top of page
Species & Dataset
Experiment
Foliar ozone injury
  • Arabidopsis thaliana

  • Common name: Thale cress, Mouse-ear cress

  • Family: Brassicaceae

  • Cultivar: Col-0 (wild type), ein2 (Ethylene signaling deficient), sid2 (Salicylic acid biosynthesis deficient)

  • Tissue: Rosettes

  • Ozone concentration: 200 nL L-1

  • Ozone exposure: 24 hours

  • Platform: Macroarray

  • Year of study: 2009

  • Location: Japan

Arabidopsis_injury.png

Title:  Ethylene and salicylic acid control glutathione biosynthesis in ozone-exposed Arabidopsis thaliana.

Summary: Ozone produces reactive oxygen species and induces the synthesis of phytohormones, including ethylene and salicylic acid. These phytohormones act as signal molecules that enhance cell death in response to ozone exposure. However, some studies have shown that ethylene and salicylic acid can instead decrease the magnitude of ozone-induced cell death. Therefore, we studied the defensive roles of ethylene and salicylic acid against ozone.Unlike the wild-type, Col-0, Arabidopsis mutants deficient in ethylene signaling (ein2) or salicylic acid biosynthesis (sid2) generated high levels of superoxide and exhibited visible leaf injury, indicating that ethylene and salicylic acid can reduce ozone damage. Macroarray analysis suggested that the ethylene and salicylic acid defects influenced glutathione (GSH) metabolism. Increases in the reduced form of GSH occurred in Col-0 6 h after ozone exposure, but little GSH was detected in ein2 and sid2 mutants, suggesting that GSH levels were affected by ethylene or salicylic acid signaling. We performed gene expression analysis by real-time polymerase chain reaction using genes involved in GSH metabolism. Induction of γ-glutamylcysteine synthetase (GSH1), glutathione synthetase (GSH2), and glutathione reductase 1 (GR1) expression occurred normally in Col-0, but at much lower levels in ein2 and sid2. Enzymatic activities of GSH1 and GSH2 in ein2 and sid2 were significantly lower than in Col-0. Moreover, ozone-induced leaf damage observed in ein2 and sid2 was mitigated by artificial elevation of GSH content. Our results suggest that ethylene and salicylic acid protect against ozone-induced leaf injury by increasing de novo biosynthesis of GSH.

Reference: Yoshida, S., Tamaoki, M., Ioki, M., Ogawa, D., Sato, Y., Aono, M., Kubo, A., Saji, S., Saji, H., Satoh, S. and Nakajima, N., 2009. Ethylene and salicylic acid control glutathione biosynthesis in ozone‐exposed Arabidopsis thaliana. Physiologia Plantarum, 136(3), pp.284-298.

sid2

ein2

Col-0

AGI Gene Code
Uniprot ID
Bin Code
Bin Name
Col-0 (0 h)
Col-0 (3 h)
Col-0 (6 h)
Col-0 (12 h)
ein2 (0 h)
ein2 (3 h)
ein2 (6 h)
ein2 (12 h)
sid2 (0 h)
sid2 (3 h)
sid2 (6 h)
sid2 (12 h)
Functional annotation
Gene
AT1G07940
P0DH99
29.2.4
protein.synthesis.elongation
1
1
1
1
1
1
1
1
1
1
1
1
Elongation factor 1-alpha
EF-1?
AT2G01010
#N/A
29.2.6
protein.synthesis.ribosomal RNA
0.72
0.87
0.76
0.47
0.77
0.79
0.64
0.53
0.6
0.78
0.55
0.5
18S rRNA
18SrRNA
AT5G44340
P24636
31.1
cell.organisation
0.69
1.19
0.83
0.58
0.57
0.74
0.92
0.69
0.54
0.62
0.65
0.52
Tubulin beta-4 chain
TUBULIN4
AT1G49240
Q96293
31.1
cell.organisation
0.75
1.21
0.67
0.48
0.53
0.75
0.57
0.58
0.52
0.8
0.64
0.49
Actin 8
ACTIN8
AT1G55020
Q06327
17.7.1.2
hormone metabolism.jasmonate.synthesis-degradation.lipoxygenase
0.22
0.39
0.35
0.23
0.16
0.32
0.27
0.4
0.11
0.14
0.27
0.23
Lipoxygenase 1
LOX1
AT3G45140
P38418
17.7.1.2
hormone metabolism.jasmonate.synthesis-degradation.lipoxygenase
0.64
1.37
2.34
1.49
0.53
1.53
1.79
1.5
0.28
1.23
1.73
1.27
Lipoxygenase 2
LOX2
AT5G42650
Q96242
17.7.1.3
hormone metabolism.jasmonate.synthesis-degradation.allene oxidase synthase
0.65
1.23
0.82
0.38
0.41
1
0.91
0.58
0.4
1.02
0.9
0.63
Allene oxide synthase
AOS
AT3G16470
O04309
17.7.3
hormone metabolism.jasmonate.induced-regulated-responsive-activated
0.63
1.67
1.76
0.77
0.37
1.21
1.51
0.93
0.38
1.05
1.25
0.81
JA-responsive gene
JIP?JR?
AT5G52310
Q06738
20.2.2
stress.abiotic.cold
0.28
0.6
0.39
0.19
0.24
0.39
0.42
0.28
0.19
0.29
0.33
0.37
Desiccation-responsive protein 29A
RD29A
AT5G25610
Q08298
20.2.3
stress.abiotic.drought/salt
3.04
2.3
1.57
1.16
1.78
1.75
1.12
0.95
2.23
1.55
1.19
1.43
Dehydration-responsive protein 22
RD22
AT5G15970
P31169
31.1
cell.organisation
0.78
1.3
1.47
0.53
0.55
1.03
1.25
0.67
0.36
0.74
1.25
0.7
Cold-responsive 6.6
KIN2
AT1G20440
P31168
20.2.99
stress.abiotic.unspecified
0.63
0.94
0.8
0.41
0.48
0.39
0.76
0.48
0.31
0.49
0.74
0.55
Cold regulated 47
COR47
bottom of page