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Comparison of two Slovak Roma / Gypsy settlements in eastern Slovakia from an ethnographic perspective
Malík, Robert ; Jakoubková Budilová, Lenka (advisor) ; Jakoubek, Marek (referee)
This ethnographic study compares the sociocultural and economic status differences between two geographically and historically close Roma settlements in the Eastern Slovak region of Spiš. Using Pierre Bourdieu's concept of symbolic power, this study identifies factors that contribute to variations in integration and access to sociocultural and economic resources. Oscar Lewis' theory of the culture of poverty provides a complementary perspective on the past and present of both settlements.Participant observation, unstructured semi-structured interviews, and archive work with civil registers were the primary data collection methods used. The findings suggest that the more integrated settlement has greater access to symbolic resources, resulting in higher sociocultural and economic status. Conversely, the less integrated settlement is perceived as having insufficient access to these resources, leading to lower sociocultural and economic status. The study highlights the importance of integration and access to symbolic resources in shaping social, cultural, and economic power, offering a deeper understanding of the intricate power dynamics and inequalities between the majority and Roma communities.
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Epigenetic Dysregulation through Histone Modifications in Lymphoma
Hostaš, Ondřej ; Havránek, Ondřej (advisor) ; Malík, Radek (referee)
Lymphomas are a diverse group of malignant tumors that arise from lymphocytes, commonly affecting lymph nodes or the spleen. They are one of the most common types of tumors worldwide. Unfortunately, many subtypes have a poor prognosis, or are not currently fully curable with standard therapeutic approaches. Mutations in enzymes responsible for posttranslational modifications of histones are very common in certain subtypes of lymphoma, as well as in many other cancer types. These enzymes directly affect gene expression by changing the condensation state, and thus the accessibility, of chromatin. Some of these enzymes have been found to play an important role in the formation of germinal centers in lymphoid follicles. Therefore, their mutations can lead to uncontrolled proliferation and cancer development. Since many conventional therapeutic strategies are incapable of curing a large portion of lymphomas, novel and more targeted approaches are needed. Inhibition and/or modulation of the function of the aforementioned enzymes may be a basis for such approaches. Key words: lymphomas, epigenetic regulation, histone modifications, KMT2D, EZH2, CREBBP, EP300
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MicroRNAs encoded by polyomaviruses.
Zachovalová, Veronika ; Bruštíková, Kateřina (advisor) ; Malík, Radek (referee)
MicroRNAs are small regulating molecules of RNA that are encoded by orgamism's genome. Biogenesis of microRNA takes place partly in the nucleus and partly in the cytoplasm. Result of this biogenesis is a 22 nt long microRNA molecule. They are able to silence the genes thanks to sequence- specific degradation of a target mRNA or thanks to the repression of translation of target, complementary mRNA. In mammalian cells the mechanism of translational repression is more common. During this mechanism the microRNA molecule is not entirely complementary to 3'UTR of its target mRNA. Polyomaviruses are small, non-enveloped dsDNA viruses with a circular genome and icosahedral capsid composed of VP1 protein pentamers. These viruses belong in a group called onkoviruses, which can transform infected cells and contribute to development of serious illnesses such as Merkell cell carcinoma. Their genome encodes regulating proteins called T antigens, structural capsid proteins and also microRNAs. My main focus in this thesis will be SV40, MPyV, MCPyV, BKPyV and JCPyV encoded microRNA molecules. Key words: polyomaviruses, small interfering RNA, microRNA, siRNA, RNA interference, mouse polyomavirus, BK virus, JC virus, SV40
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Influence of transcription regulatory elemets on pre-mRNA splicing
Volek, Martin ; Staněk, David (advisor) ; Malík, Radek (referee)
In the process of pre-mRNA splicing introns are removed from pre-mRNA and exons are joined together. Current studies show, that about 95 % of genes, which contain more than two exons, can undergo alternative splicing. In this process some exons are included in or excluded from the final mRNA. Majority of pre-mRNA splicing take place co- transcriptionaly at this time RNA polymerase II is still attached to pre-mRNA. Alternative splicing is complex process that takes place in a close proximity of DNA and histones that might modulate alternative splicing decisions. Futher studies have validated fibronectin gene (FN1) and his alternative exons EDA and EDB (extra domain A and B) as suitably model for studying alternative splicing. Study using FN1 minigene reporter system, which is composed from EDA exon and two surrounding introns and exons, has proved that insertion of transcription enhancer SV40 infront of promotor, the level of EDA inclusion is decreased. So far, has not been prooved if this mechanism can function in real genome context and if distal transcription elements can influence alternative splicing. In this study, we have predicted transcription enhancer for FN1 gene by using The Ensemble Regulatory Build and FANTOM 5. The predicted transcription enhancer, is located 23,5 kbp upstream of TSS...
