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DNA markery rezistencie voči biotickému stresu u uhorky siatej
Zvalová, Monika
Thanks to ever-advancing biotechnology techniques, DNA markers have become an integral part of the study of the plant genome. Knowledge of ideal molecular markers is widely applicable and helpful in genome mapping, genetic map construction, systematic taxonomy or conventional breeding. Compared to conventional approaches, DNA markers have many advantages, such as high stability, reliability and they are not affected by the environment. The diploma thesis deals with the application of various types of genetic markers in the study of regions of the cucumber genome responsible for resistance or susceptibility to selected biotic stressors, especially bacteries and viruses. It compares the effectiveness of RAPD with SCAR and CAPS markers. Furthermore, suitable and unsatisfactory genetic markers against angular leaf spot and disease caused by Zucchini yellow mosaic virus have been defined, which contribute to the economic losses of many crops every year. The work includes optimization of the PCR protocol and sequence analysis of selected amplified regions of the cucumber genome and their subsequent comparison in the NCBI database. For the future, a practical use of the results is proposed for cooperation with the MORAVOSEED CZ a.s company. The conclusion of the laboratory work can be helpful in the perspective use of markers specific to PSyLA and ZYMV.
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Study of genetic diversity of Pectinatella magnifica (Leidy, 1851) colonies
MORAVCOVÁ, Vendula
Pectinatella magnifica is a freshwater organism from the bryozoan group, living in oligotrophic and mesotrophic waters where the temperature reaches 20°C during the year. It was first found and described by Joseph Leidy in the Philadelphia area in 1851. Although the original place of occurrence is North America, it is currently known as an invasive organism on other continents as well. Representatives of the species Pectinatella magnifica live in colonies with a characteristic spherical shape, which makes it easy to recognize and identify. These spherical colonies are covered with a community of zooids that produce a gel-like substance filling the colony itself. The reproduction of bryozoans is both sexual and asexual, with the non-sexual part exceeding the sexual part. The product of asexual reproduction are internal buds, so-called statoblasts, equipped with hooks, thanks to which they can attach to any substrate, which enables easy distribution even over long distances through otherwise difficult terrain. Although this is an ancient group with a predominance of asexual, therefore clonal, reproduction, the sexual part of reproduction enables the emergence of mutations and adaptation to new conditions. The dissertation is focused on determining the genetic diversity of colonies taken from the territory southern Bohemia and the surrounding area using molecular marker techniques. Two molecular techniques were used for processing genetic analyses, namely AFLP (Amplified Fragment Length Polymorphism) and ISSR (Inter Simple Sequence Repeat). Both techniques use universal primers to determine similarity between organisms.
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The use of novel technologies in the identification of unique molecular markers for minimal residual disease assessment in acute leukemia patients
Jančušková, Tereza ; Peková, Soňa (advisor) ; Jarošová, Marie (referee) ; Lysák, Daniel (referee)
Acute leukemias (AL) comprise a heterogeneous group of hematologic malignancies, and individual patient responses to treatment can be difficult to predict. Monitoring of minimal residual disease (MRD) is thus very important and holds great potential for improving treatment strategies. Common MRD targets include immunoglobulin heavy chain or T-cell receptor gene rearrangements, recurrent cytogenetic abnormalities and mutations in important hematological genes. Whereas in the majority of adult acute lymphoblastic leukemia patients a suitable MRD target can be identified, in adult acute myeloid leukemia patients well-characterized targets are found in only half of cases. The identification of new specific molecular markers of leukemic blasts for MRD assessment, particularly in AML patients, is therefore highly desirable. Our aim was to develop a flexible strategy for mapping of cytogenetically identified unique clone-specific abnormalities down to the single nucleotide level and, based on the sequence, design a specific real-time PCR assay for MRD assessment in AL patients without any previously described MRD marker. Using a combination of cytogenetic (chromosome banding, chromosome microdissection), molecular cytogenetic (mFISH, mBAND) and molecular biological (next- generation sequencing, long-range...
