Nod Signal Recognition

 

 

Chitin/ lipo-chitin recognition by plants

Agonist recognition by a receptor protein leading to the activation of a signal transduction pathway is a key event in many important cellular processes (e.g., organogenesis). The molecular mechanisms of sensory perception in plants are largely unknown. We are studying the nitrogen-fixing symbiosis between the bacterium, Bradyrhizobium japonicum, and soybean. B. japonicum infects soybean roots and induces the formation of a nodule, a new organ, in which the bacteria reside. Nodule organogenesis is induced by substituted lipo-chitin molecules synthesized by the products of the bacterial nodulation genes. Past work from our laboratory has identified the lipo-chitin molecules produced by B. japonicum and explored their biosynthesis. Structure/ function studies suggest that the lipo-chitin Nod signals are recognized by two receptors. One receptor shows limited specificity, since unsubstituted, chitin oligomers are active. The second receptor requires a specific Nod signal.

The lipo-chitin Nod signals resemble simple chitin oligomers, which are known to induce plant defense responses. Indeed, it is our hypothesis that the Nod signal recognition pathway likely evolved from a more ancient chitin sensing system found in all plants. This has led us to examine the chitin response in plants. Using DNA microarray analysis, we have identified a number of genes in the model plants Arabidopsis thaliana and Medicago truncatula that respond to chitin treatment (Ramonell et al., 2002; Zhang et al., 2002). Our data suggest that Arabidopsis possesses two chitin-recognition pathways; one, responds to higher molecular weight chitin oligomers resulting in induction of pathogen defense pathways and two, a pathway that responds to lower molecular weight oligomers.  Zhang et al. (2002) demonstrated that the first pathway is unique and unrelated to the well characterized pathways involving salicylic acid, ethylene or jasmonic acid. Most recently, Wan et al. (2004) demonstrated that this pathway activates a MAP kinase cascade resulting in the activation of WRKY family transcriptional regulators.

Hierarchical cluster of 166 Arabidopsis ESTs with significant changes (>2.5-fold) in transcription level in response to chitin treatment. Each gene is represented by a single row of colored boxes, and each time point is represented by a single column. Induction (or repression) ranges from pale to saturated red (or green). The data represent an average of two independent experiments.
©Copyright, 2002.

 

 

Recent publications relating to this research topic:

           

            Ramonell, K., B. Zhang, R. Ewing, Y. Chen, D. Xu, G. Stacey, and S. Somerville. 2002 Microarray analysis of chitin

            elicitation in Arabidopsis thaliana. Mol. Plant Pathol. 3 (1): 301-311.
 

            Zhang, B., K. Ramonell, S. Somerville, and G. Stacey. 2002. Characterization of Early, Chitin-Induced Gene Expression in

            Arabidopsis Mol. Plant-Microbe Int. 15: 963-970

 

            Wan, Jinrong, Shuqun Zhang, and Gary Stacey. 2004.  Activation of a potential mitogen-activated protein kinase pathway in

             Arabidopsis by chitin. Mol. Plant Pathol. 5(1): 125-135.

 

            Ramonell K, Berrocal-Lobo M, Koh S, Wan J, Edwards H, Stacey G and Somerville S. 2005. Loss-of-function mutations in four chitin responsive genes show

             increased susceptibility to the powdery mildew pathogen, Erysiphe cichoracearum. Plant Physiol. 138: 1027-1036

 

           

 

A portion of the work presented was supported by the Department of Energy, Basic Energy Biosciences Program under Grant No. DE-FG02-97ER20260. Any opinions, findings, and conclusions or recommendations expressed in this material are those of the author(s) and do not necessarily reflect the views of the Department of Energy.

 

 


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