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Polyglutamylation as a Posttranslational Tubulin Modification
Bašta, Miroslav ; Bařinka, Cyril (advisor) ; Dráber, Pavel (referee)
α-tubulin is an essential protein for every eukaryotic cell. Together with β-tubulin, it polymerises into microtubules and participates thus in creating and maintaining cellular structures and presents a cell-wide interaction platform for a plethora of microtubule associating proteins. Primary sequences of the disordered C-termini of both α- and β-tubulin are the least conserved among tubulin isotypes and their variability is further increased by the presence of various post-translational modifications. The genetically coded, tyrosinated C-terminus of α-tubulin can be either shortened by one, two or three amino acids resulting in detyrosinated, Δ2, or Δ3 variants, respectively or it can be extended by the addition of polyglutamate or polyglycine chains. The tubulin tyrosine ligase-like (TTLL) protein family consists of 14 enzymes that participate in tubulin glutamylation, glycylation, and tyrosination. The glutamylases have two distinct activities, initiation and elongation of the polyglutamate chain. Initiases link the first glutamate residue to the γ-carboxyl group of one of the glutamates of tubulin C-termini to create a fork in the amino acid sequence. Elongases then recognise the branching glutamate and build up the polyglutamate sidechain one residue at the time. TTLL11 is an elongase of...
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Uloha kataninu, ATPázy štěpící mikrotubuly, při modulaci buněčné motility a proliferace glioblastomových buněk.
Uhlířová, Jana ; Dráber, Pavel (advisor) ; Libusová, Lenka (referee)
Glioblastomas are the most common and the deadliest types of brain tumours. Due to their highly invasive behaviour, they are incurable by convencial therapeutical strategies. It was shown that some components of microtubules, namely class III β-tubulin, γ-tubulin and microtubule severing protein spastin are overexpressed in glioblastoma cell lines as well as glioblastomas. This diploma thesis is focused on the expression, subcellular distribution and function of katanin, another microtubule-severing enzyme, in gliobastoma cell lines. Katanin is formed by catalytic (p60) and regulatory (p80) subunits. Expression and cellular localization of both katanin subunits was studied in panel of human glioblastoma cell lines isolated form adults (T98G, U87MG, U118MG and U138 MG) and child (KNS42). Data presented in this thesis demonstrated that katanin subunits were overexpresed both on transcript and protein levels in T98G, U87MG and KNS42 cell lines, but not in U138MG and U118MG cell lines when compared to normal non- transformed human astrocytes. Immunofluorescence microscopy revealed that both katanin subunits were diffusively distributed in cytoplasm and concentrated on spindle poles of mitotic cells and on leading edges of migrating cells. Examination of cell motility revealed that velocities in...
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Functional characterization of selected microtubule regulatory
Vinopal, Stanislav ; Dráber, Pavel (advisor) ; Binarová, Pavla (referee) ; Hašek, Jiří (referee)
Microtubules (MTs) play crucial roles in intracellular organization and transport, cell polarity, motility, signalling, division and differentiation. MTs form complex arrays, which are, due to their highly dynamic nature, capable of rapid reorganization in response to cellular requirements. Dynamics, stability and spatial organization of MTs are regulated by many factors including MT regulatory proteins. In the presented study we functionally characterized three selected MT regulatory proteins: Ca2+ -sensor STIM1, MT severing protein spastin and γ-tubulin that is essential for MT nucleation. We found out that activation of bone marrow mast cells (BMMCs) leads to the formation of plasma membrane protrusions containing MTs. Formation of these MT protrusions is dependent on an influx of extracellular Ca2+ regulated by protein STIM1, located in endoplasmic reticulum. STIM1 associates with MTs and its depletion prevents formation of MT protrusions. This indicates that Ca2+ ions might be involved in MT regulation. Since STIM1 depletion also causes defects in chemotaxis, we propose that MT protrusions might be involved in sensing of external signals recognized by BMMCs. Glioblastoma multiforme is the most common and most aggressive malignant primary brain tumor in humans. We demonstrated that MT severing...
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Following the Arp2/3-based processes in plant cells
Fišerová, Jindřiška ; Opatrný, Zdeněk (advisor) ; Binarová, Pavla (referee) ; Dráber, Pavel (referee)
1. ABSTRACT An actin cytoskeleton comprises an essential cytoskeletal structure that organizes a cytoplasm during number of processes occurring in animal and plant cells, such as cell division and growth, formation of membrane protrusions and cellular movement or cytoplasmic streaming. A dynamic actin net and an exact spatial and temporal actin filament organization is, therefore, necessary for correct growth processes and development of multicellular organism. Depolymerization and re-establishment of actin arrays is mediated by actin associated proteins. Among them, an Arp2/3 complex (actin related protein 2 and 3) plays an important role as a catalyst of the actin filament nucleation and, thus, enables the formation of dynamic actin network. In non-plant cells, Arp2/3 complex-dependent polymerization of actin filaments is required for movement of whole cells (fibroblasts or keratocytes), it drives organels and pathogens throughout the cell or mediates endocytic processes. The role of the Arp2/3 complex in non-motile plant cells is despite the considerable effort over last three years far from being understood. Unlike animals, where loss-of-function mutations in the Arp2/3 complex are lethal, only limited number of cell types show significant phenotype in Arabidopsis mutants. The evidence exists that the...
