Imbalance in expression of hop (Humulus lupulus) chalcone synthase H1 and its regulators during hop stunt viroid pathogenesis
Jazyk angličtina Země Německo Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
23395540
DOI
10.1016/j.jplph.2012.12.006
PII: S0176-1617(13)00020-5
Knihovny.cz E-zdroje
- MeSH
- acyltransferasy genetika metabolismus MeSH
- down regulace MeSH
- exprese genu MeSH
- Humulus enzymologie genetika virologie MeSH
- listy rostlin enzymologie genetika virologie MeSH
- messenger RNA chemie genetika MeSH
- nemoci rostlin virologie MeSH
- polymerázová řetězová reakce s reverzní transkripcí MeSH
- propanoly metabolismus MeSH
- regulace genové exprese enzymů * MeSH
- regulace genové exprese u rostlin MeSH
- RNA interference MeSH
- RNA rostlin chemie genetika MeSH
- RNA virová chemie genetika MeSH
- rostlinné proteiny genetika metabolismus MeSH
- stonky rostlin enzymologie genetika virologie MeSH
- transkripční faktory genetika metabolismus MeSH
- upregulace MeSH
- viroidy patogenita fyziologie MeSH
- výpočetní biologie MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- 1-phenylpropanol MeSH Prohlížeč
- acyltransferasy MeSH
- flavanone synthetase MeSH Prohlížeč
- messenger RNA MeSH
- propanoly MeSH
- RNA rostlin MeSH
- RNA virová MeSH
- rostlinné proteiny MeSH
- transkripční faktory MeSH
Viroid-derived small RNAs generated during hop stunt viroid (HSVd) pathogenesis may induce the symptoms found in the hop cultivar "Admiral", including observed shifts in phenylpropanoid metabolites and changes in petiole coloration. Using quantitative RT-PCR, we examined hop lupulin gland-specific genes that have been shown to be involved in phenylpropanoid metabolism, for altered expression in response to infection with two HSVd isolates, HSVd-g and CPFVd. Most notably, the expression of a gene encoding a key enzyme for phenylpropanoid synthesis, naringenin-chalcone synthase H1 (chs_H1), decreased up to 40-fold in infected samples. In addition, a marked decrease in the expression of HlbHLH2 and an increase in the expression of HlMyb3 were observed. These two genes encode transcription factors that form a ternary complex with HlWDR1 for chs_H1 promoter activation. In a transient expression assay, a decrease in the ternary complex potential to activate the chs_H1 promoter was observed upon the decrease of HlbHLH2 expression. In addition, targeting of the chs_H1 transcript by vd-sRNAs may contribute to these expression changes. Our data show that HSVd infection causes a significant imbalance in the expression of phenylpropanoid metabolite-affecting genes via a complex mechanism, possibly involving regulatory disorders and direct targeting by vd-sRNA.
University of South Bohemia Faculty of Science Branišovská 31 370 05 České Budějovice Czech Republic
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