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  5. <title>UTas ePrints - Nodulation Phenotypes of Gibberellin and Brassinosteroid Mutants of Peal</title>
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  13. <meta content="Ferguson, Brett J." name="eprints.creators_name" />
  14. <meta content="Ross, John J." name="eprints.creators_name" />
  15. <meta content="Reid, James B." name="eprints.creators_name" />
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  18. <meta content="James.Reid@utas.edu.au" name="eprints.creators_id" />
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  20. <meta content="2007-10-31 02:46:18" name="eprints.datestamp" />
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  23. <meta content="Nodulation Phenotypes of Gibberellin and
  24. Brassinosteroid Mutants of Peal" name="eprints.title" />
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  28. <meta content="The initiation and development of legume nodules induced by compatible Rhizobium species requires a complex signal
  29. exchange involving both plant and bacterial compounds. Phytohormones have been implicated in this process, although in
  30. many cases direct evidence is lacking. Here, we characterize the root and nodulation phenotypes of various mutant lines of pea
  31. (Pisum sativum) that display alterations in their phytohormone levels and/or perception. Mutants possessing root systems
  32. deficient in gibberellins (GAs) or brassinosteroids (BRs) exhibited a reduction in nodule organogenesis. The question of
  33. whether these reductions represent direct or indirect effects of the hormone deficiency is addressed. For example, the
  34. application of GA to the roots of a GA-deficient mutant completely restored its number of nodules to that of the wild type.
  35. Grafting studies revealed that a wild-type shoot or root also restored the nodule number of a GA-deficient mutant. These
  36. findings suggest that GAs are required for nodulation. In contrast, the shoot controlled the number of nodules that formed
  37. in graft combinations of a Bk-deficient mutant and its wild type. The root levels of auxin and GA were similar among
  38. these latter graft combinations. These results suggest that BRs influence a shoot mechanism that controls nodulation and that
  39. the root levels of auxin and GA are not part of this process. Interestingly, a strong correlation between nodule and lateral root
  40. numbers was observed in all lines assessed, consistent with a possible overlap in the early developmental pathways of the two
  41. organs." name="eprints.abstract" />
  42. <meta content="2005" name="eprints.date" />
  43. <meta content="published" name="eprints.date_type" />
  44. <meta content="Plant Physiology" name="eprints.publication" />
  45. <meta content="138" name="eprints.volume" />
  46. <meta content="4" name="eprints.number" />
  47. <meta content="2396-2405" name="eprints.pagerange" />
  48. <meta content="TRUE" name="eprints.refereed" />
  49. <meta content="0032-0889" name="eprints.issn" />
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  51. <meta content="Ait-AliT,SwainSM, ReidJB,SunT-P,KamiyaY(1997)The Lslocusof pea
  52. encodes the gibberellin biosynthesis enzyme ent-kaurene synthase A.
  53. Plant J 11: 443-454 Allen ON, Allen EK (1940) Response of the peanut plant to inoculation with rhizobia, with special reference to morphological development of the nodules. Bot Gaz 102: 121-142 Bao F, Shen J, Brady SR, Muday GK, Asami T, Yang Z (2004) Brassinosteroids
