Evolution of the plant-microbe symbiotic 'toolkit'

Trends in Plant Science

Volumn 18, Issue 6, 2013, Pages 298-304

  Delaux, Pierre Marc ^a   Séjalon Delmas, Nathalie ^b   Bécard, Guillaume ^b,c   Ané, Jean Michel ^a  

^a UNIVERSITY OF WISCONSIN MADISON   (United States)

^b UNIVERSITÉ DE TOULOUSE   (France)

^c Centre National de la Recherche Scientifique   (France)

Author keywords

[No Author keywords available]

Indexed keywords

ARBUSCULAR; CHARALES; CHLOROPHYTA; EMBRYOPHYTA; FUNGI; MAGNOLIOPHYTA; RHIZOBIACEAE;

VEGETABLE PROTEIN;

EVOLUTION; GENE REGULATORY NETWORK; GENETICS; METABOLISM; MICROBIOLOGY; MOLECULAR EVOLUTION; MYCORRHIZA; PHYSIOLOGY; PLANT; PLANT PHYSIOLOGY; SYMBIOSIS;

BIOLOGICAL EVOLUTION; EVOLUTION, MOLECULAR; GENE REGULATORY NETWORKS; MYCORRHIZAE; PLANT PHYSIOLOGICAL PHENOMENA; PLANT PROTEINS; PLANTS; SYMBIOSIS;

EID: 84878563088     PISSN: 13601385     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tplants.2013.01.008     Document Type: Review

References (67)

