hormone, strigolactone. Curr Biol. 2012; 22: 2032-6 [OpenAIRE] [PubMed] [DOI]

Zhao, LH, Zhou, XE, Yi, W, Wu, Z, Liu, Y, Kang, Y. Destabilization of strigolactone receptor DWARF14 by binding of ligand and E3-ligase signalling effector DWARF3. Cell Res. 2015; 25: 1219-36 [OpenAIRE] [PubMed] [DOI]

Nakamura, H, Xue, YL, Miyakawa, T, Hou, F, Qin, HM, Fukui, K. Molecular mechanism of strigolactone perception by DWARF14. Nat Commun. 2013; 4: 2613 [PubMed]

Wang, Y, Sun, S, Zhu, W, Jia, K, Yang, H, Wang, X. Strigolactone/MAX2-induced degradation of brassinosteroid transcriptional effector BES1 regulates shoot branching. Dev Cell. 2013; 27: 681-8 [OpenAIRE] [PubMed] [DOI]

73 references, page 1 of 5
Abstract
Background Strigolactones (SLs) are a class of plant hormones that control many aspects of plant growth. The SL signalling mechanism is homologous to that of karrikins (KARs), smoke-derived compounds that stimulate seed germination. In angiosperms, the SL receptor is an α/β-hydrolase known as DWARF14 (D14); its close homologue, KARRIKIN INSENSITIVE2 (KAI2), functions as a KAR receptor and likely recognizes an uncharacterized, endogenous signal (‘KL’). Previous phylogenetic analyses have suggested that the KAI2 lineage is ancestral in land plants, and that canonical D14-type SL receptors only arose in seed plants; this is paradoxical, however, as non-vascular pla...
Subjects
free text keywords: Lactones, Hydrolases, Plant Growth Regulators, Plant Proteins, Evolution, Molecular, Phylogeny, Signal Transduction, Embryophyta, Charophyceae, Neo-functionalization, Phylogenetics, Strigolactone evolution, Strigolactone signalling, Developmental Biology, Biological Sciences, Evolution, Molecular, Biotechnology, Plant Science, General Biochemistry, Genetics and Molecular Biology, Cell Biology, Physiology, Ecology, Evolution, Behavior and Systematics, Structural Biology, General Agricultural and Biological Sciences, Homology (biology), Strigolactone, Plant evolution, Genetics, Karrikin, Phylogenetic tree, Receptor, Structural variation, Biology, Biology (General), QH301-705.5, Research Article
73 references, page 1 of 5

Al-Babili, S, Bouwmeester, HJ. Strigolactones, a novel carotenoid-derived plant hormone. Annu Rev Plant Biol. 2015; 66: 161-86 [OpenAIRE] [PubMed] [DOI]

López-Ráez, JA, Charnikhova, T, Gómez-Roldán, V, Matusova, R, Kohlen, W, De Vos, R. Tomato strigolactones are derived from carotenoids and their biosynthesis is promoted by phosphate starvation. New Phytol. 2008; 178: 863-74 [OpenAIRE] [PubMed] [DOI]

Borghi, L, Liu, GW, Emonet, A, Kretzschmar, T, Martinoia, E. The importance of strigolactone transport regulation for symbiotic signalling and shoot branching. Planta. 2016; 243: 1351-60 [OpenAIRE] [PubMed] [DOI]

Matthys, C, Walton, A, Struk, S, Stes, E, Boyer, FD, Gevaert, K, Goormachtig, S. The whats, the wheres and the hows of strigolactone action in the roots. Planta. 2016; 243: 1327-37 [OpenAIRE] [PubMed] [DOI]

Kohlen, W, Charnikhova, T, Liu, Q, Bours, R, Domagalska, MA, Beguerie, S. Strigolactones are transported through the xylem and play a key role in shoot architectural response to phosphate deficiency in nonarbuscular mycorrhizal host Arabidopsis. Plant Physiol. 2011; 155: 974-87 [OpenAIRE] [PubMed] [DOI]

Smith, SM, Waters, MT. Strigolactones: destruction-dependent perception?. Curr Biol. 2012; 22: R924-927 [OpenAIRE] [PubMed] [DOI]

Waters, MT, Gutjahr, C, Bennett, T, Nelson, D. Strigolactone signalling and evolution. Ann Rev Plant Biol.. 2017; 68: 8.1-8.31 [OpenAIRE] [DOI]

de Saint, GA, Clavé, G, Badet-Denisot, MA, Pillot, JP, Cornu, D, Le Caer, JP. An histidine covalent receptor and butenolide complex mediates strigolactone perception. Nat Chem Biol. 2016; 12: 787-94 [OpenAIRE] [PubMed] [DOI]

Yao, R, Ming, Z, Yan, L, Li, S, Wang, F, Ma, S. DWARF14 is a non-canonical hormone receptor for strigolactone. Nature. 2016; 536: 469-73 [OpenAIRE] [PubMed] [DOI]

Stirnberg, P, van De Sande, K, Leyser, HM. MAX1 and MAX2 control shoot lateral branching in Arabidopsis. Development. 2002; 129: 1131-41 [PubMed]

Stirnberg, P, Furner, IJ, Leyser, HMO. MAX2 participates in an SCF complex which acts locally at the node to suppress shoot branching. Plant J. 2007; 50: 80-94 [OpenAIRE] [PubMed] [DOI]

Hamiaux, C, Drummond, RS, Janssen, BJ, Ledger, SE, Cooney, JM, Newcomb, RD, Snowden, KC. DAD2 is an alpha/beta hydrolase likely to be involved in the perception of the plant branching hormone, strigolactone. Curr Biol. 2012; 22: 2032-6 [OpenAIRE] [PubMed] [DOI]

Zhao, LH, Zhou, XE, Yi, W, Wu, Z, Liu, Y, Kang, Y. Destabilization of strigolactone receptor DWARF14 by binding of ligand and E3-ligase signalling effector DWARF3. Cell Res. 2015; 25: 1219-36 [OpenAIRE] [PubMed] [DOI]

Nakamura, H, Xue, YL, Miyakawa, T, Hou, F, Qin, HM, Fukui, K. Molecular mechanism of strigolactone perception by DWARF14. Nat Commun. 2013; 4: 2613 [PubMed]

Wang, Y, Sun, S, Zhu, W, Jia, K, Yang, H, Wang, X. Strigolactone/MAX2-induced degradation of brassinosteroid transcriptional effector BES1 regulates shoot branching. Dev Cell. 2013; 27: 681-8 [OpenAIRE] [PubMed] [DOI]

73 references, page 1 of 5
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publication . Other literature type . Article . 2017

Evolution of strigolactone receptors by gradual neo-functionalization of KAI2 paralogues

Bythell-Douglas, Rohan; Rothfels, Carl J.; Stevenson, Dennis W. D.; Graham, Sean W.; Wong, Gane Ka-Shu; Nelson, David C.; Bennett, Tom;