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Species & Dataset

Experiment

Foliar Ozone Injury

  • Oryza sativa

  • Common name: Asian rice

  • Family: Poaceae

  • Cultivar: cv. Nipponbare; O. sativa L. japonica-type

  • Tissue: Third and fourth leaves of 2-week old rice plant

  • Ozone concentration: ​ 0.2 ppm

  • Ozone exposure: 24 hours

  • Sampling time: ​ 0, 6, 12 and 24 hrs after ozone treatment

  • Platform: DNA Microarray

  • Year of study: 2008

  • Location: Japan

Injury Rice.jpeg

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.

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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
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