Blue light suppression alters cytokinin homeostasis in wheat leaves senescing under shading stress
Language English Country France Media print-electronic
Document type Journal Article
PubMed
30142601
DOI
10.1016/j.plaphy.2018.08.005
PII: S0981-9428(18)30343-7
Knihovny.cz E-resources
- Keywords
- Blue light, Cytokinin metabolism, Gene expression, Leaf senescence, Shading stress, Triticum aestivum,
- MeSH
- Chlorophyll metabolism MeSH
- Cytokinins metabolism MeSH
- Phylogeny MeSH
- Homeostasis radiation effects MeSH
- Real-Time Polymerase Chain Reaction MeSH
- Plant Leaves metabolism radiation effects MeSH
- Oxidoreductases metabolism MeSH
- Triticum metabolism radiation effects MeSH
- Gene Expression Regulation, Plant radiation effects MeSH
- Genes, Plant genetics MeSH
- Plant Proteins metabolism MeSH
- Light MeSH
- Transcriptome MeSH
- Publication type
- Journal Article MeSH
- Names of Substances
- Chlorophyll MeSH
- cytokinin oxidase MeSH Browser
- Cytokinins MeSH
- Oxidoreductases MeSH
- Plant Proteins MeSH
Blue light (BL) suppression accelerates the senescence rate of wheat (Triticum aestivum L.) leaves exposed to shading. In order to study whether this effect involves the alteration of different cytokinin (CK) metabolites, CK-degradation, as well as the expression profile of genes responsible of CK-perception, -inactivation, -reactivation and/or -turnover, leaf segments of 30 day-old plants were placed in boxes containing bi-distilled water and covered with blue (B) or green (G) light filters, which supplied a similar irradiance but differed in the percentage of BL transmitted (G << B). A neutral (N) filter was used as control. When appropriate, different CK metabolites or an inhibitor of CK-degradation were added in order to alter the endogenous CK levels. A rapid decrement of trans-zeatin (tZ) and cis-zeatin (cZ) content was observed after leaf excision, which progressed at a higher rate in treatment G than in the control and B treatments. Senescence progression correlated with an accumulation of glycosylated forms (particularly cZ-derivatives), and an increment of CK-degradation, both of which were slowed in the presence of BL. On the contrary, CK-reactivation (analyzed through TaGLU1-3 expression) was delayed in the absence of BL. When different CK were exogenously supplied, tZ was the only natural free base capable to emulate the senescence-retarding effect of BL. Even though the signaling components involved in the regulation of senescence rate and CK-homeostasis by BL remain elusive, our data suggest that changes in the expression profile and/or functioning of the transcription factor HY5 might play an important role.
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