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Carbon Catabolism in <i>Bacillus subtilis</i>: Global and Molecular Views on the Control of Gene Expression / Kohlenstoffmetabolismus in <i>Bacillus subtilis</i>: Globale und Molekulare Sicht auf die Kontrolle der GenexpressionSchilling, Oliver 05 July 2007 (has links)
No description available.
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Quantifying the Life Stages of a Biomolecule: Implications for the Circadian TranscriptomeLück, Sarah 05 December 2017 (has links)
Viele biologische Prozesse im Verhalten von ganzen Organismen, aber auch in den Prozessen und
der biochemischen Zusammensetzung von Zellen zeigen einen zirkadianen Rhythmus, also einen Rhythmus mit einer Periode von etwa 24 Stunden.
Diese 24-Stunden-Rhythmen sind in der Genexpression auf allen Ebenen zu finden: von der Tran-
skriptionsinitiation bis zur Proteindegradation. Auf Transkriptebene, zirkadiane mRNA-Produktion
und mRNA-Abundanz ist umfassend gemessen. Auf der anderen Seite, zirkadiane posttranskriptionelle Regulation ist weit weniger verstanden. In dieser Arbeit untersuche ich, wie bisher ungemessene, posttranskriptionelle Prozesse die rhythmischen Eigenschaften der Genexpression beeinflussen. Dazu beschreibe ich die Lebensstadien eines Bio-Moleküls mit einem Modell-Motiv, einer einfachen Differentialgleichung mit zeitabhängigen, rhythmischen Raten.
Als erstes diskutiere ich die Einschränkungen von Phase und Amplitude zirkadianer Transkripte, die nur von konstanter PTR beeinflusst werden. Bei vielen gemessenen Transkripten sind diese Einschränkungen verletzt. In diesen Fällen muss es eine rhythmische PTR geben. Ich untersuche, welche rhythmische PTR diese Fälle erklären können und führe einen statistischen Test ein, der auf unbeobachtete, rhythmische PTR testet. Durch die Analyse zweier Datensätze von Mausleber und -niere finde ich, dass 18% aller zirkadianen Gene in Niere und 34% in Leber rhythmisch
posttranskriptionell reguliert sind.
Im zweiten Teil analysiere ich weitere Aspekte von PTR in einem Hypothesen-getriebenen Ansatz.
Ich zeige, dass Spleißen mit einem Rhythmus von 24 Stunden 12 Stunden-Rhythmen in der Abundanz von mRNA erzeugen kann. Als nächstes schlage ich ein Modell vor, das rhythmische Degradation von Mitgliedern der zirkadianen Uhr beschreibt. Schließlich erweitere ich das Modell-Grundmotiv zu einer partiellen Differentialgleichung (PDG), die das “Altern” von Molekülen beschreibt. / In almost all organisms on Earth, many behavioral, physiological, and biochemical activities
oscillate with a circadian rhythm, a rhythm with a period of about 24 hours.
In gene expression, the 24-hour-rhythm can be found on all stages: from transcription initiation
to protein degradation. On the transcript level, circadian mRNA production and mRNA abundance
are comprehensively charted through numerous genome-wide high throughput studies. Circadian post-transcriptional regulation, however, is less well understood. In this thesis, I will investigate how unobserved post-transcriptional processes influence rhythmic properties of gene expression. To this end, I quantify the life-stages of biomolecules using one modeling motif, a simple ordinary differential equation describing production and degradation with time-dependent rhythmic rates. This basic modeling motif is systematically varied to examine and discuss various influences of post-transcriptional regulation (PTR) on circadian mRNA expression.
I first discuss the restrictions of rhythmic phase and amplitude of circadian transcripts influenced by non-rhythmic PTR. For many genes these restrictions are violated and we have to assume the existence of a rhythmic PTR. I discuss which rhythmic PTR can explain these findings and further introduce a statistical test to quantify the extent of unobserved rhythmic PTR. Analyzing two data sets on mouse liver and kidney, I find that 18% of circadian genes in kidney and 34% in liver are under rhythmic post-transcriptional control.
