2020
DOI: 10.1134/s1021443720050192
|View full text |Cite
|
Sign up to set email alerts
|

Participation of Jasmonate Signaling Components in the Development of Arabidopsis thaliana’s Salt Resistance Induced by H2S and NO Donors

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1

Citation Types

1
4
0

Year Published

2021
2021
2024
2024

Publication Types

Select...
5
2

Relationship

1
6

Authors

Journals

citations
Cited by 11 publications
(5 citation statements)
references
References 25 publications
1
4
0
Order By: Relevance
“…The SOD activity in control in jin1 plants was lower than in wild-type and coi1 genotype plants (Fig. 2, A), which is apparently due to genetics and is consistent with the results obtained in other series of experiments [27]. Incubation of plants of all three studied genotypes on a medium with 150 mM NaCl caused a decrease in SOD activity (Fig.…”
Section: Resultssupporting
confidence: 91%
See 2 more Smart Citations
“…The SOD activity in control in jin1 plants was lower than in wild-type and coi1 genotype plants (Fig. 2, A), which is apparently due to genetics and is consistent with the results obtained in other series of experiments [27]. Incubation of plants of all three studied genotypes on a medium with 150 mM NaCl caused a decrease in SOD activity (Fig.…”
Section: Resultssupporting
confidence: 91%
“…Based on the data obtained by bioinformatics methods, it was concluded that the MYC family genes are involved in the transduction of NO signals [26]. Our data on an increase in the salt resistance of Arabidopsis wildtype plants under the influence of NO and H 2 S donors and a very weak manifestation of such effects in mutants jin1 and coi1, defective in jasmonate signaling, indicates the involvement of components of this signaling in the implementation of stressprotective effects of gasotransmitters NO and H 2 S [27]. In gene ral, jasmonic acid and its derivatives are considered as one of the important links in plant adaptation to abiotic and biotic stress factors [28,29].…”
mentioning
confidence: 60%
See 1 more Smart Citation
“…The effect of exogenous hydrogen sulfide on the salt tolerance of plants can be phenomenologically similar to the effects of NO donors. Hence, NO and H 2 S donors had a similar positive effect on the salt tolerance of wild-type Arabidopsis plants, which was manifested in a decrease, under their influence, of water deficit in leaves, a decrease in oxidative damage, stabilization of membrane permeability, and chlorophyll content under the action of 175 mM NaCl [217]. Also, under the influence of NaHS and SNP treatment during salinity in Col-0 plants, the activity of antioxidant enzymes increased, but the stressinduced accumulation of proline declined.…”
Section: High Salinitymentioning
confidence: 86%
“…H 2 S at low concentrations regulates seed germination (Baudouin et al, 2016;Li, 2020), root growth (Hu et al, 2020), stomatal apertures (Lisjak et al, 2011;, flower senescence (Huo et al, 2018), photosynthesis (Chen et al, 2011), autophagy (Alvarez, Garcia, Moreno, et al, 2012;Laureano-Marin et al, 2016;Romero et al, 2014), and biotic and abiotic stress tolerance (Hancock & Whiteman, 2014;Kaya, Higgs, et al, 2020;Li, 2013;Shi et al, 2015;Zulfiqar & Hancock, 2020). This molecule has been known to alleviate various abiotic stresses, for example, heavy metal (Ahmad et al, 2020;Fang et al, 2016;Li, Shah, et al, 2021;Li, Wang, & Shen, 2012;Luo et al, 2020;Ozfidan-Konakci et al, 2020;Shen et al, 2013;Zhang, Hu, et al, 2008), drought (Shen et al, 2013), water logging (Xiao et al, 2020), high temperature (Li, Gong, et al, 2012), low temperature (Liu et al, 2020;Nasibi et al, 2020;Tang et al, 2020) salinity (Ding et al, 2019;Ma et al, 2018;Shi et al, 2013;Yastreb, et al 2020), and alkalinity (Bahmanbiglo & Eshghi, 2021;Dawood et al, 2021). It is produced endogenously within plants, suggesting its role as a signaling molecule (Fuentes-Lara et al, 2019;Li, 2013;Zhang et al, 2021).…”
mentioning
confidence: 99%