Informacja

Drogi użytkowniku, aplikacja do prawidłowego działania wymaga obsługi JavaScript. Proszę włącz obsługę JavaScript w Twojej przeglądarce.

Wyszukujesz frazę "DNA transfer" wg kryterium: Temat


Wyświetlanie 1-9 z 9
Tytuł:
Odyssey of Agrobacterium T-DNA.
Autorzy:
Ziemienowicz, Alicja
Tematy:
Agrobacterium
DNA transfer
T-DNA
virulence
Pokaż więcej
Wydawca:
Polskie Towarzystwo Biochemiczne
Powiązania:
https://bibliotekanauki.pl/articles/1044091.pdf  Link otwiera się w nowym oknie
Opis:
Agrobacterium tumefaciens, a plant pathogen, is characterized by the unique feature of interkingdom DNA transfer. This soil bacterium is able to transfer a fragment of its DNA, called T-DNA (transferred DNA), to the plant cell where T-DNA is integrated into the plant genome leading to "genetic colonization" of the host. The fate of T-DNA, its processing, transfer and integration, resembles the journey of Odysseus, although our hero returns from its long trip in a slightly modified form.The soil bacterium, Agrobacterium tumefaciens, is a plant pathogen responsible for tumor induction on dicotyledonous plants due to its ability to transfer DNA to the plant cell (reviewed in: de la Cruz & Lanka, 1998; Gelvin, 2000; Hansen & Chilton, 1999; Lartey & Citovsky, 1997; Rossi et al., 1998; Zupan & Zambryski, 1997). In biotechnology this ability is widely used for plant transformation. During tumor induction Agrobacterium attaches to plant cells and then transfers part of its DNA to some of these cells. The transferred DNA (T-DNA) which resides on a large Ti (tumor inducing) plasmid, is processed within the bacterium and is exported to the plant where it becomes integrated into the plant genome (reviewed in: Sheng & Citovsky, 1996; Tinland & Hohn, 1995; Tinland, 1996). Proteins encoded by the virulence (vir) region of the Ti plasmid regulate T-DNA processing and transfer. Phenolic compounds derived from a wounded plant cell wall induce expression of the vir region genes. Virulence proteins recognize 25 bp imperfect direct repeats (border sequences) that define the T-DNA. In the presence of VirD1 protein, VirD2 cleaves the border sequence in a site- and strand-specific manner and subsequently becomes covalently attached to the 5' end of the nicked DNA. The nicked DNA is then displaced from the plasmid producing single-stranded T-DNA. The T-DNA-VirD2 complex and the VirE2 protein are believed to be transferred to the plant through a pilus-like structure containing VirB and VirD4 proteins. In the plant cell, T-DNA becomes coated with the single-stranded DNA-binding protein, VirE2. The T-DNA-protein complex is imported into the nucleus where the T-DNA is integrated into the nuclear genome. Expression of genes located on T-DNA leads to the formation of proteins involved in the production of auxins and cytokinins. These plant hormones cause the tumorous phenotype that is characterized by the ability of the plant cells to proliferate limitlessly and autonomously even in the absence of added phytohormones. Crown gall tumors are characterized by the production of opines (amino-acid derivatives). The biosynthesis of opines is catalyzed by opine synthases, which are encoded by the T-DNA. Opines formed in the tumors can be metabolized by the tumorigenic agrobacteria, but not by most of the other soil organisms. Thus, Agrobacterium creates for itself a favorable niche by genetic modification of plant cells, a process called "genetic colonization". All stages of this colonization, including chemotaxis, attachment, induction of virulence region, processing of T-DNA, T-DNA transfer, T-DNA integration, expression of T-DNA genes and changes in the plant phenotype, will be discussed in the following chapters. This will be an odyssey of T-DNA that leaves the Agrobacterium cell in the form of nucleic acid and returns from its journey in the form of opines, derivatives of amino acids (Fig. 1).
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Direct in vivo transfer of plasmid DNA into murine tumors: Effects of endotoxin presence and transgene localization.
Autorzy:
Budryk, Magdalena
Cichoń, Tomasz
Szala, Stanisław
Tematy:
DNA transfer in vivo
endotoxin
myofibroblasts
naked DNA
Pokaż więcej
Wydawca:
Polskie Towarzystwo Biochemiczne
Powiązania:
https://bibliotekanauki.pl/articles/1044111.pdf  Link otwiera się w nowym oknie
Opis:
The purpose of this study was to investigate the effect of endotoxin presence in plasmid DNA preparations on the efficiency of transfection achieved in vivo with B16(F10) and Renca tumors and to determine transgene localization. Our data show that endotoxin markedly decreases the efficiency of transfection. Furthermore, the transgene transferred in vivo can be found in both neoplastic and normal (most likely myofibroblast) cells lying in proximity of the administration site.
