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Hydrogen peroxide generated by over-expression of cytosolic superoxide dismutase in transgenic plums enhances bacterial canker resistance and modulates plant defence responses
H 2 O 2 generated during the oxidative burst, plays important roles in plant defenses responses against pathogens. In this study we examined the role of H 2 O 2 on bacterial canker resistance in transgenic plums over-expressing cytosolic superoxide dismutase. Three transgenic lines (C64, C66 and F12...
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Published in: | Molecular biology reports 2020-08, Vol.47 (8), p.5889-5901 |
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Main Authors: | , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | H
2
O
2
generated during the oxidative burst, plays important roles in plant defenses responses against pathogens. In this study we examined the role of H
2
O
2
on bacterial canker resistance in transgenic plums over-expressing cytosolic superoxide dismutase. Three transgenic lines (C64, C66 and F12) with elevated levels of H
2
O
2
accumulation showed enhanced resistance against bacterial canker disease caused by
Pseudomonas syringae
pv.
syringae
, when compared to the non-transformed control. Analysis of the expression of several genes involved in the plant–pathogen interaction showed that the expression of those involved in SA pathway (
pr1
and
npr1
) and JA (
lox3
) were activated earlier and transiently in transgenic lines C66 and F12 when compared to the wild type. However, the expression of genes involved in anthocyanin synthesis (
chi
,
chs, f3h
,
dfr, atcs, myb10
) and ethylene (
acs
) was induced at very low levels whereas it was activated by the pathogen at exaggerated levels in the non-transformed line. These results suggest that resistance observed in transgenic lines over-producing H
2
O
2
is correlated with an early and transient induction of defense genes associated with the SA and JA pathways and inhibition of gene expression associated with ethylene and anthocyanin biosynthesis. |
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ISSN: | 0301-4851 1573-4978 |
DOI: | 10.1007/s11033-020-05660-8 |