Ethylene is critical to the maintenance of primary root growth and Fe. homeostasis under Fe stress in Arabidopsis

Similar documents
Figure 1. Identification of UGT74E2 as an IBA glycosyltransferase. (A) Relative conversion rates of different plant hormones to their glucosylated

Supplemental Data. Perrella et al. (2013). Plant Cell /tpc

Supplemental Figure 1: Increased Fe deficiency gene expression in roots of nas4x-2

** * * * Col-0 cau1 CAU1. Actin2 CAS. Actin2. Supplemental Figure 1. CAU1 affects calcium accumulation.

GFP GAL bp 3964 bp

SUPPLEMENTARY INFORMATION

SUPPLEMENTARY INFORMATION

Supplementary Figure 1 Characterization of wild type (WT) and abci8 mutant in the paddy field.

Table S1 List of primers used for genotyping and qrt-pcr.

Supplementary Figure 1

Supplemental Data. Wang et al. (2014). Plant Cell /tpc

Nature Genetics: doi: /ng Supplementary Figure 1. The phenotypes of PI , BR121, and Harosoy under short-day conditions.

Supporting Online Material

Supplemental Data. Fernández-Calvo et al. Plant Cell. (2011) /tpc

Heterosis and inbreeding depression of epigenetic Arabidopsis hybrids

POTASSIUM IN PLANT GROWTH AND YIELD. by Ismail Cakmak Sabanci University Istanbul, Turkey

Supplementary Figure S1. Amino acid alignment of selected monocot FT-like and TFL-like sequences. Sequences were aligned using ClustalW and analyzed

Growth and development of Arabidopsis thaliana under single-wavelength red

Supplemental Data. Chen and Thelen (2010). Plant Cell /tpc

GENETIC ANALYSES OF ROOT SYSTEM DEVELOPMENT IN THE TOMATO CROP MODEL

Supplementary Figure 1. Phenotype of the HI strain.

Supplementary Materials for

Supplemental Figure 1. Phenotype of ProRGA:RGAd17 plants under long day

Supplemental Figure 1. Comparison of Tiller Bud Formation between the Wild Type and d27. (A) and (B) Longitudinal sections of shoot apex in wild-type

Supplemental Data. Hou et al. (2016). Plant Cell /tpc

Regulation of Phosphate Homeostasis by microrna in Plants

Supplemental Data. Perea-Resa et al. Plant Cell. (2012) /tpc

Supplementary Material. stress responsive genes providing protection of wheat from salinity stress

Hormonal and other chemical effects on plant growth and functioning. Bill Davies Lancaster Environment Centre, UK

The sucrose non-fermenting-1-related protein kinases SAPK1 and SAPK2 function collaboratively as positive regulators of salt stress tolerance in rice

Characterisation of abiotic stress inducible plant promoters and bacterial genes for osmotolerance using transgenic approach

Radicle emergence (%)

Photoreceptor Regulation of Constans Protein in Photoperiodic Flowering

Nature Biotechnology: doi: /nbt Supplementary Figure 1. Generation of paraxial mesoderm from the H7 hesc line.

SUPPLEMENTARY INFORMATION

23-. Shoot and root development depend on ratio of IAA/CK

Numerical Data. Effect of copper on nutrients content (mg g 1 dry wt.) of radish (45th day) N P K Na Ca Mg

Localized Iron Supply Triggers Lateral Root Elongation in Arabidopsis by Altering the AUX1-Mediated Auxin Distribution C W OA

Maria V. Yamburenko, Yan O. Zubo, Radomíra Vanková, Victor V. Kusnetsov, Olga N. Kulaeva, Thomas Börner

Ethylene Mediates Response and Tolerance to Potassium Deprivation in Arabidopsis W

Supporting Online Material for

Supp- Figure 2 Confocal micrograph of N. benthamiana tissues transiently expressing 35S:YFP-PDCB1. PDCB1 was targeted to plasmodesmata (twin punctate

Supplemental Figures. Supplemental Data. Sugliani et al. Plant Cell (2016) /tpc Clades RSH1. Rsh1[HS] RSH2 RSH3. Rsh4[HS] HYD TGS ACT

Supplemental Table 1. Primers used for cloning and PCR amplification in this study

Supplementary Materials for

Heterozygous BMN lines

Supplemental Data. Yamamoto et al. (2016). Plant Cell /tpc WT + HCO 3. slac1-4/δnc #5 + HCO 3 WT + ABA. slac1-4/δnc #5 + ABA