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Profilowanie genetyczne śladów daktyloskopijnych - problem wtórengo transferu materiału
Genetic profiling from fingerprints - the issue of secondary DNA transfer
Autorzy:
Pająk, Katarzyna
Wierzchosławski, Rafał
Tematy:
śladowe ilości DNA
wtórny transfer DNA
ślady daktyloskopijne
profilowanie DNA
trace DNA
secondary DNA transfer
latent fingerprints
DNA profiling
Pokaż więcej
Wydawca:
Centralne Laboratorium Kryminalistyczne Policji
Powiązania:
https://bibliotekanauki.pl/articles/499824.pdf  Link otwiera się w nowym oknie
Opis:
Rozwój technik molekularnych umożliwił pozyskiwanie profili genetycznych ze śladowych ilości materiału biologicznego. Od połowy lat 90. coraz częściej podejmowane są próby namnażania DNA z odcisków palców. Dotychczasowe badania dowiodły, że wykorzystanie technik ujawniania śladów daktyloskopijnych nie wyklucza późniejszej analizy genetycznej. Coraz liczniejsze są jednak dowody na to, iż narzędzia stosowane do ujawniana śladów mogą akumulować materiał genetyczny i prowadzić do wtórnego transferu DNA, skutkującego zanieczyszczeniem materiału dowodowego. Konieczne wydaje się więc wprowadzenie procedur pozwalających zminimalizować ryzyko zanieczyszczenia śladu, tak aby metody identyfikacji daktyloskopijnej nie kolidowały z metodami identyfikacji genetycznej.
The improvement of molecular biology techniques allowed the obtaining of genetic profiles from minute amounts of biological material. Since the mid-90s DNA typing of latent fingerprints became a common procedure in forensic casework. Numerous studies have shown that the fingerprint detection techniques do not preclude further genetic identification. However, there is a growing evidence that the tools used in the dactyloscopic visualization can accumulate genetic material and become a source of secondary DNA transfer, resulting in contamination of traces. Therefore, it seems necessary to develop procedures that minimize the risk of evidence contamination, so that the dactyloscopic methods do not interfere with genetic identification.
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Charge transfer in DNA and repair of oxidative damage
Autorzy:
Męczyńska, S.
Szumiel, I.
Tematy:
charge transfer in DNA
DNA repair
oxidative base damage
base damage excision
4Fe-4S cluster
MutY glycosylase
photolyase
Pokaż więcej
Wydawca:
Instytut Chemii i Techniki Jądrowej
Powiązania:
https://bibliotekanauki.pl/articles/146454.pdf  Link otwiera się w nowym oknie
Opis:
The possibility of a biological role of an unusual function of DNA sequences is discussed, namely, signaling by charge transfer within chromatin. Although a general conclusion on its biological significance is premature, the idea of charge transfer accompanying repair of some types of oxidative DNA damage is based on sound experimental data. Both physical and chemical experiments reviewed here provided results indicating that DNA duplex under certain conditions (among them – hydration) – can behave as narrow band gap semiconductor. With the use of model molecules it was shown that charge transfer most probably occurs by hopping between guanine residues and tunneling through thymine-adenine (TA) base pairs. Charge transfer is nucleotide sequence and distance dependent. Furthermore, the pi-stacked base pairs must be perfectly matched to mediate charge transfer and in a damaged double helix this condition is not fulfilled. Hence, the possibility that charge transfer takes place in oxidatively damaged DNA after UV or X-irradiation and it becomes interrupted by mismatched base pairs, thus signaling the mismatch or strand break to the repair machinery. Function of base damage repair enzymes which contain [4Fe-4S] clusters is discussed in this context.
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Exploring the Synergies of Single-Molecule Fluorescence and 2D Materials Coupled by DNA
Autorzy:
Kamińska, Izabela
Richter, Lars
Manzanares-Palenzuela, Lorena
Szalai, Alan M.
Tinnefeld, Philip
Wydawca:
Wiley Online Library
Cytata wydawnicza:
Richter, L., Szalai, A. M., Manzanares‐Palenzuela, C. L., Kamińska, I., & Tinnefeld, P. (2023). Exploring the Synergies of Single‐Molecule Fluorescence and 2D Materials Coupled by DNA. Advanced Materials, 35 (41), 2303152. https://doi.org/10.1002/adma.202303152
Opis:
The world of 2D materials is steadily growing, with numerous researchers attempting to discover, elucidate, and exploit their properties. Approaches relying on the detection of single fluorescent molecules offer a set of advantages, for instance, high sensitivity and specificity, that allow the drawing of conclusions with unprecedented precision. Herein, it is argued how the study of 2D materials benefits from fluorescence-based single-molecule modalities, and vice versa. A special focus is placed on DNA, serving as a versatile adaptor when anchoring single dye molecules to 2D materials. The existing literature on the fruitful combination of the two fields is reviewed, and an outlook on the additional synergies that can be created between them provided.
