Early action of pea symbiotic gene NOD3 is confirmed by adventitious root phenotype

Plant Science

Volumn 179, Issue 5, 2010, Pages 472-478

  Novák, Karel ^a  

^a INSTITUTE OF MICROBIOLOGY   (Czech Republic)

Author keywords

Grafting; Pisum sativum; Rhizobium; Supernodulation

Indexed keywords

PISUM SATIVUM; RHIZOBIUM;

EID: 77956778680     PISSN: 01689452     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.plantsci.2010.07.007     Document Type: Article

References (60)

1. Willems A. The taxonomy of rhizobia: an overview. Plant Soil 2006, 287:3-14.
2. Spaink H.P. Root nodulation and infection factors produced by rhizobial bacteria. Annu. Rev. Microbiol. 2000, 54:257-288.
3. Radutoiu S., Madsen L.H., Madsen E.B., Felle H.H., Umehara Y., Gronlund M., Sato S., Nakamura Y., Tabata S., Sandal N., Stougaard J. Plant recognition of symbiotic bacteria requires two LysM receptor-like kinases. Nature 2003, 425:585-592.
4. Arrighi J.F., Barré A., Ben Amor B., Bersoult A., Soriano L.C., Mirabella R., De Carvalho-Niebel F., Journet E.-P., Gherardi M., Huguet T., Geurts R., Dénarié J., Rougé P., Gough C. The Medicago truncatula lysine motif-receptor-like kinase gene family includes NFP and new nodule-expressed genes. Plant Physiol. 2006, 142:265-279.
5. Limpens E., Franken C., Smit P., Willemse J., Bisseling T., Geurts R. LysM domain receptor kinases regulating rhizobial Nod factor-induced infection. Science 2003, 302:630-633.
6. Stracke S., Kistner C., Yoshida S., Mulder L., Sato S., Kaneko T., Tabata S., Sandal N., Stougaard J., Szczyglowski K., Parniske M. A plant receptor-like kinase required for both bacterial and fungal symbiosis. Nature 2002, 417:959-962.
7. Endre G., Kereszt A., Kevei Z., Mihacea S., Kalo P., Kiss G.B. A receptor kinase gene regulating symbiotic nodule development. Nature 2002, 417:962-966.
8. Ané J.M., Kiss G.B., Riely B.K., Penmetsa R.V., Oldroyd G.E.D., Ayax C., Lévy J., Debellé F., Baek J.M., Kaló P., Rosenberg C., Roe B.A., Long S.R., Dénarié J., Cook D.R. Medicago truncatula dmi1 required for bacterial and fungal symbioses in legumes. Science 2004, 303:1364-1367.
9. Imaizumi-Anraku H., Takeda N., Charpentier M., Perry J., Miwa H., Umehara Y., Kouchi H., Murakami Y., Mulder L., Vickers K., Pike J., Downie J.A., Wang T., Sato S., Asamizu E., Tabata S., Yoshikawa M., Murooka Y., Wu G.J., Kawaguchi M., Kawasaki S., Parniske M., Hayashi M. Plastid proteins crucial for symbiotic fungal and bacterial entry into plant roots. Nature 2005, 433:527-531.
10. 2+ and calmodulin-dependent protein kinase required for bacterial and fungal symbioses. Science 2004, 303:1361-1364.
11. Smit P., Raedts J., Portyanko V., Debelle F., Gough C., Bisseling T., Geurts R. NSP1 of the GRAS protein family is essential for rhizobial Nod factor-induced transcription. Science 2005, 308:1789-1791.
12. Schauser L., Roussis A., Stiller J., Stougaard J. A plant regulator controlling development of symbiotic root nodules. Nature 1999, 402:191-195.
13. Guinel F.C., Geil R.D. A model for the development of the rhizobial and arbuscular mycorrhizal symbioses in legumes and its use to understand the roles of ethylene in the establishment of these two symbioses. Can. J. Bot. 2002, 80:695-720.
14. Carroll B.J., McNeil D.L., Gresshoff P.M. Isolation and properties of soybean (Glycine max (L.) Merr.) mutants that nodulate in the presence of high nitrate concentrations. Proc. Natl. Acad. Sci. U. S. A. 1985, 82:4162-4166.
15. Jacobsen E., Feenstra W.J. A new pea mutant with efficient nodulation in the presence of nitrate. Plant Sci. Lett. 1984, 33:337-344.
16. Bhatia R. Global impact of induced mutations in plant breeding. Serving Human Needs: Nuclear Technology for Sustainable Development 2001, International Atomic Energy Agency, Vienna.
17. Sagan M., Gresshoff P.M. Developmental mapping of nodulation events in pea (Pisum sativum L.) using supernodulating plant genotypes and bacterial variability reveals both plant and Rhizobium control of nodulation regulation. Plant Sci. 1996, 117:167-179.
