Abstract
Studying evolutionarily primitive organisms with simpler genomes can provide information about the core genetic machinery required for any biological process, including hormone production and perception. In this chapter, we present findings on strigolactone biology based on work with two model byrophytes, the moss Physcomitrella patens and the liverwort Marchantia polymorpha. We summarise the existing knowledge of strigolactone biosynthesis in primitive plants, and discuss the role of strigolactones in regulating growth in response to competition from neighbouring plants. We then turn to strigolactone perception and signal transduction, with a focus on the diversity among putative strigolactone receptors in the KAI2/DWARF14 family of α/β-hydrolases. We speculate on the “original” role for strigolactones for early land plants as a rhizosphere signal, before they were adopted as hormones to regulate development. Finally, we summarise discoveries that explain how strigolactones released by plant roots came to be exploited as germination signals by root-parasitic weeds.
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References
Arite T, Umehara M, Ishikawa S, Hanada A, Maekawa M, Yamaguchi S, Kyozuka J (2009) d14, a strigolactone-insensitive mutant of rice, shows an accelerated outgrowth of tillers. Plant Cell Physiol 50:1416–1424
Bowman JL, Kohchi T, Yamato KT et al (2017) Insights into land plant evolution garnered from the Marchantia polymorpha genome. Cell 171:287–304.e15
Bythell-Douglas R, Rothfels CJ, Stevenson DWD, Graham SW, Wong GK-S, Nelson DC, Bennett T (2017) Evolution of strigolactone receptors by gradual neo-functionalization of KAI2 paralogues. BMC Biol 15:52
Challis RJ, Hepworth J, Mouchel C, Waites R, Leyser O (2013) A role for MORE AXILLARY GROWTH1 (MAX1) in evolutionary diversity in strigolactone signaling upstream of MAX2. Plant Physiol 161:1885–1902
Conn CE, Bythell-Douglas R, Neumann D et al (2015) Convergent evolution of strigolactone perception enabled host detection in parasitic plants. Science 349:540–543
Delaux P-M, Xie X, Timme RE et al (2012) Origin of strigolactones in the green lineage. New Phytol 195:857–871
Gutjahr C, Gobbato E, Choi J et al (2015) Rice perception of symbiotic arbuscular mycorrhizal fungi requires the karrikin receptor complex. Science 350:1521–1524
Jiang L, Liu X, Xiong G et al (2013) DWARF 53 acts as a repressor of strigolactone signalling in rice. Nature 504:401–405
Lopez-Obando M, de Villiers R, Hoffmann B et al (2018) Physcomitrella patens MAX2 characterization suggests an ancient role for this F-box protein in photomorphogenesis rather than strigolactone signalling. New Phytol 435:824
Nelson DC, Scaffidi A, Dun EA, Waters MT, Flematti GR, Dixon KW, Beveridge CA, Ghisalberti EL, Smith SM (2011) F-box protein MAX2 has dual roles in karrikin and strigolactone signaling in Arabidopsis thaliana. Proc Natl Acad Sci U S A 108:8897–8902
Proust H, Hoffmann B, Xie X, Yoneyama K, Schaefer DG, Yoneyama K, Nogué F, Rameau C (2011) Strigolactones regulate protonema branching and act as a quorum sensing-like signal in the moss Physcomitrella patens. Development 138:1531–1539
Scaffidi A, Waters MT, Sun YK, Skelton BW, Dixon KW, Ghisalberti EL, Flematti GR, Smith SM (2014) Strigolactone hormones and their stereoisomers signal through two related receptor proteins to induce different physiological responses in Arabidopsis. Plant Physiol 165:1221–1232
Shen H, Zhu L, Bu Q-Y, Huq E (2012) MAX2 affects multiple hormones to promote photomorphogenesis. Mol Plant 5:224–236
Soundappan I, Bennett T, Morffy N, Liang Y, Stanga JP, Abbas A, Leyser O, Nelson DC (2015) SMAX1-LIKE/D53 family members enable distinct MAX2-dependent responses to Strigolactones and Karrikins in Arabidopsis. Plant Cell 27:3143–3159
Toh S, Holbrook-Smith D, Stogios PJ, Onopriyenko O, Lumba S, Tsuchiya Y, Savchenko A, McCourt P (2015) Structure-function analysis identifies highly sensitive strigolactone receptors in Striga. Science 350:203–207
Walker C, Bennett T (2017) Reassessing the evolution of strigolactone synthesis and signalling, biorxiv.org. https://www.biorxiv.org/content/biorxiv/early/2017/12/03/228320.full.pdf. Accessed 30 Jan 2018
Wang L, Wang B, Jiang L et al (2015) Strigolactone signaling in arabidopsis regulates shoot development by targeting D53-Like SMXL repressor proteins for ubiquitination and degradation. Plant Cell 27:3128–3142
