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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, Pakistan2School of Plant Biology, The University of Western Australia
from: Cordell et al. (2009) Preferred future phosphorus scenarios: A framework for meeting long-term phosphorus needs for global food demand. IWA Publishing.
‘smarter’ plants with improved P-use efficiency
from: http://phosphorusfutures.net.
‘smarter’ plants with improved P-use efficiency
from: MacDonald et al. (2012) Environ. Res. Lett. 7
Cro
p P
use
eff
icie
ncy
[%
]250
200
150
100
50
0100 20 30 40 50
Total P supply to each crop exported [%]
15 cm
15 cm
Machete Chinese 80-55
7-day growth on 0.2 mM KH2PO4
Machete Chinese 80-55
7-day growth without phosphate
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)
Harvesting scheme
25 day-old P-sufficient seedlings, transferred to nutrient solution with either no Pi orwith 200 µM Pi and harvest after 3, 7 and 18 days of treatment
Organs harvested: mature vs. fine rootsyoung vs. mature leavesleaf sections = tip / middle / basal
Aziz et al. (2014) PCE 37
= Machete
= Chinese 80-55
Chinese 80-55 maintains higher root biomass
* p ≤ 0.05 rel. to Machete
RGR = rel. growth rate
time after transfer [d] time after transfer [d]
0 3 7 18 3 7 18 0 3 7 18 3 7 18
Chinese 80-55 has a ‘smart’ P allocation pattern
+P (C/M) -P (C/M)
Pi Po Pi Po
Pi Po Pi Po
Pi Po Pi Po
Pi Po Pi Pofine roots
stem
mature root
mature leaf
young leaf
tip
middle
base
base
middle
tip
Pi Po Pi Po
Aziz et al. (2014) PCE 37
+5
+2.5
0
-2.5
-5
+P (C/M) -P (C/M)
18 days after transfer
TaPHT1;2 is differentially expressed in sink tissues
+P (C/M) -P (C/M)
A B A B
A B A B
A B A B
A B A Bfine roots
stem
mature root
mature leaf
young leaf
tip
middle
base
base
middle
tip
A B A B
Aziz et al. (2014) PCE 37
+5
+2.5
0
-2.5
-5
-Ct (log2)
A = TaPHT1;2 B = TaIPS1
+P (C/M) -P (C/M)
18 days after transfer
= P-sufficient Machete
= P-limited Chinese 80-55
= P-limited Machete
= P-sufficient Chinese 80-55
TaPHT1;2 is not suppressed by high Pi supplyin P-efficient Chinese 80-55
* p ≤ 0.05 rel. to treated Machete
rel.
expr
essi
on le
vel [
40 –
C
t]
PT2;1 PT3;1 IPS1PT1;5 PT1;8PT1;2
Young Leaf Base
24
26
28
30
32
34
36
38
40
42
44
46
48
*
- 18 days after transfer
Summary of responses in P-limited Chinese 80-55
fine roots
stem
mature root
tip
middle
base
base
middle
tip
Aziz et al. (2014) PCE 37
+5
+2.5
0
-2.5
-5
S
S R
R
mature leafyoung leaf
= rel. starch levelsS = rel. ribosome #R
= rel. Pi uptake capacity
Summary of responses in P-sufficient Chinese 80-55
fine roots
stem
mature root
tip
middle
base
Aziz et al. (2014) PCE 37
+5
+2.5
0
-2.5
-5
middle
S
mature leafyoung leaf
S
S
= rel. starch levelsS = rel. ribosome #R
= rel. Pi uptake capacity
baseR S
tip
Conclusions
A phosphorus-efficient wheat cultivar
Þ Remobilises P to supply source leaves when P-limited
Þ Can quickly convert available Pi into organic compounds for growth
Þ Restricts ribosome numbers in P-limited sink tissues to off-setdevelopment (?)
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 !
Collaborators:
Zed Rengel, School of Earth & Environment, UWA
Acknowledgements
Australian Research Council
School of Plant Biology, UWA:
Oliver Berkowitz*
Patrick M. Finnegan
Hans Lambers
Postdoctoral Fellowship Program (PDFP) of the Higher Education Commission of Pakistan (T. Aziz)
* ARC Centre of Excellence for Plant Energy Biology, UWA