Hannover, University, Diss., 2005.

Hannover, University, Diss., 2004.

Marburg, Universiẗat, Diss., 2004.

No description available.

The Arbuscular mycorrhiza (AM) symbiosis is a mutual association formed by plant roots and soil fungi. Most vascular flowering plants have the ability to form AM associations, which show significant impact on ecosystem function and plant health. This association is based on the mutual exchange of nutrients between plant and fungus. Therefore, AM association leads to increased demands for photosynthesis. The main aim of this study was to investigate the pathway used by plants during AM to increase the photosynthetic performance. To achieve this aim, we used the model legume Medicago truncatula. We have found out that AM symbiosis develops in roots, where AM fungi colonize the roots, leading to better plant growth and more biomass. Furthermore, AM symbiosis increases chlorophyll content and photosynthetic electron transport rate in leaves. Based on these results we suggest that AM symbiosis increases both efficiency and capacity of photosynthetic apparatus in Medicago truncatula

This research investigated early transcriptional responses of the model legume, Medicago truncatula, to herbivory by caterpillars of the beet armyworm, Spodoptera exigua. Differentially expressed genes were identified by the differential display technique, cDNA-amplified fragment length polymorphism (cDNA-AFLP). To distinguish between caterpillar-specific responses and general wound responses, a subset of plants was mechanically damaged. Furthermore, to identify responses to salivary elicitors, plants were subject to herbivory by caterpillars with normal salivary secretions and those that had their spinneret, the appendage through which labial saliva is secreted, cauterized shut. Eighteen differentially expressed gene fragments, representing 16 genes, were identified. The expression pattern of 5 of these genes was analyzed by Northern analysis, confirming a caterpillar-specific reduction in transcripts encoding rubisco activase and glyceraldehyde-3-phosphate dehydrogenase. This research shows that plants are able to differentiate between caterpillar herbivory and mechanical damage and that transcriptional response are initiated within one hour after caterpillar infestation.

Arbuscular mycorrhizal (AM) fungi are a group of fungi that are able to establish a symbiotic relationship with the root system of many land plants. This symbiosis improves plant fitness by increasing the uptake of crucial mineral nutrients, particularly phosphorus and nitrogen. In return, the fungi receive organic carbon from the plant host in the form of sugars and lipids. The objective of my research is to assess whether the Nitrate and Peptide Transporter Family (NPF) of transport proteins play a role in mediating AM symbiosis. Firstly, we explored the involvement of NPF genes NPF1B and NPF4.12 by examining the phenotype of Medicago truncatula mutants. Secondly, we employed a modified yeast two-hybrid system to determine the phytohormone import capabilities of these NPF transport systems. Lastly, we employed reporter gene fusions to assess the spatial and temporal expression profiles of these NPF genes. The results of our research do not support our hypothesis that these NPF genes play a role in mediating AMF symbiosis. The results of the modified yeast-two hybrid tests revealed abscisic acid (ABA) and gibberellic acid (GA3) import capabilities of the transport system encoded by the gene NPF4.12. Future study of the diverse mechanisms that underpin AM symbiosis will nonetheless be useful to the agricultural industry by reducing farmer's reliance on chemical fertilizers.