18. Li D.X., Kinkema M., Gresshoff P.M. Autoregulation of nodulation (AON) in Pisum sativum (pea) involves signalling events associated with both nodule primordia development and nitrogen fixation. J. Plant Physiol. 2009, 166:955-967.
19. Day D.A., Carroll B.J., Delves A.C., Gresshoff P.M. Relationship between autoregulation and nitrate inhibition of nodulation in soybeans. Physiol. Plant. 1989, 75:37-42.
20. Delves A.C., Higgins A.V., Gresshoff P.M. Shoot control of supernodulation in a number of mutant soybeans, Glycine max (L.) Merr. Aust. J. Plant Physiol. 1987, 14:689-694.
21. Kinkema M., Scott P.T., Gresshoff P.M. Legume nodulation: successful symbiosis through short- and long-distance signalling. Funct. Plant Biol. 2006, 33:707-721.
22. Krusell L., Madsen L.H., Sato S., Aubert G., Genua A., Szczyglowski K., Duc G., Kaneko T., Tabata S., de Bruijn F., Pajuelo E., Sandal N., Stougaard J. Shoot control of root development and nodulation is mediated by a receptor-like kinase. Nature 2002, 420:422-426.
23. Searle I.R., Men A.E., Laniya T.S., Buzas D.M., Iturbe-Ormaetxe I., Carroll B.J., Gresshoff P.M. Long-distance signaling in nodulation directed by a CLAVATA1-like receptor kinase. Science 2003, 299:109-112.
24. Schnabel E., Journet E.P., de Carvalho-Niebel F., Duc G., Frugoli J. The Medicago truncatula SUNN gene encodes a CLV1-like leucine-rich repeat receptor kinase that regulates nodule number and root length. Plant Mol. Biol. 2005, 58:809-822.
25. Oka-Kira E., Kawaguchi M. Long-distance signaling to control root nodule number. Curr. Opin. Plant Biol. 2006, 9:496-502.
26. Sagan M., Duc G. Sym28 and Sym29, two new genes involved in regulation of nodulation in pea (Pisum sativum L.). Symbiosis 1996, 20:229-245.
27. Oelkers K., Goffard N., Weiller G.F., Gresshoff P.M., Mathesius U., Frickey T. Bioinformatic analysis of the CLE signaling peptide family. BMC Plant Biol. 2009, 9:17.
28. Okamoto S., Ohnishi E., Sato S., Takahashi H., Nakazono M., Tabata S., Kawaguchi M. Nod factor/nitrate-induced CLE genes that drive HAR1-mediated systemic regulation of nodulation. Plant Cell Physiol. 2009, 50:67-77.
29. Postma J.G., Jacobsen E., Feenstra W.J. Three pea mutants with an altered nodulation studied by genetic analysis and grafting. J. Plant Physiol. 1998, 132:424-430.
30. Sidorova K.K., Shumnyi V.K. A collection of symbiotic mutants in pea Pisum sativum L.: creation and genetic study. Russ. J. Genet. 2003, 39:406-413.
31. Ishikawa K., Yokota K., Li Y.Y., Wang Y.X., Liu C.T., Suzuki S., Aono T., Oyaizu H. Isolation of a novel root-determined hypernodulation mutant rdh1 of Lotus japonicus. Soil Sci. Plant Nutr. 2008, 54:259-263.
32. Caetano-Anollés G., Gresshoff P.M. Alfalfa controls nodulation during the onset of Rhizobium-induced cortical cell division. Plant Physiol. 1991, 95:366-373.
33. Penmetsa R.V., Uribe P., Anderson J., Lichtenzveig J., Gish J.C., Nam Y.W., Engstrom E., Xu K., Sckisel G., Pereira M., Baek J.M., Lopez-Meyer M., Long S.R., Harrison M.J., Singh K.B., Kiss G.B., Cook D.R. The Medicago truncatula ortholog of Arabidopsis EIN2, sickle, is a negative regulator of symbiotic and pathogenic microbial associations. Plant J. 2008, 55(2008):580-595.
34. Vernié T., Moreau S., De Billy F., Plet J., Combier J.P., Rogers C., Oldroyd G., Frugier F., Niebel A., Gamas P. EFD is an ERF transcription factor involved in the control of nodule number and differentiation in Medicago truncatula. Plant Cell 2008, 20:2696-2713.
35. Novák K., Škrdleta V., Kropáčová M., Lisá L., Němcová M. Interaction of two genes controlling symbiotic nodule number in pea (Pisum sativum L.). Symbiosis 1997, 23:43-62.
36. Penmetsa R.V., Frugoli J.A., Smith L.S., Long S.R., Cook D.R. Dual genetic pathways controlling nodule number in Medicago truncatula. Plant Physiol. 2003, 131:998-1008.
37. Engvild K.C. Nodulation and nitrogen fixation mutants of pea, Pisum sativum. Theor. Appl. Genet. 1987, 74:711-713.
