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 |
|---|---|---|---|---|---|---|---|---|
Bra019240 | AT4G24230 | Q9STX1 | 35.1 | not assigned.annotated | -1.24 | 0.0074142 | 1 | sp|Q9STX1|ACBP3_ARATH Acyl-CoA-binding domain-containing protein 3 OS=Arabidopsis thaliana GN=ACBP3 PE=1 SV=1//2.64103e-67 |
Bra000480 | AT2G28840 | Q94B55 | 19.2.2.1.5.3.2 | .Protein homeostasis.ubiquitin-proteasome system.ubiquitin-fold protein conjugation.ubiquitin conjugation (ubiquitylation).ubiquitin-ligase E3 activities.RING-domain E3 ligase activities.RING-HC-class E3 ligase | -1.2302 | 0.0064297 | 1 | sp|Q94B55|XB31_ARATH Putative E3 ubiquitin-protein ligase XBAT31 OS=Arabidopsis thaliana GN=XBAT31 PE=2 SV=1//0 |
Bra027724 | AT1G64600 | 35.2 | not assigned.not annotated | -1.2284 | 0.0090418 | 1 | -//- | |
Bra008724 | AT5G15080 | 35.2 | not assigned.not annotated | -1.2255 | 0.015073 | 1 | -//- | |
Bra021614 | AT5G67360 | O65351 | 19.4.2.1.1 | .Protein homeostasis.proteolysis.serine-type peptidase activities.S8-class protease (subtilisin) families.protease (SBT1) | -1.2201 | 0.0028558 | 0.88179 | sp|O65351|SBT17_ARATH Subtilisin-like protease SBT1.7 OS=Arabidopsis thaliana GN=SBT1.7 PE=1 SV=1//0 |
Bra033869 | AT1G31880 | 35.1 | not assigned.annotated | -1.2186 | 0.016453 | 1 | -//- | |
Bra010780 | AT1G30280 | 22.1.6.4 | .Vesicle trafficking.clathrin coated vesicle (CCV) machinery.CCV accessory factors.clathrin uncoating protein (AUL) | -1.211 | 0.049505 | 1 | -//- | |
Bra031940 | AT5G64000 | O49623 | 27.5.5 | .Multi-process regulation.phosphoinositide lipid regulatory system.inositol polyphosphate 1-phosphatase | -1.2042 | 0.0038556 | 0.97824 | sp|O49623|DPNP2_ARATH SAL2 phosphatase OS=Arabidopsis thaliana GN=SAL2 PE=2 SV=1//0 |
Bra018039 | AT3G48740 | 24.2.6.1 | .Solute transport.carrier-mediated transport.TOC superfamily.sugar efflux transporter (SWEET) | -1.1993 | 0.0039098 | 0.98438 | -//- | |
Bra015085 | 35.2 | not assigned.not annotated | -1.1961 | 0.04317 | 1 | -//- | ||
Bra028220 | AT5G39000 | Q9FID8 | 11.10.2.4.2 | .Phytohormone action.signalling peptides.CRP (cysteine-rich-peptide) category.RALF/RALFL-peptide activity.RALF-peptide receptor (CrRLK1L) | -1.1956 | 0.026872 | 1 | sp|Q9FID8|Y5900_ARATH Putative receptor-like protein kinase At5g39000 OS=Arabidopsis thaliana GN=At5g39000 PE=3 SV=1//0 |
Bra021903 | AT2G34340 | 35.2 | not assigned.not annotated | -1.1929 | 0.016874 | 1 | -//- |