Species & Dataset
Experiment
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Brassica campestris
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Common name: Mustard, Pak choi
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Family: Brassicaceae
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Cultivar: Pak Choi (‘Jingguan’)
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Tissue: Second leaves from the top
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Ozone concentration: 251.71 ± 8.15 ppb
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Ozone exposure: 2 days (8 hours/day)
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Sampling time: End of exposure period
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Platform: Illumina Hiseq 2500
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Year of study: 2017
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Location: China
Title: Transcriptomic analysis of Pak Choi under acute ozone exposure revealed regulatory mechanism against ozone stress
Summary: Ground-level ozone (O3) is one of the major air pollutants, which cause oxidative injury to plants. The physiological and biochemical mechanisms underlying the responses of plants to O3 stress have been well investigated. However, there are limited reports about the molecular basis of plant responses to O3. In this study, a comparative transcriptomic analysis of Pak Choi (Brassica campestris ssp. chinensis) exposed to different O3 concentrations was conducted for the first time. Seedlings of Pak Choi with five leaves were exposed to non-filtered air (NF, 31 ppb) or elevated O3 (E-O3, 252 ppb) for 2 days (8 h per day, from 9:00–17:00). Compared with plants in the NF, a total of 675 differentially expressed genes (DEGs) were identified in plants under E-O3, including 219 DEGs with decreasedexpressions and 456 DEGs with increased expressions. Kyoto Encyclopedia of Genes and Genomes (KEGG) analyses revealed that O3 stress invoked multiple cellular defense pathways to mitigate the impaired cellular integrity and metabolism, including ‘glutathione metabolism’, ‘phenylpropanoid biosynthesis’, ‘sulfur metabolism’, ‘glucosinolate biosynthesis’, ‘cutin, suberine and wax biosynthesis’ and others. Transcription factors potentially involved in this cellular regulation were also found, such as AP2-ERF, WRKY, JAZ, MYB etc. Based on the RNA-Seq data and previous studies, a working model was proposed integrating O3 caused reactive oxygen burst, oxidation-reduction regulation, jasmonic acid and downstream functional genes for the regulation of cellular homeostasis after acute O3 stress. The present results provide a valuable insight into the molecular responses of Pak Choi to acute O3 stress and the specific DEGs revealed in this study could be used for further functional identification of key allelic genes determining the O3 sensitivity of Pak Choi.
Data repository: NCBI Sequence Read Archive (SRA) repository (Accession number SRP100739)
Reference: Zhang, L., Xu, B., Wu, T., Wen, M.X., Fan, L.X., Feng, Z.Z. and Paoletti, E., 2017. Transcriptomic analysis of Pak Choi under acute ozone exposure revealed regulatory mechanism against ozone stress. BMC plant biology, 17(1), pp.1-15.
Gene Identifier | AGI Gene Code | Uniprot ID | Bin Code | Bin Name | log2FC | p-value | FDR adjusted p-value | Functional annotation |
|---|---|---|---|---|---|---|---|---|
Bra005688 | AT5G01380 | Q9SDW0 | 15.5.20 | .RNA biosynthesis.transcriptional regulation.transcription factor (Trihelix) | 3.9547 | 0.0000798 | 0.10499 | sp|Q9SDW0|TGT3A_ARATH Trihelix transcription factor GT-3a OS=Arabidopsis thaliana GN=GT-3A PE=1 SV=1//4.82249e-125 |
Bra002400 | AT5G22250 | 16.8.2.1.2.2 | .RNA processing.RNA surveillance.mRNA deadenylation-dependent decay.mRNA deadenylation.CCR4-NOT complex.deadenylase component CAF1 | 3.9702 | 0.01972 | 1 | -//- | |
Bra018969 | Q9SE50 | 50.3.2 | .Enzyme classification.EC_3 hydrolases.EC_3.2 glycosylase | 3.9712 | 9.1e-10 | 0.0000149 | sp|Q9SE50|BGL18_ARATH Beta-D-glucopyranosyl abscisate beta-glucosidase OS=Arabidopsis thaliana GN=BGLU18 PE=1 SV=2//0 | |
Bra029307 | AT5G61820 | 35.2 | not assigned.not annotated | 3.982 | 0.03564 | 1 | -//- | |
Bra035973 | AT1G05440 | 35.2 | not assigned.not annotated | 3.9977 | 0.047185 | 1 | -//- | |
Bra006964 | 50.1.1 | .Enzyme classification.EC_1 oxidoreductases.EC_1.1 oxidoreductase acting on CH-OH group of donor | 4.0023 | 0.0043738 | 1 | -//- | ||
Bra005939 | 50.1.8 | .Enzyme classification.EC_1 oxidoreductases.EC_1.8 oxidoreductase acting on sulfur group of donor | 4.0357 | 0.03096 | 1 | -//- | ||
Bra023689 | AT5G18620 | 12.4.1.1.4 | .Chromatin organisation.chromatin remodeling complexes.ATPase modules.Snf2-like group.chromatin remodeling factor (Iswi) | 4.0796 | 0.016404 | 1 | -//- | |
Bra023394 | AT5G13170 | Q9FY94 | 24.2.6.1 | .Solute transport.carrier-mediated transport.TOC superfamily.sugar efflux transporter (SWEET) | 4.1139 | 0.014122 | 1 | sp|Q9FY94|SWT15_ARATH Bidirectional sugar transporter SWEET15 OS=Arabidopsis thaliana GN=SWEET15 PE=2 SV=1//1.90673e-159 |
Bra019777 | AT1G12610 | 15.5.7.2 | .RNA biosynthesis.transcriptional regulation.AP2/ERF transcription factor superfamily.transcription factor (DREB) | 4.1268 | 0.019374 | 1 | -//- | |
Bra039984 | AT2G29480 | Q9ZW29 | 18.8.1.4 | .Protein modification.S-glutathionylation.glutathione S-transferase activities.class tau glutathione S-transferase | 4.166 | 0.0039897 | 0.98925 | sp|Q9ZW29|GSTU2_ARATH Glutathione S-transferase U2 OS=Arabidopsis thaliana GN=GSTU2 PE=2 SV=1//9.34868e-142 |
Novel01116 | #N/A | #N/A | 4.2131 | 0.00025504 | 0.19908 | BnaC04g24690D [Brassica napus] |