38. Lie T.A. Host genes in Pisum sativum L. conferring resistance to European Rhizobium leguminosarum strains. Plant Soil 1984, 82:415-425.
39. Novák K. Allelic relationships of pea nodulation mutants. J. Hered. 2003, 94:191-193.
40. Josey D.P., Beynon J.L., Johnston A.W.B., Beringer J.E. Strain identification in Rhizobium using intrinsic antibiotic resistance. J. Appl. Bacteriol. 1979, 46:343-350.
41. Škrdleta V., Gaudinová A., Němcová M., Hyndráková A. Symbiotic dinitrogen fixation as affected by short-term application of nitrate to nodulated Pisum sativum L. Folia Microbiol. 1980, 25:155-161.
42. Ellis T.H.N. Approaches to the genetic mapping of pea. Modern Meth. Plant Anal. 1994, 16:117-160.
43. Novák K., Felsberg J., Biedermannová E., Vondrys J. A mutation affecting symbiosis in the pea line Risnod27 changes the ion selectivity filter of the DMI1 homolog. Biol. Plant. 2009, 53:451-460.
44. Molecular Cloning: A Laboratory Manual 1989, Cold Spring Harbor Laboratory Press, Cold Spring Harbor. J. Sambrook, E.F. Fritsch, T. Maniatis (Eds.).
45. Gualtieri G., Kulikova O., Limpens E., Kim D.J., Cook D.R., Bisseling T., Geurts R. Microsynteny between pea and Medicago truncatula in the SYM2 region. Plant Mol. Biol. 2002, 50:225-235.
46. Novák K., Škrdleta V., Němcová M., Lisá L. Symbiotic traits, growth, and classification of pea nodulation mutants. Rostl. Výr. (Plant Production - Prague) 1993, 39:157-170.
47. Novák K., Škrdleta V., Němcová M., Lisá L. Behavior of pea nodulation mutants as affected by increasing nitrate level. Symbiosis 1993, 15:195-206.
48. Gelin O., Blixt S. Root nodulation in peas. Agric. Hortic. Genet. 1964, 22:149-159.
49. Sidorova K.K., Shumny V.K., Vlasova E.Y., Glianenko M.N., Mischenko T.M. Interaction of two symbiotic genes, nod3 and Nod5, in one genotype of pea Pisum sativum L. Dokl. Akad. Nauk 2008, 419:569-571.
50. Novák K., Biedermannová E., Vondrys J. Symbiotic and growth performance of supernodulating forage pea lines. Crop Sci. 2009, 49:1227-1234.
51. Murray J., Karas B., Ross L., Brachmann A., Wagg C., Geil R., Perry J., Nowakowski K., MacGillivary M., Held M., Stougaard J., Peterson L., Parniske M., Szczyglowski K. Genetic suppressors of the Lotus japonicus har1-1 hypernodulation phenotype. Mol. Plant Microbe Interact. 2006, 19:1082-1091.
52. Smýkal P., Horáček J., Dostálová R., Hýbl M. Variety discrimination in pea (Pisum sativum L.) by molecular, biochemical and morphological markers. J. Appl. Genet. 2008, 49:155-166.
53. Kozik A., Heidstra R., Horvath B., Kulikova O., Tikhonovich I., Ellis T.H.N., van Kammen A., Lie T.A., Bisseling T. Pea lines carrying syml or sym2 can be nodulated by Rhizobium strains containing nodX; sym1 and sym2 are allelic. Plant Sci. 1995, 108:41-49.
54. Temnykh S.V., Kneen B.E., Weeden N.F., LaRue T.A. Localization of nod-3, a gene conditioning hypernodulation, and identification of a novel translocation in Pisum sativum L. cv Rondo. J. Hered. 1995, 86:303-305.
55. Temnykh S.V., Weeden N.F., LaRue T.A. Sym-2 and nod-3 are independent but closely linked genes influencing nodule development in pea. Pisum Genet. 1995, 27:26-28.
56. Borisov A.Y., Jacobi L.M., Lebsky V.K., Morzhina E.V., Tsyganov V.E., Voroshilova V.A., Tikhonovich L.A. Genetic system controlling development of nitrogen-fixing nodules and arbuscular mycorrhiza. Pisum Genet. 1999, 31:40-43.
57. Zhukov V., Radutoiu S., Madsen L.H., Rychagova T., Ovchinnikova E., Borisov A., Tikhonovich I., Stougaard J. The pea Sym37 receptor kinase gene controls infection-thread initiation and nodule development. Mol. Plant Microbe Interact. 2008, 21:1600-1608.
58. Cros-Arteil S., Pfaff T., Barker D.G., Journet E.P. Cuttings and grafts. Medicago Truncatula Handbook 2006, http://www.noble.org/MedicagoHandbook/. U. Mathesius, E.P. Journet, L.W. Sumner (Eds.).
59. McComb A.J., McComb J.A. Growth substances and relation between phenotype and genotype in Pisum sativum. Planta 1970, 91:235-345.
60. Somers D.A., Samac D.A., Olhoft P.M. Recent advances in legume transformation. Plant Physiol. 2003, 131:892-899.