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Interactions of Mitochondria with Other Cellular Structures
Vinopalová, Martina ; Doležal, Pavel (advisor) ; Voleman, Luboš (referee)
In cells, mitochondria fulfil diverse set of roles, including a production of energy-rich molecules, which are necessary for proper functioning of the cell, calcium homeostasis, apoptosis and even biosynthesis of Fe-S centres, heme and steroids. To coordinate some of these processes with events occurring in the rest of the cell, mitochondria need to communicate with the other cellular structures through their physical contacts. Resulting intracellular platforms give rise to additional mitochondrial functions. This thesis summarizes current findings from the cells of mammalian model organisms and the budding yeast Saccharomyces cerevisiae about the interactions of this semiautonomous organelle with other cellular components and about the functions, which these interactions mediate.
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Peroxisomes and their role in energetic metabolism of the heart
Čejková, Denisa ; Kolář, David (advisor) ; Horníková, Daniela (referee)
Peroxisomes are small eucaryotic organelles, mainly known for their ability to create and break down hydrogen peroxide. However their enzymes play other significant roles, they participate in beta-oxidation of fatty acids with very long or branched chains, through alpha-oxidation they enable to process molecules that cannot go through beta- oxidation cycle, they also participate in early steps of synthesis of ether-lipid or bile acides. Above mentioned aspects make peroxisomes potentionally interesting for their possible influence on heart muscle metabolism, that is dependent on oxidative degradation of fatty acids, although not very much is known about this issue. The thesis focuses on biogenesis and function of peroxisomes, but also on their possible role in heart muscle metabolism.
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Interactions of Mitochondria with Other Cellular Structures
Vinopalová, Martina ; Doležal, Pavel (advisor) ; Voleman, Luboš (referee)
In cells, mitochondria fulfil diverse set of roles, including a production of energy-rich molecules, which are necessary for proper functioning of the cell, calcium homeostasis, apoptosis and even biosynthesis of Fe-S centres, heme and steroids. To coordinate some of these processes with events occurring in the rest of the cell, mitochondria need to communicate with the other cellular structures through their physical contacts. Resulting intracellular platforms give rise to additional mitochondrial functions. This thesis summarizes current findings from the cells of mammalian model organisms and the budding yeast Saccharomyces cerevisiae about the interactions of this semiautonomous organelle with other cellular components and about the functions, which these interactions mediate.
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Protein import into mitochondria and peroxisomes of parasitic protists
Žárský, Vojtěch ; Tachezy, Jan (advisor) ; Hampl, Vladimír (referee)
The presented thesis includes three related projects, that are linked by a common interest in the evolution of eukaryotic organelles and machineries that import proteins into these compartments. The first project considers the possibility of peroxisomes (eukaryotic organelles known in aerobic organisms) being conserved in two related anaerobic protists: a free-living amoeba Mastigamoeba balamuthi and a parasite Entamoeba histolytica. The most important hint for the presence of peroxisomes was the discovery of proteins that are homologous to known components of the peroxisomal protein import machinery. The second project aims to characterize the unknown protein translocase of the inner membrane (TIM) in the mitosomes (extremely reduced mitochondria) of an anaerobic protozoan Giardia intestinalis. We have discovered an important subunit of the mitosomal translocase (Tim44), which usually tethers the Hsp70/PAM (presequence translocase-associated motor) complex to the TIM translocon. The last project shows that the protein translocase of the outer mitochondrial membrane in trypanosomatids is related to a typical eukaryotic channel Tom40. This finding is important because the absence of Tom40 was previously considered an ancestral feature of trypanosomatids.
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