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Spreading of praying mantis (Mantis religiosa) in Europe
Vitáček, Jakub ; Janšta, Petr (advisor) ; Gvoždík, Václav (referee)
Climate change is one of the most important factor determining species ranges. In Europe there is now evidence for northward areal expansion in many Mediterranean insects including the praying mantis (Mantis religiosa). This species is the only representative of the order Mantodea inhabiting central Europe. The northern edge of the species distribution currently reaches latitude 53ř North. Although, the praying mantis is well known insect there is not enough evidence about its phylogeography. In this work three mitochondrial genes (COI, COII, Cyt b) were selected for phylogenetic study. Results indicate three statistically supported distinct lineages in Europe: Eastern European, Central European and Western European. Presumably these lineages are consistent with isolation during the last glacial and re-colonization from glacial refugia. Reduced haplotype diversity on the northern edge suggests currently established populations at the northern distribution border. To validate mtDNA results it was also considered four microsatellite loci. Due to different type of inheritance mtDNA and nuclear DNA it is possible to compare two independent genetic datasets. Microsatellite analysis confirmed results obtained on mitochondrial data. Three major genetic clusters were found: east, west and central. Spatial...
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The testing of familiar relationship in the identification genetics
Bobková, Alena ; Vaněk, Daniel (advisor) ; Zemanová, Zuzana (referee)
This bachelor's thesis analyses kinship testing in identification genetics, which is a discipline enabling the genetic identification of individuals and the determination of genetic relatedness between them. This thesis covers a wide range of applications from forensic analysis through genealogical studies to biodiversity conservation. This field has been rapidly growing and gaining on importance since the 1980s, when the foundations of DNA fingerprinting were laid based on the discovery of hypervariable minisatellite regions in the genome. This thesis aims to provide an overview of methods and techniques that are used for genetic identification and kinship testing. The thesis discusses genetic markers such as STRs or SNPs, which are the basis for genetic profiling, are discussed. In addition statistical methods for evaluating genetic match and methodologies for determining the probability of kinship are also discussed. Finally, practical applications of identification genetics are presented, including its use in forensic science or in case of solving genealogical questions. The potential and future development of the technologies and their impact on society is discussed at the end of the thesis. Thus, the thesis contributes to a better understanding of the importance and opportunities of...
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New possibilities to distinguish monozygotic twins
Letková, Kristína ; Kulichová, Iva (advisor) ; Priehodová, Edita (referee)
The necessity of distinguishing monozygotic twins from a genetic point of view is important not only for determining paternity, when it is decided which of two identical twins is the father, but also, for example, for criminal cases, where it is necessary to identify the perpetrator who is one of the monozygotic twins. In addition to analyzing and evaluating molecular biological methods, the work also deals with monozygotic twins themselves, their emergence and the causes of their emergence. The topic affects both forensic genetics and medical fields.
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Global phylogeography of the deep-sea fishes
Knězů, Tereza ; Musilová, Zuzana (advisor) ; Vukićová, Jasna (referee)
Phylogeography of deep-sea fish remains poorly explored, largely due to the extreme conditions in which these organisms live and limited technological capabilities for researching these species. The aim of this thesis is to summarize the information known about the phylogeography of deep-sea fish, identify factors influencing population distributions, and connect them on a global scale. The distribution of deep-sea fish populations is influenced by physical, topographic, and hydrographic factors. Their connectivity is driven by the migratory abilities of fish and the utilization of marine currents for their dispersion. Migration is divided into vertical and horizontal. The vast majority of deep sea fish undergo some form of migration, at least during ontogenetic development. The most common is diurnal vertical migration, where fish regularly move to shallower depths at night for feeding. Molecular methods, mainly mitochondrial DNA markers, were used for research to determine the phylogenetic tree of species. The results suggest that the topography of the seafloor is rarely a barrier to the flow of genetic information. Furthermore, the results often refute the hypothesis of isolation caused by the distance between populations. They often exhibit a relatively high rate of panmixia. When speciation...
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The role of mitochondrial DNA in reproduction
Svobodová, Mariana ; Daňková, Pavlína (advisor) ; Jelínková, Ladislava (referee)
The bachelor's thesis focuses on the role of mitochondrial DNA (mtDNA) in human reproduction, especially describing the differences in mtDNA dynamics in oogenesis, spermatogenesis and early embryo development. The physiological function of mtDNA is complemented by its pathologies and their effect on fertility and the ability of the embryo to implant successfully. Furthermore, mtDNA is discussed as a possible diagnostic marker in the evaluation of the quality of sperm, eggs and embryos. These findings of these studies are especially significant for assisted reproduction, where the goal is to select the highest quality embryo with the greatest implantation potential. The work also briefly mentions the presence of cell free mtDNA in the mother's blood and its connection with the development of preeclampsia. Key words: mtDNA, mitochondria, reproduction, (in)fertility
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Optimization of real-time PCR method for quantification of human mtDNA in clinical samples
LOSKOT, Martin
This bachelor thesis dealing with measuring mitochondrial DNA (mtDNA) and how is it important to pathological conditions. Mitochondria are one of the cell organelles in eukaryotic cells. They are important to energy metabolism, aging process, and apoptosis. In current studies mitochondrial dysfunctions cause mitochondrial diseases and common illnesses, for example cardiovascular diseases, brain pathology or cancer. Studies show, that copy number of mtDNA correlates with state of health and aging process. Copy number of mtDNA is often measured by ratio of mtDNA to nuclear DNA. Measuring mtDNA of peripheral blood is appropriate indicators for mitochondrial functions because decreased copy number of mtDNA correlates with decreased function of mitochondria. We don't know, how copy number of mtDNA influence on illnesses, because it doesn't still clarify. However, studies show, that copy number of mtDNA can be biomarker of control of state of health, when we take real time measurement. In the practical part of this bachelor thesis describe preparation of samples from buccal swabs and from peripheral blood. It also describes method of measuring mtDNA by real-time PCR. There is calculation of copy number of mtDNA and evaluation of our results too. As part of the measurement optimization are described differences between two methods for diagnostic of relative copy number of mtDNA.