UNIVERSITY OF CAMBRIDGE INTERNATIONAL EXAMINATIONS International General Certificate of Secondary Education

Nicotianamine Functions in the Phloem-Based Transport of Iron to Sink Organs, in Pollen Development and Pollen Tube Growth in Arabidopsis C W

HRS1 Acts as a Negative Regulator of Abscisic Acid Signaling to Promote Timely Germination of Arabidopsis Seeds

Title: Iron-Nicotianamine Transporters are Required for Proper Long Distance Iron Signaling

Auxin and Light Control of Adventitious Rooting in Arabidopsis Require ARGONAUTE1 W

efp Visualization of Polysomal mrnas ( Translatomes ) in Discrete Cell Populations of Arabidopsis Seedlings: Control and Hypoxia Stressed

Nature Genetics: doi: /ng Supplementary Figure 1. ssp mutant phenotypes in a functional SP background.

Supplementary Figure 1 Analysis of beige fat and cells and characteristics of exosome release, related to Figure 1

DEVELOPMENTAL GENETICS OF ARABIDOPSIS THALIANA

SUPPORTING INFORMATION. A New Approach for the Surface Enhanced Resonance Raman Scattering (SERRS)

Cytokinin. Fig Cytokinin needed for growth of shoot apical meristem. F Cytokinin stimulates chloroplast development in the dark

Cells: 3 Star. Which row in the chart below best explains the movement of some molecules between the model cell and the solution in the beaker?

. Supplementary Information

Lipid transfer proteins confer resistance to trichothecenes

Supplementary Figure 1. Nature Genetics: doi: /ng.3848

AP Biology Plant Control and Coordination

The bhlh Transcription Factor POPEYE Regulates Response to Iron Deficiency in Arabidopsis Roots W OA

RNA-seq to study rice defense responses upon parasitic nematode infections. Tina Kyndt

Supplementary Figure 1. Markedly decreased numbers of marginal zone B cells in DOCK8 mutant mice Supplementary Figure 2.

Genetic interaction and phenotypic analysis of the Arabidopsis MAP kinase pathway mutations mekk1 and mpk4 suggests signaling pathway complexity

Useful Propagation Terms. Propagation The application of specific biological principles and concepts in the multiplication of plants.

Arabidopsis thaliana. Lucia Strader. Assistant Professor, Biology

Waithe et al Supplementary Figures

Development 143: doi: /dev : Supplementary information

Penghui Li, Beibei Chen, Gaoyang Zhang, Longxiang Chen, Qiang Dong, Jiangqi Wen, Kirankumar S. Mysore and Jian Zhao

EXPRESSION OF THE FIS2 PROMOTER IN ARABIDOPSIS THALIANA

PYR1 PYL1 PYL2 PYL3 PYL4 PYL5 PYL6 PYL7 PYL8 PYL9 PYL10 PYL11/12

ESR1 Allele Frequency. PIK3CA Allele Frequency

Highly Efficient Flexible Solar Cells Based on Room-Temperature

m1 m2 m3 m4 m5 m6 m7 m8 wt m m m m m m m m8 - + wt +

Working with Mycorrhizas in Forestry and Agriculture

Biological Roles of Cytokinins

Analysis of regulatory function of circadian clock. on photoreceptor gene expression

Supplemental material

Surface Analytical Techniques for Analysis of Coatings Mary Jane Walzak, Mark Biesinger and Brad Kobe The University of Western Ontario, Surface

ABI4 Mediates Abscisic Acid and Cytokinin Inhibition of Lateral Root Formation by Reducing Polar Auxin Transport in Arabidopsis C W

Supplementary Figure 1. Real time in vivo imaging of SG secretion. (a) SGs from Drosophila third instar larvae that express Sgs3-GFP (green) and

Stomata and water fluxes through plants

Figure S1. Programmed cell death in the AB lineage occurs in temporally distinct

Supplementary Figure 1. Nature Biotechnology: doi: /nbt.4067

Measuring plant response to virus infection and water stress

Transitivity-dependent and transitivity-independent cell-to-cell movement of RNA

SUPPLEMENTARY INFORMATION

Nature Genetics: doi: /ng Supplementary Figure 1. The FIN and FAB genes act separately from the meristem maturation pathway.