Dostawca treści:
Repozytorium Centrum Otwartej Nauki
Artykuł
Tytuł:
DNA methylation, histone modifications and behaviour of AKAP95 during mouse oocyte growth and upon nuclear transfer of foreign chromatin into fully grown prophase oocytes
Autorzy:
Polański, Zbigniew
Tomasik, Grzegorz
Hoffmann, Steffen
Opis:
The poor efficiency of mammalian cloning is due to inappropriate/incomplete epigenetic reprogramming of the donor chromatin. As the success in reprogramming of the donor nucleus may require activity of similar mechanisms which reprogram the chromatin in the course of gametogenesis, we decided to follow the status of some epigenetic markers in the late phase of oogenesis in mice, i.e. in prophase oocytes during their growth and after completion of the growth phase. Our analysis reveals an increase in the level of global DNA methylation starting in oocytes with diameters around 60/mu m which was further elevated until completion of oocyte growth. A similar increase was observed in respect to the acetylation of histone H4. On the other hand, the methylation of histone H4 Arg3 was constantly high until the end of oocyte growth, although it differed between fully grown oocytes depending on the type of spatial chromatin organization. We have also studied the AKAP95 protein which was abundant at earlier stages but decreased in fully grown oocytes according to changes in their chromatin organization. The nuclear transfer of different types of donor nuclei with hypomethylated DNA into fully grown prophase oocytes did not increase the global level of methylation of transferred foreign chromatin, regardless if the recipient oocyte was devoid of its own nucleus or its nucleus was left intact. This suggests a major problem in the ability of recipient oocytes to modify donor DNA methylation.
Dostawca treści:
Repozytorium Uniwersytetu Jagiellońskiego
Artykuł
Tytuł:
Applications of recent advances at the Institute of Grassland and Environmental Research in cytogenetics of the Lolium-Festuca complex
Autorzy:
Humphreys, M W
Thomas, H M
King, I P
Morgan, W G
Meredith, M R
Harper, J A
Humphreys, M O
Bettany, A J E
Dalton, S J
James, A R
Ougham, H J
Thomas, H
Tematy:
RNA
in situ
tissue culture
gene transfer
chromosome segment
anther culture
androgenesis
plant breeding
introgression mapping
fluorescence
hybridization
Lolium-Festuca complex
drought resistance
gene isolation
tetraploid hybrid
DNA
meiosis
grass
chromosome behaviour
Pokaż więcej
Wydawca:
Polska Akademia Nauk. Czytelnia Czasopism PAN
Powiązania:
https://bibliotekanauki.pl/articles/2046675.pdf  Link otwiera się w nowym oknie
Opis:
Recent advances at Institute of Grassland and Environmental Research (Aberystwyth, U.K.) in cytogenetics of the Lolium/Festuca complex places us in the advantageous position of being able to map genes of agronomic importance onto chromosome arms using fluorescence in situ hybridization (FISH). The ability to physically map genes leads to the capability for "dissecting" quantitative traits into their different components and will lead to better understanding of the complex physiological processes involved and the identification of their genetic control. By tagging genes of interest, using molecular and morphological markers, it will be possible to select and combine suites of desirable genes in a single genotype and thus produce novel cultivars by conventional breeding procedures. Programmes for introgression depend on the relationships between species and on levels of chromosome pairing. Phylogenetic relationships within the Lolium/Festuca complex are being determined using both genomic in situ hybridization (GISH) and FISH. With recent advances in genetic manipulation within the Lolium/Festuca complex, opportunities now arise for gene transfer from Lolium and Festuca species into other important agricultural crops.
Dostawca treści:
Biblioteka Nauki
Artykuł
    Wyświetlanie 1-9 z 9

    Ta witryna wykorzystuje pliki cookies do przechowywania informacji na Twoim komputerze. Pliki cookies stosujemy w celu świadczenia usług na najwyższym poziomie, w tym w sposób dostosowany do indywidualnych potrzeb. Korzystanie z witryny bez zmiany ustawień dotyczących cookies oznacza, że będą one zamieszczane w Twoim komputerze. W każdym momencie możesz dokonać zmiany ustawień dotyczących cookies