To be or noot to be: Evolutionary tinkering for symbiotic organ identity

Plant Signaling and Behavior

Volumn 8, Issue 8, 2013, Pages

  Couzigou, Jean Malo ^a,b   Mondy, Samuel ^a   Sahl, Lucien ^a   Gourion, Benjamin ^a   Ratet, Pascal ^a  

^a CNRS   (France)

^b Centre National de la Recherche Scientifique   (France)

Author keywords

Auxin; Evolution; Homeosis; Meristem; Organogenesis; Root nodule symbiosis

Indexed keywords

AUXIN; INDOLEACETIC ACID DERIVATIVE; VEGETABLE PROTEIN;

ANTIBODY SPECIFICITY; ARABIDOPSIS; ARTICLE; BARREL MEDIC; EVOLUTION; GENETICS; HOMEOSIS; MERISTEM; METABOLISM; NODULATION; ORGANOGENESIS; PEA; PLANT GENE; ROOT NODULE SYMBIOSIS; SYMBIOSIS;

AUXIN; EVOLUTION; HOMEOSIS; MERISTEM; ORGANOGENESIS; ROOT NODULE SYMBIOSIS;

ARABIDOPSIS; BIOLOGICAL EVOLUTION; GENES, PLANT; INDOLEACETIC ACIDS; MEDICAGO TRUNCATULA; ORGAN SPECIFICITY; PEAS; PLANT PROTEINS; ROOT NODULES, PLANT; SYMBIOSIS;

EID: 84881080838     PISSN: 15592316     EISSN: 15592324     Source Type: Journal    
DOI: 10.4161/psb.24969     Document Type: Article

References (33)