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The use of novel technologies in the identification of unique molecular markers for minimal residual disease assessment in acute leukemia patients
Jančušková, Tereza
Acute leukemias (AL) comprise a heterogeneous group of hematologic malignancies, and individual patient responses to treatment can be difficult to predict. Monitoring of minimal residual disease (MRD) is thus very important and holds great potential for improving treatment strategies. Common MRD targets include immunoglobulin heavy chain or T-cell receptor gene rearrangements, recurrent cytogenetic abnormalities and mutations in important hematological genes. Whereas in the majority of adult acute lymphoblastic leukemia patients a suitable MRD target can be identified, in adult acute myeloid leukemia patients well-characterized targets are found in only half of cases. The identification of new specific molecular markers of leukemic blasts for MRD assessment, particularly in AML patients, is therefore highly desirable. Our aim was to develop a flexible strategy for mapping of cytogenetically identified unique clone-specific abnormalities down to the single nucleotide level and, based on the sequence, design a specific real-time PCR assay for MRD assessment in AL patients without any previously described MRD marker. Using a combination of cytogenetic (chromosome banding, chromosome microdissection), molecular cytogenetic (mFISH, mBAND) and molecular biological (next- generation sequencing, long-range...
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The use of novel technologies in the identification of unique molecular markers for minimal residual disease assessment in acute leukemia patients
Jančušková, Tereza
Acute leukemias (AL) comprise a heterogeneous group of hematologic malignancies, and individual patient responses to treatment can be difficult to predict. Monitoring of minimal residual disease (MRD) is thus very important and holds great potential for improving treatment strategies. Common MRD targets include immunoglobulin heavy chain or T-cell receptor gene rearrangements, recurrent cytogenetic abnormalities and mutations in important hematological genes. Whereas in the majority of adult acute lymphoblastic leukemia patients a suitable MRD target can be identified, in adult acute myeloid leukemia patients well-characterized targets are found in only half of cases. The identification of new specific molecular markers of leukemic blasts for MRD assessment, particularly in AML patients, is therefore highly desirable. Our aim was to develop a flexible strategy for mapping of cytogenetically identified unique clone-specific abnormalities down to the single nucleotide level and, based on the sequence, design a specific real-time PCR assay for MRD assessment in AL patients without any previously described MRD marker. Using a combination of cytogenetic (chromosome banding, chromosome microdissection), molecular cytogenetic (mFISH, mBAND) and molecular biological (next- generation sequencing, long-range...
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The use of novel technologies in the identification of unique molecular markers for minimal residual disease assessment in acute leukemia patients
Jančušková, Tereza ; Peková, Soňa (advisor) ; Jarošová, Marie (referee) ; Lysák, Daniel (referee)
Acute leukemias (AL) comprise a heterogeneous group of hematologic malignancies, and individual patient responses to treatment can be difficult to predict. Monitoring of minimal residual disease (MRD) is thus very important and holds great potential for improving treatment strategies. Common MRD targets include immunoglobulin heavy chain or T-cell receptor gene rearrangements, recurrent cytogenetic abnormalities and mutations in important hematological genes. Whereas in the majority of adult acute lymphoblastic leukemia patients a suitable MRD target can be identified, in adult acute myeloid leukemia patients well-characterized targets are found in only half of cases. The identification of new specific molecular markers of leukemic blasts for MRD assessment, particularly in AML patients, is therefore highly desirable. Our aim was to develop a flexible strategy for mapping of cytogenetically identified unique clone-specific abnormalities down to the single nucleotide level and, based on the sequence, design a specific real-time PCR assay for MRD assessment in AL patients without any previously described MRD marker. Using a combination of cytogenetic (chromosome banding, chromosome microdissection), molecular cytogenetic (mFISH, mBAND) and molecular biological (next- generation sequencing, long-range...
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Comparison of ITS nrDNA and alternative markers for fungal metabarcoding in environmental samples
Zelenka, Tomáš ; Kolařík, Miroslav (advisor) ; Mašek, Tomáš (referee)
The study of fungal diversity may lead to many fundamental discoveries and conclusions. Molecular genetics, and particularly high throughput sequencing methods using short DNA fragments as barcodes, has recently experienced a boom. The most frequently used marker for fungal research is the partial region of nuclear ribosomal DNA called ITS (Internal Transcribed Spacer). It occurs in the form of tandem repetitions of up to 200 copies. This fact greatly simplifies its amplification from the environment but also introduces some negatives. One of them can be an existence of intragenomic and intraspecific variability which confounds diversity estimates by exaggerating the real number of species. Using alternative low-copy markers can easily prevent these problems. In this study EF-1α and RPB2 protein- coding genes were compared with traditionally used ITS1 and ITS2 markers. An artificial mock community was created by blending genomic DNA of different fungal lineages. The community was sequenced for all markers and the data were processed according to guidelines commonly used in environmental studies. The results show that ITS2 is unequivocally a more suitable marker for environmental studies than other compared markers. The average coefficient of overestimation was deemed to be approximately two for ITS1, ITS2,...