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Migrations in the African Sahel through the view of the genetic diversity of control segment of mitochondrial DNA
Adámková, Kristýna ; Černý, Viktor (advisor) ; Frynta, Daniel (referee)
Sub-Saharan Africa is the region with the highest diversity of anatomically modern humans (AMH). With the use of genetic analysis of mostly uniparental loci, gradually we can uncover the migratory activity of humans long time ago. This work focuses on the African Sahel. It is a long, horizontal strip bordered by the Sahara Desert and tropical rainforests across the entire continent. Favorable environmental conditions and the absence of a geographical barrier are suitable not only for mobile herders, but also for sedentary farmers. These provisos create high migration aktivity in the area. In this work, I newly sequenced 474 mitochondrial DNA samples of 11 populations. Populations of pastoralists and farmers are spread all over Sahel/Savannah belt. Intrapopulation analysis assessed diversity within the population and generally showed low values in pastoral populations, especially Fulani pastoralists in the western Sahel. Interpopulation analysis revealed bigger differences between individual populations than between populations clustered in the subsistence group of pastoralists or farmers, within regions or within language. The work included populations with Afro-Asiatic, Niger-Congo and Nilo-Saharan language families. Thanks to the Migrate-n program, in this work I was able to confirm the...
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Hereditary Mitochondrial Disorders Caused by Oxidative Phosphorylation Disfunction
Hanušová, Eva ; Ehler, Edvard (advisor) ; Pavlasová, Lenka (referee)
Hereditary Mitochondrial Disorders Caused by Oxidative Phosphorylation Dysfunction This bachelor thesis deals with problems of hereditary mitochondrial disorders that are caused by various dysfunctions of proteins in oxidative fosforylation known as OXPHOS complex. Following recherche provides the reader with information about the genom and the structure of mitochondria where the OXPHOS is realized and about its structure and progress. I describe basic facts about various mutations in nuclear and mitochondrial DNA that negatively affect function of OXPHOS complex and the biogenesis of mitochondria. The focus of this work is to summarize the newest data of individual diseases - their clinical manifestation, etiopatogenesis, prevalance in population and its possible treatment and prevention. Key words: hereditary, mtDNA, mitochondrial diseases, OXPHOS complex
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The genetic links around the Red Sea as revealed by the mtDNA
Čížková, Martina ; Černý, Viktor (advisor) ; Rídl, Jakub (referee)
The Red Sea region is one of the important places that allow us to uncover traces of the evolution of anatomically modern humans. Besides the questions related to its expansion out of Africa, this region is also important in terms of the mutual influence between populations of Africa and Arabia that after a long period of isolation and genetic differentiation related to climate change in the Pleistocene and subsequent development of seaways and land routes in the Holocene began to contact with each other more frequently. Number of genetic analyzes has been done but some issues concerning on the later development still remain inadequately answered, mainly because of insufficient material. This work is focused on the analysis of 200 mtDNA sequences of four Sudanese populations - two populations of nomadic herdsmen Rashaida and Beja living in the close neighborhood around the city of Kassala and speaking different languages and two populations of the Nile Valley with settled way of life. Analysis of the intrapopulation level revealed much higher diversity of the sedentary populations (in this work the sedentary populations are represented by the Nubians and Arabs). Interpopulation variability and genetic distances within other 46 populations of the Red Sea showed that although Rashaida and Beja people...
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Study of expression and maturation of mitochondrial oxidative phosphorylation system during mammal's prenatal period
Mrhálková, Andrea ; Hůlková, Martina (advisor) ; Ješina, Pavel (referee)
Postnatal adaptation of neonate to extrauterine life is among others dependent on maturation of mitochondrial oxidative phosphorylation system (OXPHOS). It depends on effective mitochondrial biogenesis during fetal developement. The inadequate capacity of mitochondrial OXPHOS system plays an important role in the neonatal mortality and morbidity. Therefore the study of mitochondrial biogenesis on molecular and biochemical level is important to improve the care of very premature neonates, especially critically ill premature neonates. This thesis has been worked out in The laboratory for study of mitochondrial disorders (Department of Pediatrics, 1st Faculty of Medicine, Charles University in Prague). The thesis is based on molecular genetic analyses, which are focused on characterisation of ATP synthase gene expression and on changes in mitochondrial DNA content during human and rat fetal development. The results provide the better insight into mitochondrial respectively ATP synthase biogenesis during human and rat fetal development.
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