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Characterization of Ion Contents and Metabolic Responses to Salt Stress of Different Arabidopsis AtHKT1;1 Genotypes and Their Parental Strains

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Molecular Plant 2013年第2期6卷 350-368页

作者： Camilla B. Hill Deepa Jha Antony Bacic mark tester Ute Roessner Australian Centre for Plant Functional Genomics School of Botany University of Melbourne Victoria 3010 Australia Australian Centre for Plant Functional Genomics University of Adelaide Waite Campus Glen Osmond 5064 SA Australia Metabolomics Australia School of Botany University of Melbourne Victoria 3010 Australia Bio21 Molecular Science and Biotechnology Institute University of Melbourne Victoria 3010 Australia ARC Centre of Excellence in Plant Cell Walls School of Botany University of Melbourne Victoria 3010 Australia

Plants employ several strategies to maintain cellular ion homeostasis under salinity stress, including mediat-ing ion fluxes by transmembrane transport proteins and adjusting osmotic pressure by accumulating osmolytes. The HKT （high-affinity potassium transporter） gene family comprises Na^＋ and Na^＋/K^＋ transporters in diverse plant species, with HKT1,1 as the only member in Arabidopsis thaliana. Cell-type-specific overexpression of AtHKT1;1 has been shown to prevent shoot Na^＋ overaccumulation under salinity stress. Here, we analyzed a broad range of metabolites and elements in shoots and roots of different AtHKT1;1 genotypes and their parental strains before and after salinity stress, revealing a reciprocal relationship of metabolite differences between an AtHKT1;1 knockout line （hktl;1） and the AtHKT1;1 overex- pressing lines （E2586 UASGAL4：HKT1;1 and J2731＊UASGAL4：HKT1;1）. Although levels of root sugars were increased after salt stress in both AtHKTI,1 overexpressing lines, E2586 UASGAL4：HKT1;1 showed higher accumulation of the osmopro-tectants trehalose, gentiobiose, and melibiose, whereas J2731＊UASGAL4：HKT1;1 showed higher levels of sucrose and raffinose, compared with their parental lines, respectively. In contrast, the knockout line hktl,1 showed strong increases in the levels of the tricarboxylic acid （TCA） cycle intermediates in the shoots after salt treatment. This coincided with a significant depletion of sugars, suggesting that there is an increased rate of carbon influx into the TCA cycle at a constant rate of C-efflux from the cycle, which might be needed to support plant survival during salt stress. Using correlation analysis, we identified associations between the Na^＋ content and several sugars, suggesting that regulation of sugar metabolism is important in plant responses to salinity stress.

关键词： abiotic stress salinity salt tolerance HKT sodium transporter, metabolomics enhancer trap system.

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.

Transition from a maternal to external nitrogen source in maize seedlings

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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

AtHKT1;1 Mediates Nernstian Sodium Currents in Arabidopsis Root Stelar Cells

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AtHKT1;1 Mediates Nernstian Sodium Currents in Arabidopsis R...

Mobilizing Crop Biodiversity

泛环渤海地区九省市生物化学与分子生物学会——2011年学术交流会

作者： Shaowu Xue Xuan Yao Wei Luo Deepa Jha mark tester Tomoaki Horie Julian I.Schroeder Institute of Molecular Science Shanxi University Division of Biological Sciences Cell and Developmental Biology SectionUniversity of CaliforniaSan DiegoLa JollaCA 92093-0116USA Australian Centre for Plant Functional Genomics University of AdelaideSA 5064Australia

The Arabidopsis AtHKTI;1 protein was identified as a sodium(Na+) transporter by heterologous expression in Xenopus laevis oocytes and Saccharomyces ***,direct comparative in vivo electrophysiological analyses of a plant HKT transporter in wild-type and hkt loss-of-function mutants has not yet been reported and it has been recently argued that heterologous expression systems may alter

关键词： Arabidopsis HKT salinity,Na+ current ion channel.

