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Role of phosphorylation in nuclear import of viral proteins and complexes
Pokorná, Karolína ; Forstová, Jitka (advisor) ; Roučová, Kristina (referee)
Replication of many different viruses occurs in the nucleus of the host cell. These viruses discovered ways how to overcome the nuclear membrane and often use cell transport machinery to transport their proteins and genome into the nucleus. For many viral proteins the timing of their nuclear import in order to secure correct viral replication is important. Regulated nuclear import also allows these proteins to perform several functions depending on their localization. Nuclear import of viral proteins and complexes can be regulated by phosphorylation. Phosphorylation can, for example, modulate affinity of proteins for importins or other cellular proteins. Phosphorylation can also cause conformational change, which can lead to unmasking of localization sequence.
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The role of the Smc5/6 complex in DNA viral infection
Protivová, Eliška ; Huerfano Meneses, Sandra (advisor) ; Pokorná, Karolína (referee)
The Smc5/6 complex is an eukaryotic protein complex that, together with Smc1/3 cohesin and Smc2/4 condensin, is involved in ensuring genome stability. It contributes to this by participating in the organization and maintenance of chromosomal structures as well as in the response to DNA damage. In addition, the Smc5/6 complex has been shown to play an important role in viral infection. This thesis focuses on the mechanisms of interaction of the Smc5/6 complex with viral DNA genomes, DNA intermediate genomes and viral proteins. In the case of HBV of the Hepadnaviridae family, Smc5/6 acts as a restriction factor. The same is true for HSV-1 of the Herpesviridae family, viruses of the Papillomaviridae family and HIV-1 of the Retroviridae family. An interaction of the Smc5/6 complex with the JC virus of the Polyomaviridae family has also been discovered. Nevertheless, the meaning of this interaction remains elusive. Some of the above-mentioned viruses can prevent this restriction. In detail, HBx protein of HBV mediates proteasomal degradation of the Smc5/6 complex or Vpr protein of HIV-1 induces degradation of the SLF2 protein, which is responsible for the Smc5/6 localization on HIV-1 DNA intermediate genomes. Keywords: Smc5/6 complex, DNA repair, ATPase, sumoylation, DNA viruses, viruses with a DNA...
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Interactions of mouse polyomavirus with Toll-like receptors
Pokorná, Karolína ; Forstová, Jitka (advisor) ; Němečková, Šárka (referee)
Toll-like receptors (TLRs) are important receptor family of innate immunity. They enable fast recognition of infection through so called pathogen associated molecular patterns (PAMPs). In this thesis, we studied interaction of mouse polyomavirus (MPyV) with TLRs of mouse embryonic fibroblasts (MEF cells). We observed that inhibition of TLR4 signaling abolished response of MEF cells to MPyV. This suggested that TLR4 plays a role in MEF cells recognition of MPyV. To detect response of MEF cell to MPyV, we measured IL-6 production by ELISA. Next, we investigated effect of TLR4 signalization on MPyV infection. Inhibition of TLR4 signaling with CLI-095 inhibitor did not affect number of infected cells. Presence of TLR4 antagonist, LPS-RS, led to significant decrease in quantity of infected cells 20 hours post infection. Decrease in number of infected cells was also observed in presence of LPS. Viral infection was also inhibited by TLR9 antagonist ODN 2088. We also investigated role of MAP kinases in MPyV infection. We tested, whether inhibition of selected MAP kinases would affect number of infected cells. Inhibition of kinase p38 did not affect infection. On the other hand, inhibition of MEK kinase or JNK resulted in decrease of number of cells infected by MPyV.
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Role of phosphorylation in nuclear import of viral proteins and complexes
Pokorná, Karolína ; Forstová, Jitka (advisor) ; Roučová, Kristina (referee)
Replication of many different viruses occurs in the nucleus of the host cell. These viruses discovered ways how to overcome the nuclear membrane and often use cell transport machinery to transport their proteins and genome into the nucleus. For many viral proteins the timing of their nuclear import in order to secure correct viral replication is important. Regulated nuclear import also allows these proteins to perform several functions depending on their localization. Nuclear import of viral proteins and complexes can be regulated by phosphorylation. Phosphorylation can, for example, modulate affinity of proteins for importins or other cellular proteins. Phosphorylation can also cause conformational change, which can lead to unmasking of localization sequence.
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