  54. interact with auxin to promote lateral root development
  55. in Arabidopsis. Plant Physiol134: 1624-1631
  56. Plant Physiol. Vol. 138, 2005 2404
  57. Bond L (1948) Origin and developmental morphology of root nodules of Pisum sativum. Bot Gaz 109:411-434
  58. Borisov AY, Barmicheva EM, Jacobi LM, Tsyganov VE, Voroshilova VA,
  59. Tikhonovich IA (2000) Pea (Pisum sativum L.) Mendelian genetics
  60. controlling development of nitrogen-fixing nodules and arbuscular
  61. mycorrhiza. Czech J Gen Plant Breed 36: 106-110
  62. Caetano-Anulles G, Gresshoff PM (1991) Plant genetic control of nodulation.
  63. Annu Rev Microbiol 45: 345-382
  64. Compaan B, Yang WC, Bisseling T, Franssen H (2001) ENOD40 expression
  65. in the pericycle precedes cortical cell division in Rhizobium-legume
  66. interaction and the highly conserved internal region of the gene does not
  67. encode a peptide. Plant Soil 230: 1-8
  68. Dart PJ (1977) Infection and development of leguminous nodules. In
  69. RWF Hardy, ed, A Treatise on Dinitrogen Fixation. Wiley, New York,
  70. pp 367-472
  71. Davidson SE, Elliott RC, Helliwell CA, Poole AT, Reid JB (2003) The pea
  72. gene NA encodes ent-kaurenoic acid oxidase. Plant Physiol131: 335-344
  73. Davidson SE, Smith H, Helliwell CA, Poole AT, Reid JB (2004) The pea
  74. gene LH encodes ent-kaurene oxidase. Plant Physiol134: 1123-1134
  75. Dubrovsky JG, Doerner PW, Coln-Carmona A, Rost TL (2000) Peri cycle
  76. cell proliferation and lateral root initiation in Arabidopsis. Plant Physiol
  77. 124: 1648-1657
  78. Dudley ME, Jacobs TW, Long SL (1987) Microscopic studies of cell divisions
  79. induced in alfalfa roots by Rhizobium meliloti.Planta 171: 289-301
  80. Ferguson BJ, Mathesius U (2003) Signaling interactions during nodule
  81. development. JPlant Growth Regul 22: 47-72
  82. Himanen K, Vuylsteke M, Vanneste S, Vercruysse S, Boucheron E, Alard 1', Chriqui D, Montagu MV, Inze D, Beeckman T (2004) Transcript profiling of early lateral root initiation. Proc Nat! Acad Sci USA 101: 5146-515i
  83. Hirsch AM, LaRue TA (1997) Is the legume nodule a modified root or stem or an organ sui generis? Crit Rev Plant Sci 16:.361-392
  84. Ingram TJ, Reid JB, Murfet IC, Gaskin 1', Willis CL, MacMillan J (1984)
  85. Internode length in Pisum: the Le gene controls the 313-hydroxylation of
  86. gibberellin A20 to gibberellin AI. Planta 83: 1048-1053
  87. Kawaguchi M, Imaizumi-Anraku H, Fukai S, Syono K (1996) Unusual
  88. branching in the seedlings of Lotus japonicus: gibberellins reveal the
  89. nitrogen-sensitive cell divisions within the pericycle on roots. Plant Cell
  90. Physiol 37: 461-470
  91. Lester DR, Ross H, Smith H, Elliott RC, Reid JB (1999) Gibberellin
  92. 2-oxidation and the SLN gene of Pisum sativum. Plant J19: 65-73
  93. Libbenga KR, van Iren F,Bogers RJ, Schraag-Lamers MF (1973) The role of
  94. hormones and gradients in the initiation of cortex proliferation and
  95. nodule formation in Pisum sativum L. Planta 114: 29-39
  96. Lohar DP, Schaff JE, Laskey JG, Kieber H, Bilyeu KD, Bird DM (2004)
  97. Cytokinins play opposite roles in lateral root formation, and nematode
  98. and Rhizobial symbiosis. Plant J38: 203-214
  99. Lorteau M-A, Ferguson BJ, Guinel FC (2001) Effects of cytokinin on
  100. ethylene production and nodulation in pea (Pisum sativum) cv. Sparkle.