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Molecular Plant 2020年第10期13卷 1341-1344页

作者： Susan McCouch Zahra Katy Navabi Michael Abberton Noelle L.Anglin Rosa Lia Barbieri Michael Baum Kirstin Bett Helen Booker Gerald L.Brown Glenn J.Bryan Luigi Cattivelli David Charest Kellye Eversole Marcelo Freitas Kioumars Ghamkhar Dario Grattipaglia Robert Henry Maria Cleria Valadares Inglis Tofazzal Islam Zakaria Kehel Paul J.Kersey Graham J.King Stephen Kresovich Emily Marden Sean Mayes Marie Noelle Ndjiondjiop Henry T.Nguyen Samuel Rezende Paiva Roberto Papa Peter W.B.Phillips Awais Rasheed Christopher Richards Mathieu Flouard Maria Jose Amstalden Sampaio Uwe Scholz Paul D.Shaw Brad Sherman S.Evan Staton Nils Stein Jan Svensson mark tester Jose Francisco Montenegro Valls Rajeev Varshney Stephen Visscher Eric von Wettberg Robbie Waugh Peter Wenzl Loren H.Rieseberg Plant Breeding and Genetics School of Integrated Plant SciencesCornell UniversityIthacaNY14853USA DivSeek Global Institute for Food Security110 Gymnasium PlaceUniversity of SaskatchewanSaskatoonSKS7N 0W9Canada lnternational Institute of Tropical Agriculture(IITA) PMB 5320Oyo RdIbadanNigeria International Potato Center(CIP)1895 Avenida La Molina Lima Peru 12Lima 15023Peru Embrapa Genetic Resources and Biotechnology Parque Estacjao BiologicaFinal Av W5 NorteCaixa Postal 0237270770-917-Brasilia DFBrazil International Center for Agricultural Research in the Dry Areas(I CAR DA) Station Exp.INRA-Quich.Rue Hafiane Cherkaoui.Agdal.Rabat-Instituts10111RabatMorocco Department of Plant Sciences University of Saskatchewan51 Campus Dr.SaskatoonSK S7N 5A8Canada Department of Plant Agriculture University of GuelphRm 316Crop Science Bldg50 Stone Rd EGuelphON N1G 2W1Canada Genome Prairie 111 Research DriveSuite 101SaskatoonSKS7N 3R2Canada The James Hutt on Institute Errol RoadInvergowrieDundeeDD25DAUK CREA Research Centre for Genomics and Bioinformaticsvia San Protaso 302Fiorenzuola d'Arda29017Italy Genome British Columbia 400-575 West 8th AvenueVancouverBCV5Z 0C4Canada International Wheat Genome Sequencing Consortium 2841 NE Marywood CtLee's SummitMO.64086USA Forage Science Grasslands Research CentreAgResearchPalmerston North4410New Zealand Queensla nd Alliance for Agriculture and Food Inn ovation University of QueenslandBrisbaneQLD 4072Australia Institute of Biotechnology and Genetic Engineering(IBGE) Bangabandhu Sheikh Mujibur Rahman Agricultural UniversityGazipur 1706Bangladesh Southern Cross University PO Box 157LismoreNSW 2480Australia Royal Botanic Gardens KewRichmondSurreyTW93AEUK Feed the Future Innovation Lab for Crop Improvement 431 Weill HallCornell UniversityIthacaNY14853USA Department of Botany and Biodiversity Research Centre University of British ColumbiaVancouverBC V6R 2A5Canada Crops For the Future(UK)CIC 76-80 Baddow Road ChelmsfordEs

Over the past 70 years,the world has witnessed extraordinary growth in crop productivity,enabled by a suite of technological advances,including higher yielding crop varieties,improved farm management,synthetic agrochemicals,and agricultural *** this"Green Revolution"intensified crop production,and is credited with reducing famine and malnutrition,its benefits were accompanied by several undesirable collateral effects(Pingali,2012).These include a narrowing of agricultural biodiversity,stemming from increased monoculture and greater reliance on a smaller number of crops and crop varieties for the majority of our *** reduction in diversity has created vulnerabilities to pest and disease epidemics,climate variation,and ultimately to human health(Harlan,1972).

关键词： intensified crops agricultural