In a second part, I analyze more specific aspects of PTR in a hypothesis-driven approach. Firstly,
I find that splicing with a rhythm of 24 hours is able to generate 12-hour rhythms in abundance
of mature mRNA. Secondly, I propose and analyze a model to investigate rhythmic degradation of core clock genes. And finally, I extend the core modeling motif to a partial differential equation (PDE) model that accounts for the “aging” process of molecules.
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Verticillium longisporum induced gene expression in Arabidopsis thaliana / Verticillium longisporum induzierte Genexpression in Arabidopsis thalianaTappe, Hella 28 April 2008 (has links)
No description available.
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Transport processes in the arbuscular mycorrhizal symbiosisDuensing, Nina January 2013 (has links)
The nutrient exchange between plant and fungus is the key element of the arbuscular mycorrhizal (AM) symbiosis. The fungus improves the plant’s uptake of mineral nutrients, mainly phosphate, and water, while the plant provides the fungus with photosynthetically assimilated carbohydrates. Still, the knowledge about the mechanisms of the nutrient exchange between the symbiotic partners is very limited. Therefore, transport processes of both, the plant and the fungal partner, are investigated in this study. In order to enhance the understanding of the molecular basis underlying this tight interaction between the roots of Medicago truncatula and the AM fungus Rhizophagus irregularis, genes involved in transport processes of both symbiotic partners are analysed here.
The AM-specific regulation and cell-specific expression of potential transporter genes of M. truncatula that were found to be specifically regulated in arbuscule-containing cells and in non-arbusculated cells of mycorrhizal roots was confirmed. A model for the carbon allocation in mycorrhizal roots is suggested, in which carbohydrates are mobilized in non-arbusculated cells and symplastically provided to the arbuscule-containing cells. New insights into the mechanisms of the carbohydrate allocation were gained by the analysis of hexose/H+ symporter MtHxt1 which is regulated in distinct cells of mycorrhizal roots. Metabolite profiling of leaves and roots of a knock-out mutant, hxt1, showed that it indeed does have an impact on the carbohydrate balance in the course of the symbiosis throughout the whole plant, and on the interaction with the fungal partner. The primary metabolite profile of M. truncatula was shown to be altered significantly in response to mycorrhizal colonization.
Additionally, molecular mechanisms determining the progress of the interaction in the fungal partner of the AM symbiosis were investigated. The R. irregularis transcriptome in planta and in extraradical tissues gave new insight into genes that are differentially expressed in these two fungal tissues. Over 3200 fungal transcripts with a significantly altered expression level in laser capture microdissection-collected arbuscules compared to extraradical tissues were identified. Among them, six previously unknown specifically regulated potential transporter genes were found. These are likely to play a role in the nutrient exchange between plant and fungus. While the substrates of three potential MFS transporters are as yet unknown, two potential sugar transporters are might play a role in the carbohydrate flow towards the fungal partner.
In summary, this study provides new insights into transport processes between plant and fungus in the course of the AM symbiosis, analysing M. truncatula on the transcript and metabolite level, and provides a dataset of the R. irregularis transcriptome in planta, providing a high amount of new information for future works. / In der arbuskulären Mykorrhiza (AM) Symbiose werden die Wurzeln fast aller Landpflanzen von Pilzen der Abteilung Glomeromycota besiedelt. Der Pilz erleichtert der Pflanze die Aufnahme von Mineralien, hauptsächlich Phosphat, und Wasser. Im Gegenzug versorgt die Pflanze ihn mit Photoassimilaten. Trotz der zentralen Bedeutung der Austauschmechanismen zwischen Pilz und Pflanze ist nur wenig darüber bekannt. Um die molekularen Grundlagen der Interaktion zwischen den Wurzeln der Leguminose Medicago truncatula und dem arbuskulären Mykorrhizapilz Rhizophagus irregularis besser zu verstehen, werden hier die Transportprozesse, die zwischen den Symbiosepartnern ablaufen, näher untersucht.