  101. Physiol Plant 112: 421-428
  102. Mathesius U (2003) Conservation and divergence of signalling pathways
  103. between roots and soil microbes: the Rhizobium-legume symbiosis
  104. compared to the development of lateral roots, mycorrhizal interactions
  105. and nematode-induced galls. Plant Soil 255: 105-119
  106. McIver J, Djordjevic MA, Weinman H, Rolfe BG (1997) Influence of
  107. Rhizobium leguminosarum biovar trifolii host specific nodulation genes on
  108. the ontogeny of clover nodulation. Protoplasma 172: 166-179
  109. Mylona P, Pawlowski K, Bisseling T (1995) Symbiotic nitrogen fixation.
  110. Plant Cell 7: 869-885 .
  111. Nodulation Phenotypes of Hormone Mutants of Pea
  112. Nomura T, Bishop GJ, Kaneta T, Reid JB, Chory J, Yokota T (2003) The
  113. LKA gene is a BRASSINOSTEROID INSENSITIVE 1 homolog of pea.
  114. Plant J36: 291-300
  115. Nomura T, Jager CE, Kitasaka Y, Takeuchi K, Fukami M, Yoneyama K,
  116. Matsushita Y,Nyunoya H, Takatsuto S, Fujioka S, Smith H, et al (2004)
  117. Brassinosteroid deficiency due to truncated steroid 5a-reductase causes
  118. dwarfism in the lk mutant of pea. Plant Physiol 135: 2220-2229
  119. Nomura T, Kitasaka Y, Takatsuto S, Reid JB, Fukami M, Yokota T (1999)
  120. Brassinosteroid/sterol synthesis and plant growth as affected by lka and
  121. lkb mutations of pea. Plant Physiol119: 1517-1526
  122. NomuraT,NakayamaM,ReidJB, TakeuchiY,Yokota T(1997)Blockageof
  123. brassinosteroid biosynthesis and sensitivity causes dwarfism in garden
  124. pea. Plant Physiol113: 31-37
  125. Nutman PS (1948) Physiological studies on nodule formation. 1. The
  126. relationship between nodulation and lateral root formation in red
  127. clover. Ann Bot (Lond) 12: 81-96
  128. Oldroyd GE, Downie JA (2004) Calcium, kinases and nodulation signalling
  129. in legumes. Nat Rev Mol Cell BioI 5: 566-576
  130. Reid JB (1986) Internode length in Pisum. Three further loci, lh, 15 and lk.
  131. Ann Bot (Lond) 57: 577-592
  132. Reid JB, Murfet IC, Potts WC (1983) Internode length in Pisum. II.
  133. Additional information on the relationship and action of loci Le, La,
  134. Cry, Na and Lm. JExp Bot 34: 349-364
  135. Reid JB, Ross H (1989) Internode length in Pisum. Two further gibberellin
  136. insensitivity genes lka and lkb. Physiol Plant 75: 8~-88
  137. Reid JB, Ross H,Swain SM (1992) Internode length in Pisum: a new, slender
  138. mutant with elevated levels of C19 gibberellins. Planta 188: 462-467
  139. Reid JB, Symons GM, Ross H (2004) Regulation of gibberellin and
  140. brassinosteroid biosynthesis by genetic, environmental and hormonal
  141. factors. In P] Davis, ed, Plant Hormones: Biosynthesis, Signal Transduction,
  142. Action! Kluwer Academic Publishers, Dordrecht, The Netherlands,
  143. pp 179-203
  144. Ross H (1998) Effects of auxin transport inhibitors on gibberellins in pea.
  145. JPlant Growth Regul17: 141-146
  146. Ross H, Reid JB (1986) Internode length in Pisum: the involvement of
  147. ethylene with the gibberellin-insensitive erectoides phenotype. Physiol
  148. Plant 67: 673-679
  149. Ross H, Reid JB, Swain SM (1993) Control of stem elongation by
  150. gibberellin AI: evidence from genetic studies including the slender
  151. mutant, sln. Aust JPlant Physiol 20: 585-599
  152. Russell AJ, Bidartondo MI, Butterfield BG (2002) The root nodules of the
  153. Podocarpaceae harbour arbuscular mycorrhizal fungi. New Phytol 156:
  154. 283-295
  155. Schultz L, Kerckhoffs LHJ, Klahre U, Yokota T, Reid JB (2001) Molecular
  156. characterization of the brassinosteroid-deficient lkb mutant in pea. Plant
  157. Mol BioI 47: 491-498
  158. Symons GM, Reid JB (2004) Brassinosteroids do not undergo longdistance
  159. transport in pea. Implications for the regulation of endogenous
  160. brassinosteroid levels. Plant Physiol 135: 2196-2206
  161. Torrey JG (1976) Initiation and development of root nodules of Casuarina
  162. (Casuarinaceae). Am JBot 63: 335-344