Die Mykorrhiza (griechisch: mýkēs für „Pilz”; rhiza für „Wurzel”) stellt eine Symbiose zwischen Pilzen und einem Großteil der Landpflanzen dar. Der Pilz verbessert durch die Symbiose die Versorgung der Pflanze mit Nährstoffen, während die Pflanze den Pilz mit Kohlenhydraten versorgt. Die arbuskuläre Mykorrhiza (AM) stellt dabei einen beson-dere Form der Mykorrhiza dar. Der AM-Pilz bildet dabei während der Symbiose die namensgebenden Arbuskeln innerhalb der Wurzelzellen als Ort des primären Nährstoff- austausches aus. Die AM-Symbiose (AMS) ist der Forschungsschwerpunkt dieser Arbeit. Als Modellorganismen wurden Medicago truncatula und Glomus intraradices verwendet. Es wurden Transkriptionsanalysen durchgeführt um u.a. AMS regulierte Transkriptions- faktoren (TFs) zu identifizieren. Die Aktivität der Promotoren von drei der so identifizier-ten AMS-regulierten TFs (MtOFTN, MtNTS, MtDES) wurde mit Hilfe eine Reportergens visualisiert. Der Bereich der größten Promotoraktivität waren in einem Fall nur die ar- buskelhaltigen Zellen (MtOFTN). Im zweiten Fall war der Promotor auch aktiv in nicht arbuskelhaltigen Zellen, jedoch am stärksten aktiv in den arbuskelhaltigen Zellen (MtNTS). Ein weiterer Promotor war in arbuskelhaltigen Zellen und den diesen benach-barten Zellen gleich aktiv (MtDES). Zusätzlich wurden weitere Gene als AMS-reguliert identifiziert und es wurde für drei dieser Gene (MtPPK, MtAmT, MtMDRL) ebenfalls eine Promotor::Reporter-Aktivitäts- studie durchgeführt. Die Promotoren der Kinase (MtPPK) und des Ammoniumtrans-porters (MtAmt) waren dabei ausschließlich in arbuskelhaltigen Zellen aktiv, während die Aktivität des ABC-Transporters (MtMDRL) keinem bestimmten Zelltyp zuzuordnen war. Für zwei weitere identifizierte Gene, ein Kupfertransporter (MtCoT) und ein Zucker- bzw. Inositoltransporter (MtSuT), wurden RNA-Interferenz (RNAi)-Untersuchungen durchgeführt. Dabei stellte sich in beiden Fällen heraus, dass, sobald ein RNAi-Effekt in den transformierten Wurzeln vorlag, diese in einem deutlich geringerem Ausmaß wie in der Wurzelkontrolle von G. intraradices kolonisiert worden sind. Im Falle von MtCoT könnte das aus dem selben Grund geschehen, wie im Falle von MtPt4. Welche Rolle MtSuT genau in der Ausbildung der AMS spielt und welche Rolle Inositol in der Aus- bildung der AMS spielt müsste durch weitere Untersuchungen am Protein untersucht werden. Weitere Untersuchen an den in dieser Arbeit als spezifisch für arbuskelhaltige Zellen gezeigten Genen MtAmT, MtPPK und MtOFTN könnten ebenfalls aufschlussreich für das weitere Verständnis der AMS sein. Dies trifft auch auf die TFs MtNTS und MtDES zu, die zwar nicht ausschließlich arbuskelspezifisch transkribiert werden, aber auch eine Rolle in der Regulation der AMS innerhalb von M. truncatula Wurzeln zu spielen scheinen. / The mycorrhiza (Greek: mýkēs for "mushroom"; rhiza for "root") is a symbiosis between fungi and the vast majority of land plants. The fungus improves the nutrient supply of the plant, while the plant provides the fungus with carbohydrates. The arbuscular my-corrhiza (AM) represents a special type of mycorrhiza. The AM forms during the sym-biosis eponymous arbuscules within the root cells as the supposed site of the major nu-trient exchange. The AM symbiosis (AMS) is the research focus of this work. Medicago truncatula and Glomus intraradices were used as model organisms. During the project several transcription analysis were performed to identify AMS re-gulated transcription factors (TFs). The activity of the promoters of three of the identified AMS regulated TFs (MtOFTN, MtNTS, MtDES) were visualised using a reporter gene. Cells with promoter activity were in one case the arbuscle containing cells (MtOFTN). In the another case, the promoter was also weakly active in non arbuscle containing cells, however the major site of activity were the arbuscle containing cells (MtNTS). Another promoter was active in arbuscle containing and adjacent cells (MtDES). In addition, other genes were identified as AMS regulated and for three of these genes (MtPPK, MtAmT, MtMDRL) a promoter::reporter activity study was conducted, too. The promoters of the kinase (MtPPK) and the ammonium transporter (MtAmT) were active exclusively in arbuscle containing cells, whereas the activity of the ABC-transporter (MtMDRL) could not be assigned to a specific cell type. For two other identified genes (a copper transporter (MtCoT) and a sugar/ inositol transporter (MtSuT)) RNA-interference (RNAi) studies were carried out. The studies revealed in both cases that, once an RNAi effect was present in the transformed roots, the roots were colonised by G. intraradices in a much lesser extent as in the vector-control. In the case of MtCoT it maybe has the same basic principle as in the case of the phosphate transporter MtPt4. Which role MtSuT and inositol plays during the fo-rmation of the AMS has to be reviewed. Further examinations on the genes MtAmT, MtPPK and MtOFTN could also be reveal-ing for the understanding of the AMS, as their promotors, as shown in this thesis, are exclusively active in arbuscle containing cells The same can be said for the TFs MtNFTS and MtDES. They are not exclusively transcripted in arbuscle containing cells, but nevertheless seem to play a role in the formation of the AMS within M. truncatula roots.

