ROS1-Dependent DNA Demethylation Is Required for ABA-Inducible NIC3 Expression
DNA methylation plays an important role in diverse developmental processes in many eukaryotes, including the response to environmental stress. Abscisic acid (ABA) is a plant hormone that is up-regulated under stress. The involvement of DNA methylation in the ABA response has been reported but is poo...
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Veröffentlicht in: | Plant physiology (Bethesda) 2019-04, Vol.179 (4), p.1810-1821 |
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Sprache: | eng |
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Zusammenfassung: | DNA methylation plays an important role in diverse developmental processes in many eukaryotes, including the response to environmental stress. Abscisic acid (ABA) is a plant hormone that is up-regulated under stress. The involvement of DNA methylation in the ABA response has been reported but is poorly understood. DNA demethylation is a reverse process of DNA methylation and often induces structural changes of chromatin leading to transcriptional activation. In Arabidopsis (
, active DNA demethylation depends on the activity of REPRESSOR OF SILENCING 1 (ROS1), which directly excises 5-methylcytosine from DNA. Here we showed that
mutants were hypersensitive to ABA during early seedling development and root elongation. Expression levels of some ABA-inducible genes were decreased in
mutants, and more than 60% of their proximal regions became hypermethylated, indicating that a subset of ABA-inducible genes are under the regulation of ROS1-dependent DNA demethylation. Notable among them is
(
) that encodes an enzyme that converts nicotinamide to nicotinic acid in the NAD
salvage pathway. Many enzymes in this pathway are known to be involved in stress responses. The
mutants display hypersensitivity to ABA, whereas overexpression of
restores normal ABA responses. Our data suggest that
is responsive to ABA but requires ROS1-mediated DNA demethylation at the promoter as a prerequisite to transcriptional activation. These findings suggest that ROS1-induced active DNA demethylation maintains the active state of
transcription in response to ABA. |
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ISSN: | 0032-0889 1532-2548 |
DOI: | 10.1104/pp.18.01471 |