1. Redecker D., et al. Glomalean fungi from the Ordovician. Science 2000, 289:1920-1921.
2. Besserer A., et al. Strigolactones stimulate arbuscular mycorrhizal fungi by activating mitochondria. PLoS Biol. 2006, 4:e226.
3. Maillet F., et al. Fungal lipochitooligosaccharide symbiotic signals in arbuscular mycorrhiza. Nature 2011, 469:58-63.
4. Genre A., et al. Arbuscular mycorrhizal fungi elicit a novel intracellular apparatus in Medicago truncatula root epidermal cells before infection. Plant Cell 2005, 17:3489-3499.
5. Parniske M. Arbuscular mycorrhiza: the mother of plant root endosymbioses. Nat. Rev. Microbiol. 2008, 6:763-775.
6. Gherbi H., et al. SymRK defines a common genetic basis for plant root endosymbioses with arbuscular mycorrhiza fungi, rhizobia, and Frankiabacteria. Proc. Natl. Acad. Sci. U.S.A. 2008, 105:4928-4932.
7. Markmann K., et al. Functional adaptation of a plant receptor-kinase paved the way for the evolution of intracellular root symbioses with bacteria. PLoS Biol. 2008, 6:e68.
8. Wang B., et al. Presence of three mycorrhizal genes in the common ancestor of land plants suggests a key role of mycorrhizas in the colonization of land by plants. New Phytol. 2010, 186:514-525.
9. Delaux P.M., et al. Origin of strigolactones in the green lineage. New Phytol. 2012, 195:857-871.
10. Humphreys C.P., et al. Mutualistic mycorrhiza-like symbiosis in the most ancient group of land plants. Nat. Commun. 2010, 1:103.
11. 2 decline. Nat. Commun. 2012, 3:835.
12. Proust H., et al. Strigolactones regulate protonema branching and act as a quorum sensing-like signal in the moss Physcomitrella patens. Development 2011, 138:1531-1539.
13. Zhang X.C., et al. Evolutionary genomics of LysM genes in land plants. BMC Evol. Biol. 2009, 9:183.
14. Kosuta S., et al. Differential and chaotic calcium signatures in the symbiosis signaling pathway of legumes. Proc. Natl. Acad. Sci. U.S.A. 2008, 105:9823-9828.
15. Engstrom E.M. Phylogenetic analysis of GRAS proteins from moss, lycophyte and vascular plant lineages reveals that GRAS genes arose and underwent substantial diversification in the ancestral lineage common to bryophytes and vascular plants. Plant Signal. Behav. 2011, 6:850-854.
16. Feddermann N., Reinhardt D. Conserved residues in the ankyrin domain of VAPYRIN indicate potential protein-protein interaction surfaces. Plant Signal. Behav. 2011, 6:680-684.
17. Wang E., et al. A common signaling process that promotes mycorrhizal and oomycete colonization of plants. Curr. Biol. 2012, 22:2242-2246.
18. Gobbato E., et al. A GRAS-type transcription factor with a specific function in mycorrhizal signaling. Curr. Biol. 2012, 22:2236-2241.
19. Lauressergues D., et al. The microRNA miR171h modulates arbuscular mycorrhizal colonization of Medicago truncatula by targeting NSP2. Plant J. 2012, 72:512-522.
20. Fonseca H.M., Berbara R.L. Does Lunularia cruciata form symbiotic relationships with either Glomus proliferum or G. intraradices?. Mycol. Res. 2008, 112:1063-1068.
21. Bonfante P., Genre A. Plants and arbuscular mycorrhizal fungi: an evolutionary-developmental perspective. Trends Plant Sci. 2008, 13:492-498.
22. Zhang Y., Guo L.D. Arbuscular mycorrhizal structure and fungi associated with mosses. Mycorrhiza 2007, 17:319-325.
23. Ogura-Tsujita Y., et al. Arbuscular mycorrhiza formation in cordate gametophytes of two ferns, Angiopteris lygodiifolia and Osmunda japonica. J. Plant Res. 2013, 126:41-50.
24. Remy W., et al. Four hundred-million-year-old vesicular arbuscular mycorrhizae. Proc. Natl. Acad. Sci. U.S.A. 1994, 91:11841-11843.
25. Javot H., et al. A Medicago truncatula phosphate transporter indispensable for the arbuscular mycorrhizal symbiosis. Proc. Natl. Acad. Sci. U.S.A. 2007, 104:1720-1725.
26. Nagy R., et al. The characterization of novel mycorrhiza-specific phosphate transporters from Lycopersicon esculentum and Solanum tuberosum uncovers functional redundancy in symbiotic phosphate transport in solanaceous species. Plant J. 2005, 42:236-250.
27. Nagy R., et al. Differential regulation of five Pht1 phosphate transporters from maize (Zea mays L.). Plant Biol. (Stuttg.) 2006, 8:186-197.
28. Paszkowski U., et al. Rice phosphate transporters include an evolutionarily divergent gene specifically activated in arbuscular mycorrhizal symbiosis. Proc. Natl. Acad. Sci. U.S.A. 2002, 99:13324-13329.
29. Rausch C., et al. A phosphate transporter expressed in arbuscule-containing cells in potato. Nature 2001, 414:462-470.
30. Loth-Pereda V., et al. Structure and expression profile of the phosphate Pht1 transporter gene family in mycorrhizal Populus trichocarpa. Plant Physiol. 2011, 156:2141-2154.
31. Ishizaki K., et al. Agrobacterium-mediated transformation of the haploid liverwort Marchantia polymorpha L., an emerging model for plant biology. Plant Cell Physiol. 2008, 49:1084-1091.
32. Smith S., et al. Mycorrhizal Symbiosis 2008, Academic Press. 3rd edn.
33. 2+ spiking in legume nodule development and essential for rhizobial and fungal symbiosis. Proc. Natl. Acad. Sci. U.S.A. 2006, 103:359-364.