  163. Torrey JG, Callaham D (1978) Determinate development of nodule roots
  164. in actinomycete-induced root nodules of Myrica gale L. Can J Bot 56:
  165. 1357-1364
  166. Wopereis J, Pajuelo E, Dazzo FB, Jiang Q, Gresshoff PM, de Bruijn FJ,
  167. Stougaard J, Szczyglowski K (2000) Short root mutant of Lotus japonicus
  168. with a dramatically altered symbiotic phenotype. Plant J23: 97-114
  169. Yaxley JR, Ross H, Sherriff LJ, Reid JB (2001) Gibberellin biosynthesis
  170. mutations and root development in pea. Plant Physiol 125: 627-633" name="eprints.referencetext" />
  171. <meta content="Ferguson, Brett J. and Ross, John J. and Reid, James B. (2005) Nodulation Phenotypes of Gibberellin and Brassinosteroid Mutants of Peal. Plant Physiology, 138 (4). pp. 2396-2405. ISSN 0032-0889" name="eprints.citation" />
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  174. <meta content="Nodulation Phenotypes of Gibberellin and
  175. Brassinosteroid Mutants of Peal" name="DC.title" />
  176. <meta content="Ferguson, Brett J." name="DC.creator" />
  177. <meta content="Ross, John J." name="DC.creator" />
  178. <meta content="Reid, James B." name="DC.creator" />
  179. <meta content="260000 Earth Sciences" name="DC.subject" />
  180. <meta content="The initiation and development of legume nodules induced by compatible Rhizobium species requires a complex signal
  181. exchange involving both plant and bacterial compounds. Phytohormones have been implicated in this process, although in
  182. many cases direct evidence is lacking. Here, we characterize the root and nodulation phenotypes of various mutant lines of pea
  183. (Pisum sativum) that display alterations in their phytohormone levels and/or perception. Mutants possessing root systems
  184. deficient in gibberellins (GAs) or brassinosteroids (BRs) exhibited a reduction in nodule organogenesis. The question of
  185. whether these reductions represent direct or indirect effects of the hormone deficiency is addressed. For example, the
  186. application of GA to the roots of a GA-deficient mutant completely restored its number of nodules to that of the wild type.
  187. Grafting studies revealed that a wild-type shoot or root also restored the nodule number of a GA-deficient mutant. These
  188. findings suggest that GAs are required for nodulation. In contrast, the shoot controlled the number of nodules that formed
  189. in graft combinations of a Bk-deficient mutant and its wild type. The root levels of auxin and GA were similar among
  190. these latter graft combinations. These results suggest that BRs influence a shoot mechanism that controls nodulation and that
  191. the root levels of auxin and GA are not part of this process. Interestingly, a strong correlation between nodule and lateral root
  192. numbers was observed in all lines assessed, consistent with a possible overlap in the early developmental pathways of the two
  193. organs." name="DC.description" />
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  305. <h1 class="ep_tm_pagetitle">Nodulation Phenotypes of Gibberellin and Brassinosteroid Mutants of Peal</h1>
  306. <p style="margin-bottom: 1em" class="not_ep_block"><span class="person_name">Ferguson, Brett J.</span> and <span class="person_name">Ross, John J.</span> and <span class="person_name">Reid, James B.</span> (2005) <xhtml:em>Nodulation Phenotypes of Gibberellin and Brassinosteroid Mutants of Peal.