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Organ-specific phosphorus-allocation patterns and transcript profiles linked to P efficiency in wheat Tariq Aziz1,2 & Ricarda Jost2 1University of Agriculture, Faisalabad, Pakistan 2School of Plant Biology, The University of Western Australia ‘smarter’ plants with improved P-use efficiency from: Cordell et al. (2009) Preferred future phosphorus scenarios: A framework for meeting long-term phosphorus needs for global food demand. IWA Publishing. Crop P use efficiency [%] ‘smarter’ plants with improved P-use efficiency 250 200 150 100 50 0 0 10 20 30 40 50 Total P supply to each crop exported [%] from: MacDonald et al. (2012) Environ. Res. Lett. 7 from: http://phosphorusfutures.net. Phosphorus efficient wheat A/Prof Tariq Aziz Osborne and Rengel 2002 Aust. J. Agric. Res. 52 & 53: • screen of 99 wheat genotypes on iron phosphate / phytate as sole P source (deficient vs. sufficient supply) • 4 criteria – shoot DW (-Pi), DW (-Pi) vs. DW (+Pi), [P]int. vs. Pi supplied, shoot DW per unit P in plant • Machete = inefficient genotype (3 criteria) • Chinese 80-55 = efficient genotype (2-3criteria, 3/99 genotypes) 7-day growth on 0.2 mM KH2PO4 7-day growth without phosphate Chinese 80-55 15 cm 15 cm Machete Machete Chinese 80-55 Harvesting scheme 25 day-old P-sufficient seedlings, transferred to nutrient solution with either no Pi or with 200 µM Pi and harvest after 3, 7 and 18 days of treatment Organs harvested: mature vs. fine roots young vs. mature leaves leaf sections = tip / middle / basal Chinese 80-55 maintains higher root biomass = Machete = Chinese 80-55 RGR = rel. growth rate 0 3 7 18 3 7 time after transfer [d] 18 0 3 7 18 3 7 18 * p ≤ 0.05 rel. to Machete time after transfer [d] Aziz et al. (2014) PCE 37 Chinese 80-55 has a ‘smart’ P allocation pattern 18 days after transfer +P (C/M) -P (C/M) young leaf Pi Po +5 +2.5 0 Pi Po -2.5 tip -5 middle +P (C/M) base Pi Po -P (C/M) Pi Po mature leaf tip Pi Po Pi Po middle stem base Pi Po fine roots Pi Po Pi Po Pi Po mature root Aziz et al. (2014) PCE 37 TaPHT1;2 is differentially expressed in sink tissues A = TaPHT1;2 18 days after transfer +P (C/M) -P (C/M) young leaf A B A B = TaIPS1 +5 +2.5 0 B -2.5 tip -5 middle +P (C/M) base A B -P (C/M) -Ct (log2) A B mature leaf tip A B A B middle stem base A B fine roots A B A B A B mature root Aziz et al. (2014) PCE 37 rel. expression level [40 – Ct] TaPHT1;2 is not suppressed by high Pi supply in P-efficient Chinese 80-55 48 46 Young Leaf Base - 18 days after transfer 44 42 = P-sufficient Machete 40 38 ** 36 34 * * 32 26 24 = P-sufficient Chinese 80-55 = P-limited Chinese 80-55 30 28 = P-limited Machete * PT1;2 PT1;5 PT1;8 PT2;1 PT3;1 IPS1 * p ≤ 0.05 rel. to treated Machete Summary of responses in P-limited Chinese 80-55 S young leaf = rel. starch levels R = rel. ribosome # mature leaf +5 +2.5 tip 0 -2.5 -5 middle tip base S R middle base stem fine roots S R = rel. Pi uptake capacity mature root Aziz et al. (2014) PCE 37 Summary of responses in P-sufficient Chinese 80-55 S = rel. starch levels R = rel. ribosome # young leaf mature leaf +5 +2.5 tip 0 -2.5 middle base stem S -5 tip S middle S fine roots = rel. Pi uptake capacity R S base mature root Aziz et al. (2014) PCE 37 Conclusions A phosphorus-efficient wheat cultivar Remobilises P to supply source leaves when P-limited Can quickly convert available Pi into organic compounds for growth Restricts ribosome numbers in P-limited sink tissues to off-set development (?) Why bring post‐genomics into the P‐impoverished bush? Yves Gibon (2014) Commentary in Plant, Cell & Environment 37(6) Sulpice et al. (2014) Plant, Cell & Environment 37(6) Please visit posters in session 3 – P utilisation and signalling in plants ! Acknowledgements School of Plant Biology, UWA: Oliver Berkowitz* Patrick M. Finnegan Collaborators: Zed Rengel, School of Earth & Environment, UWA Hans Lambers * ARC Centre of Excellence for Plant Energy Biology, UWA Australian Research Council Postdoctoral Fellowship Program (PDFP) of the Higher Education Commission of Pakistan (T. Aziz) Thank you!