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Transition from a maternal to external nitrogen source in maize seedlings

Journal of Integrative Plant Biology 2017年第4期59卷 261-274页

作者： Kasra Sabermanesh Luke R. Holtham Jessey George Ute Roessner Berin A. Boughton Sigrid Heuer Mark Tester darren C. plett Trevor P. Garnett Australian Centre for Plant Functional Genomics Waite Research Institute University of Adelaide Adelaide SA 5064 Australia School of Agriculture Food and Wine Waite Research Institute University of Adelaide Adelaide SA 5064 Australia Australian Centre for Plant Functional Genomics School of BioSciences University of Melbourne Parkville Vic. 3010 Australia Metabolomics Australia School of BioSciences University of Melbourne Vic. 3010 Australia King Abdullah University of Science and Technology Center for Desert Agriculture Thuwal 23955-6900 Kingdom of Saudi Arabia6. The Australian Plant Phenomics Facility The Plant Accelerator Waite Campus The University of Adelaide Adelaide SA 5064 Australia The Australian Plant Phenomics Facility The Plant Accelerator Waite Campus The University of Adelaide Adelaide SA 5064 Australia

Maximizing NO3 uptake during seedling development is important as it has a major influence on plant growth and yield. However, little is known about the processes leading to, and involved in, the initiation of root NO3 uptake capacity in developing seedlings. This study examines the physiological processes involved in root NO3 uptake and metabolism, to gain an understanding of how the NO3 uptake system responds to meet demand as maize seedlings transition from seed N use to external N capture. The concentrations of seedderived free amino acids within root and shoot tissues are initially high, but decrease rapidly until stabilizing eight days after imbibition （DAI）. Similarly, shoot N% decreases, but does not stabilize until 12-13 DAI. Following the decrease in free amino acid concentrations, root NO3- uptake capacity increases until shoot N% stabilizes. The increase in root NO3 uptake capacity corresponds with a rapid rise in transcript levels of putative NO3 transporters, ZmNRT2.1 and ZmNRT2.2. The processes underlying the increase in root NO3- uptake capacity to meet N demand provide an insight into the processes controlling N uptake.

关键词： NRT Transition from a maternal to external nitrogen source in maize seedlings NO

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Root-Specific Transcript Profiling of Contrasting Rice Genotypes in Response to Salinity Stress

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Molecular Plant 2011年第1期4卷 25-41页

作者： Olivier Cotsaftis darren plett Alexander A.T. Johnson Harkamal Walia Clyde Wilson Abdelbagi M. Ismail Timothy J. Close Mark Tester Ute Baumann Australian Centre for Plant Functional Genomics Private Mail Bag 1 Glen Osmond SA 5064 Australia Present address: School of Botany University of Melbourne Parkville Vic 3010 Australia Department of Botany and Plant Sciences University of California Riverside CA 92521 USA Present address: Department of Agronomy and Horticulture University of Nebraska Lincoln NE 68588 USA United States Department of Agriculture Agricultural Research Service George E. Brown Jr Salinity Laboratory Riverside CA 92507 USA International Rice Research Institute Manila The Philippines

Elevated salinity imposes osmotic and ion toxicity stresses on living cells and requires a multitude of responses in order to enable plant survival. Building on earlier work profiling transcript levels in rice （Oryza sativa） shoots of FL478, a salt-tolerant indica recombinant inbred line, and IR29, a salt-sensitive cultivar, transcript levels were compared in roots of these two accessions as well as in the roots of two additional salt-tolerant indica genotypes, the landrace Pokkali and the recombinant inbred line IR63731. The aim of this study was to compare transcripts in the sensitive and the tolerant lines in order to identify genes likely to be involved in plant salinity tolerance, rather than in responses to salinity perse. Transcript profiles of several gene families with known links to salinity tolerance are described （e.g. HKTs, NHXs）. The putative function of a set of genes identified through their salt responsiveness, transcript levels, and/or chro- mosomal location （i.e. underneath QTLs for salinity tolerance） is also discussed. Finally, the parental origin of the Saltol region in FL478 is further investigated. Overall, the dataset presented appears to be robust and it seems likely that this system could provide a reliable strategy for the discovery of novel genes involved in salinity tolerance.

关键词： Rice root salinity tolerance microarray HKT Saltol.

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