</xhtml:em> Plant Physiology, 138 (4). pp. 2396-2405. ISSN 0032-0889</p><p style="margin-bottom: 1em" class="not_ep_block"></p><table style="margin-bottom: 1em" class="not_ep_block"><tr><td valign="top" style="text-align:center"><a href="http://eprints.utas.edu.au/2371/1/Nodulation_Phenotypes_of__Gibberellin.pdf"><img alt="[img]" src="http://eprints.utas.edu.au/style/images/fileicons/application_pdf.png" class="ep_doc_icon" border="0" /></a></td><td valign="top"><a href="http://eprints.utas.edu.au/2371/1/Nodulation_Phenotypes_of__Gibberellin.pdf"><span class="ep_document_citation">PDF</span></a> - Full text restricted - Requires a PDF viewer<br />3819Kb</td><td><form method="get" accept-charset="utf-8" action="http://eprints.utas.edu.au/cgi/request_doc"><input accept-charset="utf-8" value="3055" name="docid" type="hidden" /><div class=""><input value="Request a copy" name="_action_null" class="ep_form_action_button" onclick="return EPJS_button_pushed( '_action_null' )" type="submit" /> </div></form></td></tr></table><p style="margin-bottom: 1em" class="not_ep_block">Official URL: <a href="http://proquest.umi.com/pqdweb?did=891347251&amp;sid=1&amp;Fmt=4&amp;clientId=20931&amp;RQT=309&amp;VName=PQD">http://proquest.umi.com/pqdweb?did=891347251&amp;sid=1&amp;Fmt=4&amp;clientId=20931&amp;RQT=309&amp;VName=PQD</a></p><div class="not_ep_block"><h2>Abstract</h2><p style="padding-bottom: 16px; text-align: left; margin: 1em auto 0em auto">The initiation and development of legume nodules induced by compatible Rhizobium species requires a complex signal&#13;
  307. exchange involving both plant and bacterial compounds. Phytohormones have been implicated in this process, although in&#13;
  308. many cases direct evidence is lacking. Here, we characterize the root and nodulation phenotypes of various mutant lines of pea&#13;
  309. (Pisum sativum) that display alterations in their phytohormone levels and/or perception. Mutants possessing root systems&#13;
  310. deficient in gibberellins (GAs) or brassinosteroids (BRs) exhibited a reduction in nodule organogenesis. The question of&#13;
  311. whether these reductions represent direct or indirect effects of the hormone deficiency is addressed. For example, the&#13;
  312. application of GA to the roots of a GA-deficient mutant completely restored its number of nodules to that of the wild type.&#13;
  313. Grafting studies revealed that a wild-type shoot or root also restored the nodule number of a GA-deficient mutant. These&#13;
  314. findings suggest that GAs are required for nodulation. In contrast, the shoot controlled the number of nodules that formed&#13;
  315. in graft combinations of a Bk-deficient mutant and its wild type. The root levels of auxin and GA were similar among&#13;
  316. these latter graft combinations. These results suggest that BRs influence a shoot mechanism that controls nodulation and that&#13;
  317. the root levels of auxin and GA are not part of this process. Interestingly, a strong correlation between nodule and lateral root&#13;
  318. numbers was observed in all lines assessed, consistent with a possible overlap in the early developmental pathways of the two&#13;
  319. organs.</p></div><table style="margin-bottom: 1em" cellpadding="3" class="not_ep_block" border="0"><tr><th valign="top" class="ep_row">Item Type:</th><td valign="top" class="ep_row">Article</td></tr><tr><th valign="top" class="ep_row">Subjects:</th><td valign="top" class="ep_row"><a href="http://eprints.utas.edu.au/view/subjects/260000.html">260000 Earth Sciences</a></td></tr><tr><th valign="top" class="ep_row">ID Code:</th><td valign="top" class="ep_row">2371</td></tr><tr><th valign="top" class="ep_row">Deposited By:</th><td valign="top" class="ep_row"><span class="ep_name_citation"><span class="person_name">Scholarly Publications Librarian</span></span></td></tr><tr><th valign="top" class="ep_row">Deposited On:</th><td valign="top" class="ep_row">31 Oct 2007 13:46</td></tr><tr><th valign="top" class="ep_row">Last Modified:</th><td valign="top" class="ep_row">09 Jan 2008 02:30</td></tr><tr><th valign="top" class="ep_row">ePrint Statistics:</th><td valign="top" class="ep_row"><a target="ePrintStats" href="/es/index.php?action=show_detail_eprint;id=2371;">View statistics for this ePrint</a></td></tr></table><p align="right">Repository Staff Only: <a href="http://eprints.utas.edu.au/cgi/users/home?screen=EPrint::View&amp;eprintid=2371">item control page</a></p>
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