Waters MT, Nelson DC, Scaffidi A, Flematti GR, Sun YK, Dixon KW, Smith SM (2012) Specialisation within the DWARF14 protein family confers distinct responses to karrikins and strigolactones in Arabidopsis. Development 139:1285–1295
Waters MT, Gutjahr C, Bennett T, Nelson DC (2017) Strigolactone signaling and evolution. Annu Rev Plant Biol 68:291–322
Xu Y, Miyakawa T, Nosaki S et al (2018) Structural analysis of HTL and D14 proteins reveals the basis for ligand selectivity in Striga. Nat Commun 9:3947
Yoneyama K, Mori N, Sato T et al (2018a) Conversion of carlactone to carlactonoic acid is a conserved function of MAX1 homologs in strigolactone biosynthesis. New Phytol 111:18084
Yoneyama K, Xie X, Yoneyama K, Kisugi T, Nomura T, Nakatani Y, Akiyama K, McErlean CSP (2018b) Which are the major players, canonical or non-canonical strigolactones? J Exp Bot 111:18084
Zhou F, Lin Q, Zhu L et al (2013) D14-SCFD3-dependent degradation of D53 regulates strigolactone signalling. Nature 504:406–410
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Glossary
- Bryophytes
-
an informal, paraphyletic group of non-vascular land plants that includes the liverworts, mosses, and hornworts.
- Embryophytes
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all terrestrial plants (including those that are secondarily aquatic), a group that emerged within the streptophytes.
- Homologue
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a gene copy related by descent to another gene copy. Such a relationship is inferred on the basis of sequence similarity. A gene may have homologues within a species or between species or both. Homologues may be orthologues or paralogues.
- Lycophytes
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one of the earliest groups of tracheophytes that have microphyllous leaves (small leaves with a single vein).
- Monilophytes
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the true ferns with megaphyllous leaves (large leaves with multiple, branched veins).
- Neofunctionalisation
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after gene duplication to produce two paralogues, an evolutionary process whereby one paralogue undergoes mutation to create a new function that was not present in the ancestral gene, allowing the second gene copy to retain the original function. In contrast with subfunctionalisation.
- Orthologue
-
a gene copy that is separated from related sequence by a speciation event. That is, a gene in species A is more closely related to a gene in species B than it is to another gene in species A. The two orthologues arose from a gene duplication event that predated the speciation of A and B. Orthologues often have similar functions in both species.
- Paralogue
-
a gene copy that is not separated from a related sequence by a speciation event. That is, two genes in species A are more closely related to one another than they are to similar sequences in species B. Paralogues arise through a gene duplication event that happened recently within one or both species A and B but after they speciated. Paralogues may indicate that there is functional redundancy or, given enough evolutionary time and selection pressure, functional specialisation.
- Seed plants
-
also known as spermatophytes. Plants that bear seeds, namely, angiosperms (flowering plants) and gymnosperms (conifers and allies).
- Streptophytes
-
the collection of all land plants and the immediate sister group to land plants, namely, the charophyte algae.
- Subfunctionalisation
-
after gene duplication, an evolutionary process whereby each paralogue adopts a different function from each other, when both functions were previously performed by the single ancestral gene. Thus, each paralogue has now become specialised in function from a more generalist ancestor.
- Tracheophytes
-
vascular plants, which conduct water from the roots along vascular strands or tracheids.
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Bonhomme, S., Waters, M. (2019). Evolution of Strigolactone Biosynthesis and Signalling. In: Koltai, H., Prandi, C. (eds) Strigolactones - Biology and Applications. Springer, Cham. https://doi.org/10.1007/978-3-030-12153-2_5
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DOI: https://doi.org/10.1007/978-3-030-12153-2_5
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