Related Content
Search Google Scholar for:
|
|
Science 16 November 1990: Vol. 250. no. 4983, pp. 948 - 954 DOI: 10.1126/science.250.4983.948
|
|
Articles
Developmental Biology of a Plant-Prokaryote Symbiosis: The Legume Root Nodule
Jan-Peter Nap 1 and
Ton Bisseling 2
1 Department of Molecular Biology, Agricultural University, Dreijenlaan 3, 6703 HA Wageningen, The Netherlands
2 Centre for Plant Breeding Research CPO, P.O. Box 16, 6700 AA Wageningen, The Netherlands
The development of nitrogen fixing root nodules on the roots of leguminous plants is induced by soil bacteria (for example, from the genus Rhizobium). The formation of this plant organ involves specific activation of genes in both plant and bacterium. Analysis of these genes gives insight into the way in which plant and bacterium succeed in coordinating plant development.
THIS ARTICLE HAS BEEN CITED BY OTHER ARTICLES:
- Thirteen nodule-specific or nodule-enhanced genes encoding products homologous to cysteine cluster proteins or plant lipid transfer proteins are identified in Astragalus sinicus L. by suppressive subtractive hybridization.
- M.-X. Chou, X.-Y. Wei, D.-S. Chen, and J.-C. Zhou (2006)
J. Exp. Bot.
57, 2673-2685
| Abstract »
| Full Text »
| PDF »
- RNAi Knock-Down of ENOD40s Leads to Significant Suppression of Nodule Formation in Lotus japonicus.
- H. Kumagai, E. Kinoshita, R. W. Ridge, and H. Kouchi (2006)
Plant Cell Physiol.
47, 1102-1111
| Abstract »
| Full Text »
| PDF »
- The White Clover enod40 Gene Family. Expression Patterns of Two Types of Genes Indicate a Role in Vascular Function.
- E. Varkonyi-Gasic and D. W. R. White (2002)
Plant Physiology
129, 1107-1118
| Abstract »
| Full Text »
| PDF »
- Key Role of Bacterial NH4+ Metabolism in Rhizobium-Plant Symbiosis.
- E. J. Patriarca, R. Tate, and M. Iaccarino (2002)
Microbiol. Mol. Biol. Rev.
66, 203-222
| Abstract »
| Full Text »
| PDF »
- The Involvement of a Cysteine Proteinase in the Nodule Development in Chinese Milk Vetch Infected with Mesorhizobium huakuii subsp. rengei.
- Y. Naito, M. Fujie, S. Usami, Y. Murooka, and T. Yamada (2000)
Plant Physiology
124, 1087-1096
| Abstract »
| Full Text »
- Refined analysis of early symbiotic steps of the Rhizobium-Medicago interaction in relationship with microtubular cytoskeleton rearrangements.
- A. Timmers, M. Auriac, and G Truchet (1999)
Development
126, 3617-3628
| Abstract »
| PDF »
- Nodule Parenchyma–Specific Expression of the Sesbania rostrata Early Nodulin Gene SrEnod2 Is Mediated by Its 3' Untranslated Region.
- R. Chen, D. L. Silver, and F. J. de Bruijn (1998)
PLANT CELL
10, 1585-1602
| Abstract »
| Full Text »
- MsPG3, a Medicago sativa polygalacturonase gene expressed during the alfalfa-Rhizobium meliloti interaction.
- J. A. Munoz, C. Coronado, J. Perez-Hormaeche, A. Kondorosi, P. Ratet, and A. J. Palomares (1998)
PNAS
95, 9687-9692
| Abstract »
| Full Text »
| PDF »
- A Mutant Bradyrhizobium japonicum [IMAGE]-Aminolevulinic Acid Dehydratase with an Altered Metal Requirement Functions in Situ for Tetrapyrrole Synthesis in Soybean Root Nodules.
- S. Chauhan and M. R. O'Brian (1995)
J. Biol. Chem.
270, 19823-19827
| Abstract »
| Full Text »
| PDF »
- gsa1 Is a Universal Tetrapyrrole Synthesis Gene in Soybean and Is Regulated by a GAGA Element.
- J. M. Frustaci, I. Sangwan, and M. R. O'Brian (1995)
J. Biol. Chem.
270, 7387-7393
| Abstract »
| Full Text »
| PDF »
- Wild Type Rhizobium etli, a Bean Symbiont, Produces Acetyl-fucosylated, N-Methylated, and Carbamoylated Nodulation Factors.
- Rém. Poupot, E.ér. Martinez-Romero, N. Gautier, and J.-C. Promé (1995)
J. Biol. Chem.
270, 6050-6055
| Abstract »
| Full Text »
| PDF »
- Bacterial symbionts induce host organ morphogenesis during early postembryonic development of the squid Euprymna scolopes.
- M. Montgomery and M McFall-Ngai (1994)
Development
120, 1719-1729
| Abstract »
| PDF »
- Nod factors and nodulation in plants.
- I Vijn, L das Nevas, A van Kammen, H Franssen, and T Bisseling (1993)
Science
260, 1764-1765
| PDF »
- CPP1, a DNA-binding protein involved in the expression of a soybean leghemoglobin c3 gene.
- C. Cvitanich, N. Pallisgaard, K. A. Nielsen, A. C. Hansen, K. Larsen, K. Pihakaski-Maunsbach, K. A. Marcker, and E. O. Jensen (2000)
PNAS
97, 8163-8168
| Abstract »
| Full Text »
| PDF »
|
|