Species & Dataset
Experiment
Foliar Ozone Injury
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Oryza sativa
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Common name: Asian rice
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Family: Poaceae
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Cultivar: cv. Nipponbare; O. sativa L. japonica-type
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Tissue: Third and fourth leaves of 2-week old rice plant
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Ozone concentration: 0.2 ppm
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Ozone exposure: 24 hours
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Sampling time: 0, 6, 12 and 24 hrs after ozone treatment
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Platform: DNA Microarray
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Year of study: 2008
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Location: Japan

Title: Integrated Transcriptomics, Proteomics, and Metabolomics analyses to survey ozone responses in the leaves of rice seedling
Summary: Ozone (O3), a serious air pollutant, is known to significantly reduce photosynthesis, growth, and yield and to cause foliar injury and senescence. Here, integrated transcriptomics, proteomics, and metabolomics approaches were applied to investigate the molecular responses of O3 in the leaves of 2-week-old rice (cv. Nipponbare) seedlings exposed to 0.2 ppm O3 for a period of 24 h. On the basis of the morphological alteration of O3-exposed rice leaves, transcript profiling of rice genes was performed in leaves exposed for 1, 12, and 24 h using rice DNA microarray chip. A total of 1535 non redundant genes showed altered expression of more than 5-fold over the control, representing 8 main functional categories. Genes involved in information storage and processing (10%) and cellular processing and signaling categories (24%) were highly represented within1h of O3 treatment; transcriptional factor and signal transduction, respectively, were the main subcategories. Genes categorized into information storage and processing (17, 23%), cellular processing and signaling (20, 16%) and metabolism (18, 19%) were mainly regulated at 12 and 24 h; their main subcategories were ribosomal protein, posttranslational modification, and signal transduction and secondary metabolites biosynthesis, respectively. Two dimensional gel electrophoresis-based proteomics analyses in combination with tandem mass spectrometer identified 23 differentially expressed protein spots (21 non redundant proteins) in leaves exposed to O3 for 24 h compared to respective control.Identified proteins were found to be involved in cellular processing and signaling (32%), photosynthesis (19%), and defense (14%). Capillary electrophoresis-mass spectrometry-based metabolomic profiling revealed accumulation of amino acids, gamma-aminobutyric acid, and glutathione in O3 exposed leaves until 24 h over control. This systematic survey showed that O3 triggers a chain reaction of altered gene, protein and metabolite expressions involved in multiple cellular processes in rice.
Reference: Cho, K., Shibato, J., Agrawal, G.K., Jung, Y.H., Kubo, A., Jwa, N.S., Tamogami, S., Satoh, K., Kikuchi, S., Higashi, T. and Kimura, S., 2008. Integrated transcriptomics, proteomics, and metabolomics analyses to survey ozone responses in the leaves of rice seedling. Journal of proteome research, 7(7), pp.2980-2998.
Gene Identifier | Gene Code | Uniprot ID | Bin Code | Bin Name | FoldChange (1hr) | FoldChange (12hr) | FoldChange (24hr) | Functional annotation |
|---|---|---|---|---|---|---|---|---|
AK071136 | LOC_Os03g55030 | 26.2 | misc.UDP glucosyl and glucoronyl transferases | NA | 0.10 | NA | P. vulgaris UDP-glucosyltransferase HRA25 mRNA, complete cds.|PLN | |
AK071453 | #N/A | #N/A | #N/A |
NA |
6.13 |
NA |
O. sativa class III chitinase RCB4 (Rcb4) mRNA, complete cds.|PLN | |
AK071664 | LOC_Os02g17534 | 10.3 | cell wall.hemicellulose synthesis | 8.86 | 6.29 | NA | P. sativum xyloglucan fucosyltransferase mRNA, complete cds.|PLN | |
AK071812 | LOC_Os03g20120 | 3.1.1.2 | minor CHO metabolism.raffinose family.galactinol synthases.putative | 6.76 | NA | NA | O. sativa mRNA for WSI76 protein induced by water stress: (Glycosyltransferase) | |
AK071889 | LOC_Os07g35560 | 26.4 | misc.beta 1,3 glucan hydrolases | NA | 8.78 | 12.76 | A. thaliana clone 7119 mRNA, complete sequence.|PLN | |
AK072074 | LOC_Os06g09450 | P30298 | 2.2.1.5 | major CHO metabolism.degradation.sucrose.Susy | NA | 21.81 | 14.31 | O. sativa mRNA for sucrose synthase.|PLN |
AK072339 | #N/A | #N/A | #N/A | NA | 0.10 | 0.18 | O. sativa soluble starch synthase II-1 mRNA, complete cds.|PLN | |
AK098880 | LOC_Os03g55070 | Q9AUV6 | 10.1.4 | cell wall.precursor synthesis.UGD | 7.96 | NA | NA | G. max UDP-glucose dehydrogenase mRNA, complete cds.|PLN |
AK099698 | LOC_Os02g50490 | Q6Z5P2 | 10.6.1 | cell wall.degradation.cellulases and beta -1,4-glucanases | NA | 6.58 | 5.06 | A. thaliana putative glucanse (At2g32990; T21L14.7) mRNA, complete cds.|PLN |
AK100416 | LOC_Os05g46260 | Q53WK1 | 26.2 | misc.UDP glucosyl and glucoronyl transferases | 10.50 | 11.12 | NA | D. melanogaster clone GH02288 BcDNA.GH02288 mRNA: (putative glycosyltransferase) |
AK100908 | LOC_Os03g16980 | 10.1.5 | cell wall.precursor synthesis.UXS | NA | 8.50 | 5.60 | O. sativa UXS-2 mRNA for UDP-glucuronic acid decarboxylase, complete cds.|PLN | |
AK100910 | LOC_Os05g50380 | Q688T8 | 2.1.2.1 | major CHO metabolism.synthesis.starch.AGPase | NA | NA | 7.99 | Oryza sativa mRNA for ADP glucose pyrophosphorylase large subunit, complete cds.|PLN |