Involvement of putrescine in osmotic stress-induced ABA signaling in leaves of wheat seedlings

To elucidate one mechanism by which putrescine (Put) functions in plant signaling under osmotic stress, Put and ABA contents, and plasma membrane-NADPH oxidase (PM-NOX) activity were detected in wheat seedling leaves. Under osmotic stress, ABA and Put contents, PM-NOX activity, and PM-NOX-dependent...

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Veröffentlicht in:Journal of biosciences 2019-12, Vol.44 (6), p.1-6, Article 136
Hauptverfasser: Du, HY, Chen, GS, Yu, JM, Bao, YY, Liu, GT, Liu, HP, Gupta, R
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Sprache:eng
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Zusammenfassung:To elucidate one mechanism by which putrescine (Put) functions in plant signaling under osmotic stress, Put and ABA contents, and plasma membrane-NADPH oxidase (PM-NOX) activity were detected in wheat seedling leaves. Under osmotic stress, ABA and Put contents, PM-NOX activity, and PM-NOX-dependent O 2 .− production all increased. The inhibitor tungstate (T) of ABA bio-synthesis reduced the increases in ABA and Put contents under osmotic stress. The inhibitor D-arginine (D-Arg) of Put bio-synthesis didn’t reduce osmotic-induced increase of ABA, but it inhibited the increases of PM-NOX activity and O 2 . − production, and the inhibitory effects were reversed by exogenous Put. These findings suggested that ABA might regulate Put biosynthesis, and Put might regulate PM-NOX activity. Treatments with three inhibitors imidazole (I), diphenylene iodonium (DPI) and pyridine (P) of PM-NOX reduced significantly not only O 2 . − production, but also the stress-induced increase of Put content, which indicated that O 2 . − production might regulate Put biosynthesis. Treatments with EGTA (Ca 2+ chelator), La 3+ and verapamil (V) (Ca 2+ channel blockers) reduced significantly the stress-induced increase of Put content, which suggested that Ca 2+ might regulate Put biosynthesis. With these findings, it could be concluded that Put was involved in ABA signaling induced by osmotic stress via regulating PM-NOX activity in wheat seedling leaves.
ISSN:0250-5991
0973-7138
DOI:10.1007/s12038-019-9949-4