Die zellspezifische Regulation der Transkription potentieller M. truncatula Transporter Gene in arbuskelhaltigen und nicht-arbuskelhaltigen Zellen mykorrhizierter Wurzeln wird bestätigt. Ein Modell zur möglichen Verteilung von Kohlenhydraten in mykorrhizierten Wurzeln, nach dem Zucker in nicht-arbuskelhaltigen Zellen mobilisiert und symplastisch an arbuskelhaltige Zellen abgegeben werden, wird vorgestellt. Die Analyse eines Mykorrhiza-induzierten Hexose/H+ Symporter Gens, MtHxt1, liefert neue Einsichten in die Mechanismen der Kohlenhydratverteilung in mykorrhizierten Pflanzen. Metabolitanalysen von Wurzeln und Blättern einer knock-out Mutante dieses Gens zeigen dessen Einfluss auf den Kohlenhydrathaushalt der ganzen Pflanze und auf die Interaktion mit dem Pilz. Die Metabolitzusammensetzung von M. truncatula wird durch die Mykorrhiza Symbiose signifikant beeinflusst.
Darüber hinaus werden durch Transkriptomanalysen die molekularen Grundlagen der AM Symbiose auf der Seite des Pilzes analysiert. Arbuskeln wurden mittels Laser Capture Mikrodissektion direkt aus mykorrhizierten Wurzeln isoliert. Über 3200 pilzliche Transkripte weisen in diesen Arbuskeln im Vergleich zu extraradikalen Geweben ein deutlich verändertes Expressionslevel auf. Unter diesen Transkripten sind auch sechs zuvor unbekannte Gene, die für potentielle Transporter codieren und mit großer Wahrscheinlichkeit eine Rolle im Nährstoffaustausch zwischen Pilz und Pflanze spielen. Während die Substrate von drei potentiellen MFS Transportern noch unbekannt sind, spielen zwei potentiellen Zuckertransporter möglicherweise eine Rolle im Transport von Kohlenhydraten in Richtung des Pilzes.
Zusammengefasst bietet diese Arbeit neue Einsichten in Transportprozesse zwischen Pilz und Pflanze im Laufe der AM Symbiose. M. truncatula Transkript- und Metabolitlevel werden analysiert und die Transkriptomanalyse von R. irregularis liefert einen umfassenden Datensatz mit einer großen Menge an Informationen zu der noch unzureichend erforschten pilzlichen Seite der Symbiose für folgende Arbeiten.
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Predikce časného rozvoje funkce a rejekce transplanované ledviny / Prediction of graft function development and rejection of transplanted kidneyWohlfahrtová, Mariana January 2015 (has links)
Improving the short-term results of kidney transplantation did not result in improving the long-term function and survival of kidney allograft. Organ shortage and increasing number of marginal donors remains the key problem in transplant today. The quality of donor organ is critical for graft function development and survival. The aim is to improve understanding to ischemia/reperfusion injury and its consequences, predict delayed graft function and rejection, improve organ allocation strategy and identify patients suitable for safe drug minimization or complete withdrawal of immunosuppressive therapy. Analysis of donor kidneys identified poor tubular cell quality and low survival factor, Netrin-1 expression levels, to be associated with delayed graft function. We confirmed that reperfusion phase of ischemia/reperfusion injury leads to minimal morphological but significant molecular abnormalities. Dissociation observed in histology and molecular pathology finding calls for an integrated approach in donor quality organ evaluation and allocation for transplantation. Significant heterogeneity within donors with expanded criteria was shown and subgroup of organs at low risk of delayed graft function was identified. We suggested donor biopsies to be performed as a routine praxis in all kidneys...
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Analysis of the opsin repertoire in the Tardigrade Hypsibius dujardini provides insights into the evolution of opsin genes in PanarthropodaHering, Lars, Mayer, Georg January 2014 (has links)
Screening of a deeply sequenced transcriptome using Illumina sequencing as well as the genome of the tardigrade Hypsibius dujardini revealed a set of five opsin genes. To clarify the phylogenetic position of these genes and to elucidate the evolutionary history of opsins in Panarthropoda (Onychophora + Tardigrada + Arthropoda), we reconstructed the phylogeny of broadly sampled metazoan opsin genes using maximum likelihood and Bayesian inference methods in conjunction with carefully selected substitution models. According to our findings, the opsin repertoire of H. dujardini comprises representatives of all three major bilaterian opsin clades, including one r-opsin, three c-opsins, and a Group 4 opsin (neuropsin/opsin-5). The identification of the tardigrade ortholog of neuropsin/opsin-5 is the first record of this opsin type in a protostome, but our screening of available metazoan genomes revealed that it is also present in other protostomes. Our opsin phylogeny further suggests that two r-opsins, including an "arthropsin", were present in the last common ancestor of Panarthropoda. While both r-opsin lineages were retained in Onychophora and Arthropoda, the "arthropsin" was lost in Tardigrada. The single (most likely visual) r-opsin found in H. dujardini supports the hypothesis of monochromatic vision in the panarthropod ancestor, whereas two duplications of the ancestral panarthropod c-opsin have led to three c-opsins in tardigrades. Although the early-branching nodes are unstable within the metazoans, our findings suggest that the last common ancestor of Bilateria possessed six opsins: two r-opsins, one c-opsin, and three Group 4 opsins, one of which (Go opsin) was lost in the ecdysozoan lineage.