GFP WxTP-GFP WxTP-GFP. stromules. DsRed WxTP-DsRed WxTP-DsRed. stromules

Iron- and Ferritin-Dependent Reactive Oxygen Species Distribution: Impact on Arabidopsis Root System Architecture

bhlh transcription factor bhlh115 regulates iron homeostasis

Supplementary Figure 1: Mechanism of Lbx2 action on the Wnt/ -catenin signalling pathway. (a) The Wnt/ -catenin signalling pathway and its

Arabidopsis NPCC6/NaKR1 Is a Phloem Mobile Metal Binding Protein Necessary for Phloem Function and Root Meristem Maintenance C W

Arabidopsis ASA1 Is Important for Jasmonate-Mediated Regulation of Auxin Biosynthesis and Transport during Lateral Root Formation W OA

expression of AUX1, LAX1, LAX2 and LAX3 in etiolated hypocotyls.

Supporting Information

Supplementary Information for: Giant Kiruna-type deposits form by. efficient flotation of magmatic magnetite suspensions

Transcription:

Ethylene is critical to the maintenance of primary root growth and Fe homeostasis under Fe stress in Arabidopsis Guangjie Li, Weifeng Xu, Herbert J. Kronzucker, Weiming Shi * Supplementary Data

Supplementary data Supplementary Fig. S1 The effect of ph on primary root growth in Arabidopsis (Col-0) when roots are supplied with or without excess Fe. Seedlings at five days after germination (five DAG) were transferred to varying ph conditions in the root growth medium (bottom part) with or without Fe [provided as Fe-EDTA] and grown for an additional five days, after which root growth was measured. ph = 5.7 was used as the control. Data represent means of seven or more plants ± SE (error bars are not visible due to overlap with legend marks). Different letters represent means statistically different at the 0.05 level (one-way ANOVA analysis with Duncan post-hoc test). 2

Supplementary Fig. S2 The effect on the lateral root number and chlorophyll content in Arabidopsis when roots are supplied with Fe-EDTA. Seedlings at five days after germination (five DAG) were transferred to serial concentrations of Fe-EDTA and grown for an additional five days. (A) Lateral root number of five-day-old wild-type exposed to serial concentrations of Fe [provided as Fe-EDTA] for five days. Data represent means of eight or more plants ± SE. (B) Chlorophyll content of five-day-old wild-type exposed to serial concentrations Fe for five days. Values are means ± SE of three replicates. Different letters represent means statistically different at the 0.05 level (one-way ANOVA analysis with Duncan post-hoc test). FW, fresh weight. 3

Supplementary Fig. S3 Effect of excess Fe on the activity of the EBS::GUS in Arabidopsis root tissue. Seedlings at four DAG were exposed to 350 M in the roots for four days, and then ethylene reporter EBS::GUS activity was determined. One representative sample from each treatment (10 plants) is shown. Scale of bars = 100 m. a. primary root tips. b. stele of primary root. 4

Supplementary Fig. S4 The effect of AVG on eto1-1 primary root growth under excess Fe stress. Five-day-old wild-type and eto1-1 seedlings were transferred to medium roots supplemented with 350 M Fe alone or in combination with 1 M AVG for five days. Values are the means ± SE, n 5. Primary root growth in wild type in control under mock or AVG conditions was 5.3 ± 0.12 and 5.34 ± 0.35 cm, respectively. In eto1-1, in control under mock or AVG conditions, it was 3.08 ± 0.27 and 3.84 ± 0.11 cm, respectively. Different letters represent means statistically different at the 0.05 level for a given genotype (one-way ANOVA analysis with Duncan post-hoc test). 5

Supplementary Fig. S5 Effect of excess Fe on the staining of CycB1::GUS and QC25::GUS in medium supplemented with or without AVG. Five-day-old wild-type seedlings were transferred to medium roots supplemented with 350 M Fe alone or in combination with 1 M AVG for three days. (A) to (C) CycB1::GUS staining; (D) QC25::GUS staining. Values are the means ± SE, n = 5. Different letters represent means statistically different at the 0.05 level (one-way ANOVA analysis with Duncan post-hoc test). 6

Supplementary Fig. S6 Analysis of iron plaque formation on the root surface of Arabidopsis WT and eto1-1 mutant. Five-day-old wild-type and eto1-1 seedlings were transferred to control or excess Fe medium with or without AVG for an additional five days of growth, and then the materials formed on the Arabidopsis roots were observed and analyzed using an optical microscope or SEM/EDX. (A) Energy-dispersive X-ray spectra (EDX) of the Arabidopsis root surface as described by Mi et al. (2013). More than seven independent seedlings were analyzed. wt%, weight percentage (%) of the Fe in the root surface. (B) Optical microscope images of Arabidopsis roots. One representative sample for each experiment is shown. Scale bars = 100 m. 7