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Genetic variability of \kur{Isaria} genus in Czech Republic
ČÁPOVÁ, Aneta
My diploma thesis deals with genetic variability of entomopathogenic fungi of the Isaria genus encountered in the Czech Republic. Individual representative of the genus can be found in soil where they attack all developmental stages of insects, giving preference to larvae and pupae. The Isaria fungi find application first and foremost where plants have to be provided biological protection. In case of mitosporic fungi is the precise identification very difficult, taxonomy is often unclear in many genera, including the genus Paecilomyces/Isaria to demonstrate their polyphyletic nature. The fungi are classified primarily with reliance on morphological studies. The most common markers used to identify fungi are the shapes and sizes of their conidia and the biological properties (germination of spores, tests of biological efficiency). Identification made in consideration of the morphological markers is inaccurate and very variable. To overcome those accuracies, there are very useful molecular DNA markers, which can be relevant in ecology, biology and in fungi genetics. This paper relies on applying the ITS region (Internal Transcribed Spacer) as a molecular marker. ITS regions are partial constituent rDNA carrying no code - that is why the regions are likely to accumulate evolutionary changes in the DNA sequence, which makes them suitable for extensive use in taxonomic analyses of many organisms. The study results in a phylogenetic trees constructed by comparing different sequences of ITS regions obtained from the samples of entomopathogenic fungi of the Isaria genus gathered in the Czech Republic during the monitoring stage 2013 to 2014. Thereunder detection of Isaria sp. occurring in the Czech Republic.
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Molecular aspects of interspecific hybridization of sturgeons related to polyploidy and in situ conservation
HAVELKA, Miloš
Sturgeons (Chondrostei: Acipenseriformes) display markedly disjunct distributions with a wide occurrence in the northern hemisphere. Their unique benthic specializations, conserved morphology, evolutionary age, the variation in their basic diadromous life history, and the large public interest due to their near extinction or critically endangered status make sturgeons and paddlefishes one of the most interesting group of vertebrates. In addition to that, ploidy diversity of Acipenseriformes possessing three ploidy groups having ~ 120 chromosomes, ~ 240 ? 270 chromosomes and ~ 360 chromosomes provides unique model for investigation of evolutionary processes which were going through the genome duplication events. Sturgeons are also notoriously known for their strong propensity to interspecific and intergeneric hybridization which can result in hybrids with various ploidy levels. All these facts make sturgeon genetics and cytogenetics a thriving but also complicated area for research. In the present work, the role of genome duplication and functional reduction evens in evolution of sturgeon species as well as sturgeons? ploidy levels and ploidy relationships among Acipenseriformes were investigated using molecular markers. In addition to that, clarification of origin of abnormal ploidy levels and observation of segregation pattern of microsatellite alleles in the course of hybridization of polyploid sturgeon species were included into this study. With regard to the all considerations and observations provided by this study we concluded that evolution of sturgeon species is still widely dynamic and ongoing process which might goes through the allopolyplodization as well as autopolyplidization events.
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Application of DNA barcoding on genus \kur{Folsomia} (Collembola) and mitochondrial geonome of \kur{F. candida}
SLÁMOVÁ, Martina
Mitochondrial molecular marker COI was tested for use in species identification of selected species of genus Folsomia (Collembola). Marker was succesfuly amplified and sequenced. Dendrogram constructed by Neighbor-Joining method with Kimura-2-Parameter model grouped all individuals into presumed species clusters and high intraspecific variability of F. quadrioculata suggests the existence of cryptic species. Furthermore, 65 % of mitochondrial geonome of F. candida was obtained with 16 tRNA genes, 9 proteincoding genes and 2 rRNA genes identified. So far the genome characteristics correspond to the one described in G. hodgsoni.
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