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Vlastnosti slinných proteinů flebotomů rodu Sergentomyia a Phlebotomus / Comparison and characterization of salivary proteins from Sergentomyia and Phlebotomus sand fliesPolanská, Nikola January 2020 (has links)
Sand flies (Diptera, Phlebotominae) are small biting insects and vectors of Leishmania spp. which cause medically and veterinary important disease - leishmaniasis. During the piercing of the host skin, sand fly females inject saliva to facilitate the blood feeding. The sand fly saliva is composed of many bioactive molecules which were shown to possess anti-inflammatory and anti-haemostatic functions. The saliva affects host's immunity in the bite site and consequently enhances the survival and development of transmitted pathogens. Most of the studies focus on salivary proteins and enzymes of sand flies belonging to Phlebotomus and Lutzomyia genera, while salivary proteins from sand flies of the third genus Sergentomyia were neglected so far. In this thesis we focused on comparison of salivary proteins from two Phlebotomus species, namely Phlebotomus perniciosus and Phlebotomus orientalis, and Sergentomyia schwetzi. These sand fly species differ not only by the ecology and geographical distribution but also by host preferences. Both Phlebotomus species prefer large or medium-size mammals as the bloodmeal source, particularly rabbits, hares and dogs for P. perniciosus and cattle, goats, sheep and humans for P. orientalis. Contrarily, Sergentomyia sand flies are known for preferred feeding on reptiles...
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Identifikace klíčových regulátorů genové exprese v savčím oocytu a embryu / Identification of key regulators of gene expression in mammalian oocyte and embryoJansová, Denisa January 2017 (has links)
Mammalian oocyte is a highly differentiated cell which gives rise to an embryo after fertilization. Importantly, fully-grown oocytes become transcriptionally inactive at the end of the growth phase. During following stages of development, i. e. meiotic maturation of the oocyte and early embryonic development, only transcripts previously synthesized and stored are used. The tight correlation between mRNA distribution and subsequent protein localization and function provides a mechanism of spatial and temporal regulation of gene expression used by various cell types. However, not much is known about mRNA localization and translation in the mammalian oocyte and early embryo. The aim of my thesis was to determine the localization of transcripts and components of translational machinery in the mammalian oocyte and embryo and to uncover the mechanisms of spatiotemporal regulation of translation as a prerequisite for correct oocyte and embryo development. We have shown that nuclei of both mouse and human oocytes contain RNA molecules and RNA binding proteins. Following the nuclear envelope breakdown (NEBD), translational hot-spots occur in the area surrounding the nuclear region. We suppose that mRNAs previously retained in the nucleus are released to the cytoplasm during NEBD and their subsequent...
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Predikce časného rozvoje funkce a rejekce transplanované ledviny / Prediction of graft function development and rejection of transplanted kidneyWohlfahrtová, Mariana January 2015 (has links)
Improving the short-term results of kidney transplantation did not result in improving the long-term function and survival of kidney allograft. Organ shortage and increasing number of marginal donors remains the key problem in transplant today. The quality of donor organ is critical for graft function development and survival. The aim is to improve understanding to ischemia/reperfusion injury and its consequences, predict delayed graft function and rejection, improve organ allocation strategy and identify patients suitable for safe drug minimization or complete withdrawal of immunosuppressive therapy. Analysis of donor kidneys identified poor tubular cell quality and low survival factor, Netrin-1 expression levels, to be associated with delayed graft function. We confirmed that reperfusion phase of ischemia/reperfusion injury leads to minimal morphological but significant molecular abnormalities. Dissociation observed in histology and molecular pathology finding calls for an integrated approach in donor quality organ evaluation and allocation for transplantation. Significant heterogeneity within donors with expanded criteria was shown and subgroup of organs at low risk of delayed graft function was identified. We suggested donor biopsies to be performed as a routine praxis in all kidneys...