L’interaction symbiotique légumineuses-rhizobium nécessite l'infection des racines de la plante par les bactéries et l’initiation de divisions cellulaires dans le cortex racinaire.Les cytokinines sont des hormones végétales agissant via une signalisation par phosphotransfert qui conduit à l’activation de Régulateurs de Réponse de type B (RRBs), des facteurs de transcription régulant l'expression des gènes de réponse primaire aux cytokinines. Une étude phylogénétique menée sur plusieurs espèces de légumineuses a révélé une expansion génique de la famille des RRBs et l’apparition de formes non-canoniques de ces facteurs de transcription. Chez Medicago truncatula,MtRRB3 est le RRB le plus fortement exprimé dans les racines et les nodosités et est impliqué dans la nodulation. En effet, les plantes dont l’expression de MtRRB3 a été réduite par ARNi ainsi que des mutants rrb3 présentent une diminution significative du nombre de nodosités formées. De plus, l’expression de gènes associés à la nodulation, tels que "Nodulation Signalling Pathway 2" (MtNSP2) et "Cell Cycle Switch 52A"(MtCCS52A), est réduite en réponse aux cytokinines dans ces mutants. Des fusions transcriptionnelles avec le rapporteur GUS montrent que MtRRB3, MtNSP2 et MtCCS52Aprésentent un profil d’expression spatiale largement chevauchant dans les racines et lesnodosités. Des expériences de ChIP-qPCR et de trans-activation en protoplastes indiquent par ailleurs que MtRRB3 peut respectivement interagir avec et activer les promoteurs des gènesMtNSP2 et MtCCS52A. Cette thèse a donc permis d’établir des mécanismes moléculaires impliqués dans les régulations transcriptionnelles médiées par les cytokinines lors de la mise en place des nodosités symbiotiques fixatrices d’azote. / The legume-rhizobium interaction requires the infection of plant roots by rhizobia and the initiation of cell divisions in the root cortex. Cytokinins, a class of plant hormones acts trough a phosphotranfert signalling leading to the activation of Type-B Response Regulators(RRBs) which are transcription factors regulating the expression of cytokinins primary response genes. Phylogenetic analyses carried out indifferent legume species genomes showed anexpansion of the RRB genes family associated toan increase in non-canonical RRBs. In Medicago truncatula nodules, MtRRB3 is the most expressed RRB in roots and nodules. MtRRB3 islinked to nodulation as MtRRB3 RNAi silencedplants as well as rrb3 mutants display asignificant decrease of nodule number. Inaddition, the expression of the nodulation related genes Nodulation Signalling Pathway 2(MtNSP2) and Cell Cycle Switch 52A(MtCCS52A) is reduced in response to cytokininsin rrb3 mutants. The expression pattern of apMtRRB3-GUS fusion overlaps with thepMtNSP2-GUS and pMtCCS52A-GUS fusions in roots and nodules. Finally, ChIP-qPCR and protoplast trans-activation experiments showed that MtRRB3 can respectively interacts with and activate MtNSP2 and MtCCS52A promoters. This thesis have thus established molecular mechanisms associated to transcriptional regulations mediated by cytokinins during the legume symbiotic nitrogen-fixing nodulation.

The study of root nodule symbiosis between nitrogen-fixing bacteria and leguminous plant species is important because of the ability to supplement fixed nitrogen fertilizers and increase plant growth in poor soils. Our group has isolated a mutant called nip in the model legume Medicago truncatula that is defective in nodule symbiosis. The nip mutant (numerous infections with polyphenolics) becomes infected by Sinorhizobium meliloti but then accumulates polyphenolic defense compounds in the nodule and fails to progress to a stage where nitrogen fixation can occur. Analysis of the transcriptome of nip roots prior to inoculation with rhizobia was undertaken using Affymetric Medicago Genome Array microarrays. The total RNA of 5-day old uninoculated seedlings was analyzed in triplicate to screen for the NIP gene based on downregulated transcript levels in the mutant as compared to wild type. Further microarray data was generated from 10 days post inoculation (dpi) nip and wild type plants. Analysis of the most highly downregulated transcripts revealed that the NIP gene was not identifiable based on transcript level. Putative gene function was assigned to transcripts with altered expression patterns in order to characterize the nip mutation phenotypically as inferred from the transcriptome. Functional analysis revealed a large number of chaperone proteins were highly expressed in the nip mutant, indicating high stress in the mutant prior to infection by rhizobia. Additionally, a database containing the information regarding the nip expression profile at both 0 days post inoculation (dpi) and 10 dpi were created for screening of candidate genes as predicted from sequence in the genomic region containing NIP.