1. Kouchi H, Imaizumi-Anraku H, Hayashi M, Hakoyama T, Nakagawa T, Umehara Y, et al. How many peas in a pod? Legume genes responsible for mutualistic symbioses underground. Plant Cell Physiol. 2010, 51: 1381-1397.PMID:20660226. http://dx.doi.org/10.1093/pcp/pcq107
2. Horváth B, Yeun LH, Domonkos A, Halász G, Gobbato E, Ayaydin F, 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. PMID:21692638. http://dx.doi.org/10.1094/MPMI-01-11-0015
3. Oldroyd GE, Murray JD, Poole PS, Downie JA. The rules of engagement in the legume-rhizobial symbiosis. Annu Rev Genet. 2011. 45:119-144. PMID:21838550. http://dx.doi.org/10.1146/annurev-genet-110410-132549
4. Lauressergues D, Delaux PM, Formey D, Lelandais-Brière C, Fort S, Cottaz S, et al. The microRNA miR171h modulates arbuscular mycorrhizal colonization of Medicago truncatula by targeting NSP2. Plant J. 2012. 72:512-522. PMID:22775306. http://dx.doi.org/10.1111/j.1365-313X.2012.05099.x
5. Gough C, Cullimore J. Lipo-chitooligosaccharide signaling in endosymbiotic plant-microbe interactions. Mol Plant Microbe Interact. 2011. 24:867-878. PMID:21469937. http://dx.doi.org/10.1094/MPMI-01-11-0019
6. Smith ES, Read JD. Mycorrhizal Symbiosis (Academic press). 2008.
7. Delaux PM, Séjalon-Delmas N, Bécard G, Ané JM. Evolution of the plant-microbe symbiotic 'toolkit'. Trends Plant Sci. 2013. In press. PMID:23462549. http://dx.doi.org/10.1016/j.tplants.2013.01.008.
8. Pirozynski KA, Malloch DW. The origin of land plants: a matter of mycotrophism. Biosystems 1975. 6:153-164.PMID:1120179. http://dx.doi.org/10.1016/0303-2647(75)90023-4
9. Wang B, Yeun LH, Xue JY, Liu Y, Ané JM, Qiu YL. 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. PMID:20059702. http://dx.doi.org/10.1111/j.1469-8137.2009.03137.x
10. Soltis DE, Soltis PS, Morgan DR, Swensen SM, Mullin BC, Dowd JM, et al. Chloroplast gene sequence data suggest a single origin of the predisposition for symbiotic nitrogen fixation in angiosperms. Proc Natl Acad Sci USA. 1995. 92:2647-2651. PMID:7708699. http://dx.doi.org/10.1073/pnas.92.7.2647
11. Doyle JJ. Phylogenetic perspectives on the origins of nodulation. Mol Plant Microbe Interact. 2011. 24:1289-1295. PMID:2. 1995796. http://dx.doi.org/10.1094/MPMI-05-11-0114
12. Charpentier M, Oldroyd G. How close are we to nitrogen-fixing cereals? Curr Opin Plant Biol. 2010. 13:556-564. PMID:20817544. http://dx.doi.org/10.1016/j.pbi.2010.08.003
13. Maillet F, Poinsot V, André O, Puech-Pagès V, Haouy A, Gueunier M, et al. Fungal lipochitooligosaccharide symbiotic signals in arbuscular mycorrhiza. Nature. 2011. 469:58-63. PMID:21209659. http://dx.doi.org/10.1038/nature09622
14. Lerouge P, Roche P, Faucher C, Maillet F, Truchet G, Promé JC, et al. Symbiotic host-specificity of Rhizobium meliloti is determined by a sulphated and acylated glucosamine oligosaccharide signal. Nature. 1990. 344:781-784. PMID:2330031. http://dx.doi.org/10.1038/344781a0
15. Tirichine L, Sandal N, Madsen LH, Radutoiu S, Albrektsen AS, Sato S, et al. A gain-of-function mutation in a cytokinin receptor triggers spontaneous root nodule organogenesis. Science. 2007. 315:104-107. PMID:17110537. http://dx.doi.org/10.1126/science.1132397
16. Hirsch AM, Larue TA. Is the legume nodule a modified root or stem or an organ sui generis? Crit Rev Plant Sci. 1997. 16:361-392
17. Gualtieri G, Bisseling T. The evolution of nodulation. Plant Mol Biol. 2000. 42:181-94. PMID:10688136. http://dx.doi.org/10.1023/A:1006396525292.
18. Ferguson BJ, Reid JB. Cochleata: getting to the root of legume nodules. Plant Cell Physiol 2005. 46:1583-1589. PMID:16043431. http://dx.doi.org/10.1093/pcp/pci171
19. Couzigou JM, Zhukov V, Mondy S, Abu el Heba G, Cosson V, Ellis TH, et al. NODULE ROOT and COCHLEATA maintain nodule development and are legume orthologs of Arabidopsis BLADE-ON-PETIOLE genes. Plant Cell. 2012. 24:4498-510. PMID:23136374. http://dx.doi.org/10.1105/tpc.112.103747
20. Dart PJ. Infection and development of leguminous nodules. In: A Treatise on Dinitrogen Fixation Edited by Hardy, RWF Wiley, New York, USA. 1977:367-472.
21. Day JM, Dart PJ. Root formation by legume nodules. Rep Rothamsted Exp Stat 1971. Part I:85.
22. Akasaka Y, Mii M, Daimon H. Morphological alterations and root nodule formation in Agrobacterium rhizogenes-mediated transgenic hairy roots of Peanut (Arachis hypogaea L.). Ann Bot (Lond) 1998. 81:355-62. http://dx.doi.org/10.1006/anbo.1997.0566
23. Sinharoy S, DasGupta M. RNA interference highlights the role of CCaMK in dissemination of endosymbionts in the Aeschynomeneae legume Arachis. Mol Plant Microbe Interact. 2009. 22:1466-1475. PMID:19810815. http://dx.doi.org/10.1094/MPMI-22-11-1466
24. Gourion B, Sulser S, Frunzke J, Francez-Charlot A, Stiefel P, Pessi G, et al. The PhyR-sigma(EcfG) signalling cascade is involved in stress response and symbiotic efficiency in Bradyrhizobium japonicum. Mol Microbiol. 2009. 73:291-305. PMID:19555458.http://dx.doi.org/10.1111/j.1365-2958.2009.06769.x
25. Ferraioli S, Tatè R, Rogato A, Chiurazzi M, Patriarca EJ. Development of ectopic roots from abortive nodule primordia. Mol Plant Microbe Interact 2004. 17:1043-1050. PMID:15497397. http://dx.doi.org/10.1094/MPMI.2004.17.10.1043
26. McIver J, Djordjevic MA, Weinman JJ, Rolfe BG. Influence of Rhizobimn leguminosarum biovar trifolii host specific nodulation genes on the ontogeny of clover nodulation. Protoplasma 1993:166-179. http://dx.doi.org/10.1007/BF01379374
27. Morris AC, Djordjevic MA. The Rhizobium leguminosarum biovar trifolii ANU794 induces novel developmental responses on the subterranean clover cultivar Woogenellup. Mol Plant Microbe Interact. 2006. 19:471-479. PMID:16673934. http://dx.doi.org/10.1094/MPMI-19-0471
28. Norberg M, Holmlund M, Nilsson O. The BLADE ON PETIOLE genes act redundantly to control the growth and development of lateral organs. Development 2005. 132:2203-2213. PMID:15800002. http://dx.doi.org/10.1242/dev.01815
29. Hepworth SR, Zhang Y, McKim S, Li X, Haughn GW. BLADE-ON-PETIOLE-dependent signaling controls leaf and floral patterning in Arabidopsis. Plant Cell 2005. 17:1434-1448. PMID:15805484. http://dx.doi.org/10.1105/tpc.104.030536
30. Osipova M, Dolgikh E, Lutova L. Peculiarities of meristem-specific WOX5 gene expression during nodule organogenesis in legumes. Russ J Dev Biol. 2011. 42:226-237. http://dx.doi.org/10.1134/S1062360411010085
31. Marin E, Jouannet V, Herz A, Lokerse AS, Weijers D, Vaucheret H, et al. miR390, Arabidopsis TAS3 tasiRNAs, and their AUXIN RESPONSE FACTOR targets define an autoregulatory network quantitatively regulating lateral root growth. Plant Cell. 2010. 22:1104-1117. PMID:20363771. http://dx.doi.org/10.1105/tpc.109.072553
32. Barton MK. Twenty years on: the inner workings of the shoot apical meristem, a developmental dynamo. Dev Biol. 2010. 341:95-113. PMID:19961843. http://dx.doi.org/10.1016/j.ydbio.2009.11.029
33. Jacob F. Evolution and tinkering. Science. 1977. 196:1161-1166. PMID:860134. http://dx.doi.org/10.1126/science.860134