34. Saito K., et al. NUCLEOPORIN85 is required for calcium spiking, fungal and bacterial symbioses, and seed production in Lotus japonicus. Plant Cell 2007, 19:610-624.
35. Groth M., et al. NENA, a Lotus japonicus homolog of Sec13, is required for rhizodermal infection by arbuscular mycorrhiza fungi and rhizobia but dispensable for cortical endosymbiotic development. Plant Cell 2010, 22:2509-2526.
36. Ané J.M., et al. Medicago truncatula DMI1 required for bacterial and fungal symbioses in legumes. Science 2004, 303:1364-1367.
37. Waters M.T., et al. The Arabidopsis ortholog of rice DWARF27 acts upstream of MAX1 in the control of plant development by strigolactones. Plant Physiol. 2012, 159:1073-1085.
38. Franzke A., et al. Cabbage family affairs: the evolutionary history of Brassicaceae. Trends Plant Sci. 2011, 16:108-116.
39. Khade S.W., et al. Symbiotic interactions between arbuscular mycorrhizal (AM) fungi and male papaya plants: its status, role and implications. Plant Physiol. Biochem. 2010, 48:893-902.
40. Ming R., et al. The draft genome of the transgenic tropical fruit tree papaya (Carica papaya Linnaeus). Nature 2008, 452:991-996.
41. Tamura K., Hara-Nishimura I. The molecular architecture of the plant nuclear pore complex. J. Exp. Bot. 2012, 10.1093/jxb/ers258.
42. Wiermer M., et al. Putative members of the Arabidopsis Nup107-160 nuclear pore sub-complex contribute to pathogen defense. Plant J. 2012, 70:796-808.
43. Umehara M., et al. Inhibition of shoot branching by new terpenoid plant hormones. Nature 2008, 455:195-200.
44. Gomez-Roldan V., et al. Strigolactone inhibition of shoot branching. Nature 2008, 455:189-194.
45. Kapulnik Y., et al. Strigolactones affect lateral root formation and root-hair elongation in Arabidopsis. Planta 2011, 233:209-216.
46. Liu W., et al. Strigolactone biosynthesis in Medicago truncatula and rice requires the symbiotic GRAS-type transcription factors NSP1 and NSP2. Plant Cell 2011, 23:3853-3865.
47. Lee M.H., et al. Large-scale analysis of the GRAS gene family in Arabidopsis thaliana. Plant Mol. Biol. 2008, 67:659-670.
48. Shahollari B., et al. A leucine-rich repeat protein is required for growth promotion and enhanced seed production mediated by the endophytic fungus Piriformospora indica in Arabidopsis thaliana. Plant J. 2007, 50:1-13.
49. Bulgarelli D., et al. Revealing structure and assembly cues for Arabidopsis root-inhabiting bacterial microbiota. Nature 2012, 488:91-95.
50. Lundberg D.S., et al. Defining the core Arabidopsis thaliana root microbiome. Nature 2012, 488:86-90.
51. Finet C., et al. Multigene phylogeny of the green lineage reveals the origin and diversification of land plants. Curr. Biol. 2010, 20:2217-2222.
52. Wodniok S., et al. Origin of land plants: do conjugating green algae hold the key?. BMC Evol. Biol. 2011, 11:104.
53. Timme R.E., et al. Broad phylogenomic sampling and the sister lineage of land plants. PLoS ONE 2012, 7:e29696.
54. Taylor T.N., et al. Devonian fungi: interactions with the green alga Paleonitella. Mycologia 1992, 84:901-910.
55. Ariosa Y., et al. Epiphytic cyanobacteria on Chara vulgaris are the main contributors to N(2) fixation in rice fields. Appl. Environ. Microbiol. 2004, 70:5391-5397.
56. Abe J., et al. Expression of exogenous genes under the control of endogenous HSP70 and CAB promoters in the Closterium peracerosum-strigosum-littorale complex. Plant Cell Physiol. 2008, 49:625-632.
57. Abe J., et al. Stable nuclear transformation of the Closterium peracerosum-strigosum-littorale complex. Plant Cell Physiol. 2011, 52:1676-1685.
58. Alder A., et al. The path from β-carotene to carlactone, a strigolactone-like plant hormone. Science 2012, 335:1348-1351.
59. Kretzschmar T., et al. A petunia ABC protein controls strigolactone-dependent symbiotic signalling and branching. Nature 2012, 483:341-344.
60. Op den Camp R., et al. LysM-type mycorrhizal receptor recruited for rhizobium symbiosis in nonlegume Parasponia. Science 2011, 331:909-912.
61. Capoen W., et al. Nuclear membranes control symbiotic calcium signaling of legumes. Proc. Natl. Acad. Sci. U.S.A. 2011, 108:14348-14353.
62. 2+ and calmodulin-dependent protein kinase required for bacterial and fungal symbioses. Science 2004, 303:1361-1364.
63. Horváth B., et al. Medicago truncatula IPD3 is a member of the common symbiotic signaling pathway required for rhizobial and mycorrhizal symbioses. Mol. Plant Microbe Interact. 2011, 24:1345-1358.
64. Pumplin N., et al. Medicago truncatula Vapyrin is a novel protein required for arbuscular mycorrhizal symbiosis. Plant J. 2010, 61:482-494.
65. Takeda N., et al. Apoplastic plant subtilases support arbuscular mycorrhiza development in Lotus japonicus. Plant J. 2009, 58:766-777.
66. Zhang Q., et al. Two Medicago truncatula half-ABC transporters are essential for arbuscule development in arbuscular mycorrhizal symbiosis. Plant Cell 2010, 22:1483-1497.
67. Ivanov S., et al. Rhizobium-legume symbiosis shares an exocytotic pathway required for arbuscule formation. Proc. Natl. Acad. Sci. U.S.A. 2012, 109:8316-8321.