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Membrane proteome of euglenid plastid
Vanclová, Anna ; Hampl, Vladimír (advisor) ; Füssy, Zoltán (referee)
Euglenophyta are monophyletic group of euglenids defined by presence of green, three membrane- bound plastid which has been aquired via secondary endosymbiosis with chlorophyte alga. Mechanism of transport of nuclear-encoded proteins into this plastid is not yet completely understood. It was observed that the proteins are transported to the outermost plastid membrane in vesicles passing through ER and Golgi, but the mechanism of their recognition and fusion with the target membrane remains unclear. Translocation system of inner two membranes is still completely unknown, regarding the situation in other plastids, it has been proposed that homologues of TOC and TIC complexes are present. In this work we analyzed sequence data from proteome of isolated plastid membranes of model organism Euglena gracilis and transcriptome of E. gracilis and its distant relative Eutreptiella gymnastica. We studied whether they contain proteins potentially involved in transport and homologues of proteins of transport systems known from plastids in other organisms (TOC/TIC, ERAD-like transport, SNARE). However, all our results are negative. It is hard to determine whether these findings indicate the possible absence of TOC and TIC complexes in euglenid plastid, or rather the insufficiency of our data. Powered by TCPDF (www.tcpdf.org)
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Structure-function analysis of selected hop (Humulus lupulus L.) regulatory factors
FÜSSY, Zoltán
This work concentrated on isolation of novel hop transcription factors from bHLH, bZIP, MYB, and WRKY families involved in the regulation of lupulin flavonoid pathways, followed by their structural and functional analysis. Structural analyses included bioinformatic approaches to elucidate gene organization, domain structure of the putative protein products, and potential post-translational modifications. I performed site-directed mutagenesis to disclose the role of phosphorylation sites in HlbZIP1A stability. Further, this work determined protein-DNA interactions for obtained TFs, giving support to the binding of MYB-bHLH-WDR complexes to the promoter of chalcone synthase H1, a key enzyme of the lupulin flavonoid pathways. Employing bioinformatic approaches, quantitative RT-PCR and transient co-expression, I pointed out chalcone synthase H1 as a regulatory crossroads in the metabolic (flavonoid) responses during hop stunt viroid pathogenesis.
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Expression analysis of selected regulation factors in hop with relation to symptoms of viroid pathogenesis
FÜSSY, Zoltán
The aim of this work was to determine whether there are besides morphogenetic and metabolomic changes in viroid-infected plants also some alterations in the expression of transcription factors (TFs) known from our previous work to be involved in the secondary metabolites production, namely HlMyb1, HlMyb3, HlbHLH, HlbZIPA and HlbZIP2 TFs. Infectious vectors were prepared containing dimers of two closely related viroids- hop stunt viroid (HSVd) and cucumber pale fruit viroid (CPFVd). To achieve infection of hop (Humulus lupulus L.), biolistic inoculation of young shoots was performed. Hop cv. Admiral was chosen as a model for our experiments, because of its high flavonoid content in leaves. Infection of hop with both of these viroid species was proven by means of Northern hybridization and dot-blot techniques. Plants infected with HSVd showed serious symptoms such as stunted growth, epinasty and rugosity of leaves. Interestingly, decoloration of the petioles of the plants infected with HSVd was observed, maybe as a result of lower anthocyanins production. These symptoms were similar but milder in CPFVd-infected hops. On plants bearing symptoms, HPLC analyses were performed and compared to controls to detect changes in the levels of flavonol glycosides, phenolic acids, bitter acids and xanthohumol. In HSVd-infected hop leaves and petioles, significant decrease in the contents of flavonol glycosides and phenolic acids was observed. On the other hand, an increase in the amount of xanthohumol and bitter acids was detected in HSVd-infected tissues compared to healthy controls. Unlike to HSVd infection, the decrease of all analyzed secondary metabolites was observed in CPFVd-infected material. This difference suggests an alternative response of metabolome pathways to CPFVd-caused pathogenesis in comparison to HSVd. Semiquantitative RT PCR was performed to assay levels of TFs in healthy and infected hop tissues. Quantitative RealTime analyses of putative hop transcription factors HlbZIPA and HlbZIP2 were carried out using RNA isolated from HSVd-infected petioles. Increased mRNA levels of bZIP TFs were detected in infected material, suggesting an involvement of these factors in the response of the host plants to HSVd infection. Using thermodynamic methods of TGGE and heteroduplex analysis, several sequence variants of HlbZIP2 were idetified. According to aminoacid sequence alignment, this putative factor belongs to a group of bZIP proteins known for ABA/stress signalling in A. thaliana.
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