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Gene expression profiling of two fish helminths throughout their complex life cycles. Are parasite’s life stages genetically decoupled?Gramolini, Laura 15 July 2024 (has links)
Komplexe Lebenszyklen sind eine häufige, aber anspruchsvolle Lebensweise von Parasiten. Parasiten mit komplexen Lebenszyklen infizieren nacheinander mehrere Wirte und passen sich an verschiedene ökologische Nischen an. Werden in diesem Szenario dieselben Gene in allen Wirten einheitlich exprimiert? Die Hypothese der adaptiven Entkopplung besagt, dass verschiedene Stadien in einem komplexen Lebenszyklus genetisch und evolutionär unabhängig sind, was bedeutet, dass die Selektion auf Parasitenmerkmale in einem Wirt keine Auswirkungen auf Merkmale in anderen Wirten hat.
Wir haben diese Hypothese anhand von zwei Parasitenarten getestet: dem Bandwurm Schistocephalus solidus und dem Fadenwurm Camallanus lacustris. Die Transkriptomsequenzierung wurde an Proben während ihrer komplexen Lebenszyklen durchgeführt. Die Genexpressionsanalyse wurde durchgeführt, um Gene zu identifizieren, die zwischen den Wirten, zwischen den Funktionsstadien und zwischen den Bedingungen unterschiedlich exprimiert werden. Darüber hinaus wurde mit einer Analyse der Anreicherung von Gensätzen untersucht, ob ähnliche biologische Funktionen von ähnlichen Genen in verschiedenen Stadien kodiert werden.
Unsere Ergebnisse zeigen signifikante Unterschiede in der Genexpression zwischen den verschiedenen Stadien, wobei keine positive Korrelation zwischen Stadien mit derselben Aufgabe oder demselben Wirt beobachtet wurde. Gene, die in einem Stadium hochreguliert (oder herunterreguliert) werden, werden in anderen Stadien nicht in ähnlicher Weise exprimiert. Dies spricht für die Unabhängigkeit der einzelnen Stadien bei der Genexpression, die es den Parasiten ermöglicht, ihren Phänotyp als Reaktion auf unterschiedlichen Selektionsdruck zu modulieren. Diese Ergebnisse bestätigen die Hypothese der adaptiven Entkopplung bei parasitären Würmern und bieten Einblicke in den evolutionären Erfolg dieser Lebensweise. / Complex life cycles are a common but demanding lifestyle among parasites. Parasites with complex life cycles sequentially infect multiple hosts, adapting to various ecological niches using information encoded within a single genome. In this scenario, are the same genes expressed consistently across all hosts, as might occur when parasite stages perform similar functions? The adaptive decoupling hypothesis posits that different stages in a complex life cycle are genetically and evolutionarily independent, meaning selection on parasite traits in one host does not affect traits in other hosts.
We tested this hypothesis using two species of parasites: the tapeworm Schistocephalus solidus and the nematode Camallanus lacustris, both of which have three-host life cycles. Transcriptome sequencing was performed on samples throughout their complex life cycles, generating transcriptomes from 10 stages of S. solidus and 7 stages of C. lacustris. Gene expression analysis was conducted to identify genes differentially expressed between hosts, between functional stages, and between conditions. Additionally, gene set enrichment analysis assessed whether similar biological functions are encoded by similar genes across stages.
Our findings demonstrate significant differences in gene expression across stages, with no positive correlation observed between stages sharing the same task or host. The highest correlation occurred between stages sampled close in time.
In conclusion, the lack of positive correlation between different life cycle stages indicates that genes up-regulated (or down-regulated) in one stage are not similarly expressed in other stages. This evidence supports the independence of each stage in gene expression, enabling parasites to modulate their phenotype in response to different selective pressures. These findings corroborate the adaptive decoupling hypothesis in parasitic worms with complex life cycles, offering insights into the evolutionary success of this lifestyle.
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