The DOI matches its Crossref record; 2 of the 2 references it cites were found in a registry or an index.
The Transcriptional Innate Immune Response to flg22. Interplay and Overlap with Avr Gene-Dependent Defense Responses and Bacterial Pathogenesis
Open accessAbstract
Animals and plants carry recognition systems to sense bacterial flagellin. Flagellin perception in Arabidopsis involves FLS2, a Leu-rich-repeat receptor kinase. We surveyed the early transcriptional response of Arabidopsis cell cultures and seedlings within 60 min of treatment with flg22, a peptide corresponding to the most conserved domain of flagellin. Using Affymetrix microarrays, approximately 3.0% of 8,200 genes displayed transcript level changes in flg22 elicited suspension cultures and seedlings. FLARE (Flagellin Rapidly Elicited) genes mostly encode signaling components, such as transcription factors, protein kinases/phosphatases, and proteins that regulate protein turnover. Approximately 80% of flg22-induced genes were also up-regulated in Arabidopsis seedlings treated with cycloheximide. This suggests that many FLARE genes are negatively regulated by rapidly turned-over repressor proteins. Twenty-one tobacco Avr9/Cf-9 rapidly elicited (ACRE) cDNA full-length sequences were used to search for their Arabidopsis orthologs (AtACRE). We identified either single or multiple putative orthologs for 17 ACRE genes. For 13 of these ACRE genes, at least one Arabidopsis ortholog was induced in flg22-elicited Arabidopsis suspension cells and seedlings. This result revealed a substantial overlap between the Arabidopsis flg22 response and the tobacco Avr9 race-specific defense response. We also compared FLARE gene sets and genes induced in basal or gene-for-gene interactions upon different Pseudomonas syringae treatments, and infer that Pseudomonas syringae pv tomato represses the flagellin-initiated defense response.
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Gapped BLAST and PSI-BLAST: a new generation of protein database search programs
Altschul, S. (1997) · Nucleic Acids Research · doi:10.1093/nar/25.17.3389 · Cited by 73,302
Nedd8 Modification of Cul-1 Activates SCFβTrCP-Dependent Ubiquitination of IκBα
Read, M. A., Brownell, J. E., Gladysheva, T. B., Hottelet, M., Parent, L. A., Coggins, M. B., Pierce, J. W., Podust, V. N., Luo, R.-S., Chau, V., et al. (2000) · Molecular and Cellular Biology · doi:10.1128/mcb.20.7.2326-2333.2000 · Cited by 363
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Boller, T., & Felix, G. (2009) · Annual Review of Plant Biology · doi:10.1146/annurev.arplant.57.032905.105346 · Cited by 3,387
Self-citationElicitors, Effectors, and R Genes: The New Paradigm and a Lifetime Supply of Questions
Bent, A. F., & Mackey, D. (2007) · Annual Review of Phytopathology · doi:10.1146/annurev.phyto.45.062806.094427 · Cited by 773
Two Pseudomonas syringae Type III Effectors Inhibit RIN4-Regulated Basal Defense in Arabidopsis
Kim, M. G., da Cunha, L., McFall, A. J., Belkhadir, Y., DebRoy, S., Dangl, J. L., & Mackey, D. (2005) · Cell · doi:10.1016/j.cell.2005.03.025 · Cited by 494
Mishina, T. E., & Zeier, J. (2007) · The Plant Journal · doi:10.1111/j.1365-313x.2007.03067.x · Cited by 444
De Vleesschauwer, D., Chernin, L., & Höfte, M. M. (2009) · BMC Plant Biology · doi:10.1186/1471-2229-9-9 · Cited by 77
Metadata
- Authors
- Navarro, L., Zipfel, C., Rowland, O., Keller, I., Robatzek, S., Boller, T., & Jones, J. D. G.
- Venue
- Plant Physiology
- Publisher
- Oxford University Press (OUP)
- Published
- 2004-06-01
- Volume
- 135
- Issue
- 2
- Pages
- 1113-1128
- ISSN
- 0032-0889 (ISSN-L)
- 1532-2548
- OpenAlex
- W2153422220
- Cited by
- 591
- References
- 2
- FWCI
- 34.49
- Type
- journal article
- Language
- en
- Open access
- bronze
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- Navarro, L., Zipfel, C., Rowland, O., Keller, I., Robatzek, S., Boller, T., & Jones, J. D. G. (2004). The Transcriptional Innate Immune Response to flg22. Interplay and Overlap with Avr Gene-Dependent Defense Responses and Bacterial Pathogenesis. Plant Physiology. https://doi.org/10.1104/pp.103.036749
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