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SzSA YearBook 2018/19

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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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