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Regulatory mechanisms of centrosomal microtubule nucleation
Klebanovych, Anastasiya ; Dráber, Pavel (advisor) ; Hašek, Jiří (referee) ; Vomastek, Tomáš (referee)
The spatio-temporal organization and dynamic behavior of microtubules accurately react to cellular needs during intracellular transport, signal transduction, growth, division, and differentiation. The cell generates centrosomal microtubules de novo with the help of γ-tubulin complexes (γTuRCs). The post-translational modifications fine-tune microtubule nucleation by targeting the proteins, interacting with γTuRCs. However, the exact signaling pathways, regulating centrosomal microtubule nucleation, remain mostly unknown. In the presented thesis, we functionally characterized protein tyrosine phosphatase SHP-1 and E3 UFM-protein ligase 1 (UFL1) with its interacting protein CDK5RAP3 (C53) in the regulation of centrosomal microtubule nucleation. We also elucidated the role of actin regulatory protein profilin 1 in this process. We found that SHP-1 formed complexes with γTuRC proteins and negatively regulated microtubule nucleation by modulating the amount of γ-tubulin/γTuRC at the centrosomes in bone marrow-derived mast cells (BMMCs). We suggested a novel mechanism with centrosomal tyrosine-phosphorylated Syk kinase, targeted by SHP-1 during Ag-induced BMMCs activation, regulating microtubules. We showed for the first time that UFL1/C53 protein complex is involved in the regulation of microtubule...
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The role of evolutionarily conserved proteins BIR-1/Survivin and SKP-1 in the regulation of gene expression
Kostrouch, David ; Kostrouch, Zdeněk (advisor) ; Dráber, Pavel (referee) ; Pacák, Karel (referee)
SKIP and BIR/Survivin are evolutionarily conserved proteins. SKIP is a known transcription and splicing cofactor while BIR-1/Survivin regulates cell division, gene expression and development. Loss of function of C. elegans SKIP (SKP-1) and BIR-1 induces overlapping developmental phenotypes. In order to uncover the possible interactions of SKP-1 and BIR-1 on the protein level, we screened the complete C. elegans mRNA library using the yeast two-hybrid system. These experiments identified partially overlapping categories of proteins as SKP-1 and BIR-1 interactors. The interacting proteins included ribosomal proteins, transcription factors, translation factors and cytoskeletal and motor proteins suggesting involvement of the two studied proteins in multiple protein complexes. To visualize the effect of BIR-1 on the proteome of C. elegans we induced a short time pulse BIR-1 overexpression in synchronized L1 larvae. This led to a dramatic alteration of the whole proteome pattern indicating that BIR-1 alone has the capacity to alter the chromatographic profile of many target proteins including proteins found to be interactors in yeast two hybrid screens. The results were validated for ribosomal proteins RPS-3, RPL-5, non-muscle myosin and TAC-1, a transcription cofactor and a centrosome associated...
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Following the Arp2/3-based processes in plant cells
Fišerová, Jindřiška ; Opatrný, Zdeněk (advisor) ; Binarová, Pavla (referee) ; Dráber, Pavel (referee)
1. ABSTRACT An actin cytoskeleton comprises an essential cytoskeletal structure that organizes a cytoplasm during number of processes occurring in animal and plant cells, such as cell division and growth, formation of membrane protrusions and cellular movement or cytoplasmic streaming. A dynamic actin net and an exact spatial and temporal actin filament organization is, therefore, necessary for correct growth processes and development of multicellular organism. Depolymerization and re-establishment of actin arrays is mediated by actin associated proteins. Among them, an Arp2/3 complex (actin related protein 2 and 3) plays an important role as a catalyst of the actin filament nucleation and, thus, enables the formation of dynamic actin network. In non-plant cells, Arp2/3 complex-dependent polymerization of actin filaments is required for movement of whole cells (fibroblasts or keratocytes), it drives organels and pathogens throughout the cell or mediates endocytic processes. The role of the Arp2/3 complex in non-motile plant cells is despite the considerable effort over last three years far from being understood. Unlike animals, where loss-of-function mutations in the Arp2/3 complex are lethal, only limited number of cell types show significant phenotype in Arabidopsis mutants. The evidence exists that the...
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Molecular characterization of γ -tubulin interactions with signalling molecules
Macůrek, Libor ; Dráber, Pavel (advisor) ; Binarová, Pavla (referee) ; Svoboda, Augustin (referee)
52 V. CONCLUSIONS The results of presented PhD thesis can be summarized as follows: For the first time it has been demonstrated that γ-tubulin forms complexes with αβ-tubulin dimers in brain tissue as well as in other models of neuronal differentiation. Two forms of γ- tubulin have been identified in complexes of various sizes. It has been shown that γ-tubulin is posttranslationally modified. One of the identified posttranslational modifications of γ-tubulin is phosphorylation that appears to depend on Src family kinase activity. It has been proposed that posttranslational modifications of γ-tubulin may regulate interactions of γ-tubulin with αβ-tubulin heterodimers or other associated proteins during neurogenesis. It has been shown that γ-tubulin associates with protein tyrosine kinases involved in signal transduction events. γ-Tubulin interaction with Src family kinases significantly increased after long-term RA-activation embryonal carcinoma P19 cells. A similar increase has been observed after rapid activation of mast cells, indicating that this regulatory mechanism is not restricted to a particular model system. In both models, Src family kinases bound to γ-tubulin are active and phosphorylate proteins present in γ-tubulin complexes. Fyn kinase interacts with γ-tubulin through its SH2 domain in a...
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