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Analysis of pre-mRNA alternative splicing products and their importance in breast cancer oncogenesis.
Hojný, Jan ; Kleiblová, Petra (advisor) ; Malík, Radek (referee) ; Boušková, Veronika (referee)
Breast cancer is the most common tumor disease diagnosed in women worldwide. The hereditary character of this disease is observed in 5-10 % of all cases, and it is usually caused by a pathogenic mutation in one of the predisposition genes. Although a variety of pathogenic mutations in the coding sequences of these genes was described, the cause of the disease is still unknown in many familial cases (> 50%). A great number of identified pathogenic mutations were localized in the consensus splicing sites, which results in the formation of aberrant mRNA splicing variants and their damaged protein isoforms. However, little is known about mutations affecting regulatory splicing sites, which can result in the translation of similarly affected mRNAs. In this work, we proposed a method for indirect detection of mutations affecting the natural splicing pattern of any gene of our interest based on multiplex PCR and NGS with high sensitivity. Verification of this method on the BRCA1 model gene revealed the presence of the total of 94 splicing variants in peripheral leucocytes and healthy breast and adjacent fat tissues. This is the most detailed catalogue of physically occurring BRCA1 mRNA variants thus far. The most commonly occurring variants, maintaining open reading frame, were quantified by RT-qPCR which...
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Influence of transcription regulatory elemets on pre-mRNA splicing
Volek, Martin ; Staněk, David (advisor) ; Malík, Radek (referee)
In the process of pre-mRNA splicing introns are removed from pre-mRNA and exons are joined together. Current studies show, that about 95 % of genes, which contain more than two exons, can undergo alternative splicing. In this process some exons are included in or excluded from the final mRNA. Majority of pre-mRNA splicing take place co- transcriptionaly at this time RNA polymerase II is still attached to pre-mRNA. Alternative splicing is complex process that takes place in a close proximity of DNA and histones that might modulate alternative splicing decisions. Futher studies have validated fibronectin gene (FN1) and his alternative exons EDA and EDB (extra domain A and B) as suitably model for studying alternative splicing. Study using FN1 minigene reporter system, which is composed from EDA exon and two surrounding introns and exons, has proved that insertion of transcription enhancer SV40 infront of promotor, the level of EDA inclusion is decreased. So far, has not been prooved if this mechanism can function in real genome context and if distal transcription elements can influence alternative splicing. In this study, we have predicted transcription enhancer for FN1 gene by using The Ensemble Regulatory Build and FANTOM 5. The predicted transcription enhancer, is located 23,5 kbp upstream of TSS...
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Use of antibodies for the characterization of chromatin modifications in Saccharomyces cerevisiae
Kovaľová, Libuša ; Hodek, Petr (advisor) ; Malík, Radek (referee)
Transcription of precursor mRNA (pre-mRNA) and its splicing were originally conceived as two separate processes. Using Saccharomyces cerevisiae as a model, it was shown that the assembly of the complex catalyzing pre-mRNA splicing (spliceosome) can occur cotranscriptionally, i. e., during the time before the termination of transcription by RNA polymerase II. Research on cotranscriptional splicing revealed that proteins involved in transcription and specific chromatin modifications may affect pre-mRNA splicing and its regulation. It is also possible that spliceosome assembly and chromatin modifications can affect each other. Prp45, the yeast ortholog of the human transcription coregulator SKIP/SNW1, has been previously associated only with splicing. The results obtained in our laboratory suggest that Prp45 could be used as a regulator coupling the processes of transcription and splicing. We have shown that PRP45 has genetic interactions with factors important for transcription elongation, as well as chromatin modifications, and that it affects early stage of spliceosome assembly. The aim of this bachelor project was document the relationship between the physiological role of Prp45 and H3K4 trimethylation using chromatin immunoprecipitation. It was found that prp45(1-169) mutation does not markedly...
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