The DOI matches its Crossref record; 41 of the 41 references it cites were found in a registry or an index.
Nitrogen economics of root foraging: Transitive closure of the nitrate–cytokinin relay and distinct systemic signaling for N supply vs. demand
Open accessAbstract
As sessile organisms, root plasticity enables plants to forage for and acquire nutrients in a fluctuating underground environment. Here, we use genetic and genomic approaches in a “split-root” framework—in which physically isolated root systems of the same plant are challenged with different nitrogen (N) environments—to investigate how systemic signaling affects genome-wide reprogramming and root development. The integration of transcriptome and root phenotypes enables us to identify distinct mechanisms underlying “N economy” (i.e., N supply and demand) of plants as a system. Under nitrate-limited conditions, plant roots adopt an “active-foraging strategy”, characterized by lateral root outgrowth and a shared pattern of transcriptome reprogramming, in response to either local or distal nitrate deprivation. By contrast, in nitrate-replete conditions, plant roots adopt a “dormant strategy”, characterized by a repression of lateral root outgrowth and a shared pattern of transcriptome reprogramming, in response to either local or distal nitrate supply. Sentinel genes responding to systemic N signaling identified by genome-wide comparisons of heterogeneous vs. homogeneous split-root N treatments were used to probe systemic N responses in Arabidopsis mutants impaired in nitrate reduction and hormone synthesis and also in decapitated plants. This combined analysis identified genetically distinct systemic signaling underlying plant N economy: ( i ) N supply, corresponding to a long-distance systemic signaling triggered by nitrate sensing; and ( ii ) N demand, experimental support for the transitive closure of a previously inferred nitrate–cytokinin shoot–root relay system that reports the nitrate demand of the whole plant, promoting a compensatory root growth in nitrate-rich patches of heterogeneous soil.
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CHL1 Functions as a Nitrate Sensor in Plants
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Self-citationScheible, W.-R., Morcuende, R., Czechowski, T., Fritz, C., Osuna, D., Palacios-Rojas, N., Schindelasch, D., Thimm, O., Udvardi, M. K., & Stitt, M. (2004) · Plant Physiology · doi:10.1104/pp.104.047019 · Cited by 1,042
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Nitrate in 2020: Thirty Years from Transport to Signaling Networks
Vidal, E. A., Alvarez, J. M., Araus, V., Riveras, E., Brooks, M. D., Krouk, G., Ruffel, S., Lejay, L., Crawford, N. M., Coruzzi, G. M., et al. (2020) · The Plant Cell · doi:10.1105/tpc.19.00748 · Cited by 382
Self-citationDefence on demand: mechanisms behind optimal defence patterns
Meldau, S., Erb, M., & Baldwin, I. T. (2012) · Annals of Botany · doi:10.1093/aob/mcs212 · Cited by 197
de Jong, M., George, G., Ongaro, V., Williamson, L., Willetts, B., Ljung, K., McCulloch, H., & Leyser, O. (2014) · Plant Physiology · doi:10.1104/pp.114.242388 · Cited by 138
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Metadata
- Authors
- Ruffel, S., Krouk, G., Ristova, D., Shasha, D., Birnbaum, K. D., & Coruzzi, G. M.
- Venue
- Proceedings of the National Academy of Sciences
- Published
- 2011-10-24
- Volume
- 108
- Issue
- 45
- Pages
- 18524-18529
- ISSN
- 0027-8424 (ISSN-L)
- 1091-6490
- OpenAlex
- W2104388974
- Cited by
- 401
- References
- 41
- FWCI
- 25.43
- Type
- journal article
- Language
- en
- Open access
- green
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- Ruffel, S., Krouk, G., Ristova, D., Shasha, D., Birnbaum, K. D., & Coruzzi, G. M. (2011). Nitrogen economics of root foraging: Transitive closure of the nitrate–cytokinin relay and distinct systemic signaling for N supply vs. demand. Proceedings of the National Academy of Sciences. https://doi.org/10.1073/pnas.1108684108
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