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SZENT-GYÖRGYI JUNIOR MENTORS<br />
BALÁZS VEDELEK<br />
University of Szeged,<br />
Department of Biochemistry and MolecularBiology<br />
Address: Közép fasor 52., H-6726 Szeged, Hungary<br />
RESEARCH AREA<br />
Telomeres are nucleoprotein complexes responsible for<br />
the protection of chromosome integrity. Telomeres hide<br />
the ends of the chromosomes from DNA repair mechanism<br />
to prevent chromosome fusions. Telomeres also buffer the<br />
’end replication problem’ by the telomerase enzyme, which<br />
can elongate the chromosomes ends. In human somatic<br />
cells the telomerase is inactive; the chromosomes are<br />
continuously shortening, which results in the senescence of<br />
the cells. In tumours however the telomerase is reactivated<br />
and provides the possibility of unlimited cell divisions. In<br />
our lab we study the mechanisms behind telomerase gene<br />
activation in tumours.<br />
TECHNIQUES AVAILABLE IN THE LAB<br />
SELECTED PUBLICATIONS<br />
Sike, A., Nagy, E., Vedelek, B., et al. (2014) mRNA levels<br />
of related Abcbgenes change opposite to each other<br />
upon histonedeacetylase inhibition in drug-resistant<br />
rathepatoma cells. PLoSOne. 2014;9(1): e84915. Published<br />
2014 Jan 7. doi:10.1371/journal.pone.0084915<br />
Vedelek, B., Blastyák, A., Boros, I.M. (2015) Cross-Species<br />
Interaction between Rapidly Evolving Telomere-Specific<br />
Drosophila Proteins. PLoSOne. 2015;10(11): e0142771.<br />
Published 2015 Nov 13. doi:10.1371/journal.pone.0142771<br />
Pahi, Z., Borsos, B.N., Vedelek, B., et al. (2017) TAF10 and<br />
TAF10b partially redundant roles during Drosophila<br />
melanogastermorphogenesis Transcription. 2017;8(5):<br />
297-306.<br />
IDNA extraction (blood and tissue samples), DNA<br />
quantitation (NanoDrop spectrophotometer and Quantus<br />
fluorometer), primer design, different PCR techniques<br />
(Repeat-Primed PCR, Real-Time PCR, Digital PCR), agarose gel<br />
electrophoresis, Sanger sequencing and amplicon fragment<br />
length analysis. Next generation sequencing (target region/<br />
panel and exome sequencing) and bioinformatic analysis<br />
of NGS data. Clinical and mutation database management<br />
and variant effect prediction.<br />
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