Supplementary Fig. S7 Fe 3+ staining in roots of Arabidopsis WT and eto1-1 seedlings. Five-day-old wild-type and eto1-1 seedlings were transferred to medium roots supplemented with 350 M Fe alone or in combination with 1 M AVG for four days. Localization of ferric Fe was analyzed by Perl s staining as described by Stacey et al. (2008). Scale bars = 50 m. 8

Supplementary Fig. S8 Effect of ethylene on tissue mineral contents in excess Fe-treated seedlings. The effect of ethylene on mineral contents in shoots and roots of Arabidopsis WT and eto1-1 seedlings in roots supplemented with 350 M Fe alone or in combination with 1 M AVG for five days. Values are the means ± SE of three replicates. Different letters represent means statistically different at the 0.05 level (one-way ANOVA analysis with Duncan post-hoc test). DW, dry weight. 9

Supplementary Fig. S9 The effect of exogenous K + on primary root growth in wild-type and eto1-1 seedlings. Five-day-old wild-type and eto1-1 seedlings were transferred to medium supplemented with 350 M Fe plus varying K + [provided as K 2 SO 4 ] concentrations in the root medium. Values are the means ± SE, n 7. Primary root growth in wild-type and eto1-1 in control was 5.3 ± 0.2 and 3.03 ± 0.24 cm, respectively. Different letters represent means statistically different at the 0.05 level for a given genotype (one-way ANOVA analysis with Duncan post-hoc test). 10

Supplementary Fig. S10 The effect of excess Fe treatment on AtHAK5 and AtAKT1 transcript levels in eto2-1 mutants. Expression of HAK5 and AKT1 were determined by quantitative RT-PCR after exposure of five-day-old WT and eto2-1 seedlings to 350 M Fe for 6 hours. The relative mrna level was normalized to the CBP20 expression. Values are means ± SE of three replicates. 11

Supplementary Fig. S11. Effect of excess Fe on the expression of AtFRD3 gene and the specific analysis of primers used for RT-PCR. (A) The specific analysis of primers used for RT-PCR. Primer specificity was confirmed by ordinary PCR, as follows: 94 C for 5 min followed by 35 cycles of 94 C for 20 s, 60 C for 20 s, and 72 C for 30 s. (B) Expression of FRD3 was determined by quantitative RT-PCR after exposure of five-day-old WT and eto1-1 seedlings to 350 M Fe for 6 hours. The relative mrna level was normalized to the CBP20 expression. Values are means ± SE of three replicates. 12

Table S1 Gene-specific primers used for RT-PCR. Gene Forward Primers (5'-3') Reverse Primers (5'-3') HAK5 CGAGACGGACAAAGAAGAGGAACC CACGACCCTTCCCGACCTAATCT AKT1 GAGGAGTATCCAATGACCTGCTTT TGTTCCAGTATCTACATCCACCAA FRD3 TTTGTCGGGCGTTTAGG TGCTGTGGCTGGTTGGT FER1 TCCCATTGGATGTAGCACGAG GATTAGCGGCGGTGAAAGAC FER2 CAGCTAAGAAGAATAGGAAAGGGTC TTAAGTACACACTCACAAGCATTCG FER3 CTTGCTCGTCATTTGTACTCCC TGTAACTTGACCCTCCCACCAC FER4 TTAACGAGCAGATCAATGTGGAAT CACCACGTTTGTTCTGATACTCCA ACS2 TCATGGGAAAAGCTAGAGGTGGAAG TCAACGGTTAATTTGAAATTGTCGG ACS7 CCTGGGTTCCGTGAAAACGCATT CGTCGTTAGGATCGGCGAGAATGA ACS8 TGGGGTGATTTACTCCAACGATGATT GACACTCGATGCCTGCAGCCTCTAG ACS11 CTGGTTTCGGGTCTAAAGGAAGCGG AATGACACGATGAGCCTGGAGAGATGTT ACO1 CCGTGTAATGACAGTGAAGCATGGAAG TCTCAAGTCTGGGGCCTTTGTCTCC ACO2 GGATGTCGGTTGCATCGTTTTA TACGGCTGCTGTAGGATTCAGTTC CBP20 ACCATCGGAAACGACAAAGAG CTTCACCATCGTCATCGGAGT 13