Investigation of the physiological role of dUTPase

The dUTPase enzyme has a dual role in maintaining genomic integrity. On one hand, it sanitizes the nucleotide pool from dUTP regulating the cellular dUTP/dTTP level, on the other hand, it provides a substrate for thymidylate synthase for de novo thymidylate biosynthesis. When dUTP accumulates excessively, it can be incorporated into the DNA. Uncontrolled incorporation of dUTP can induce a futile cycle of the repair process, leading to single- and double-stranded DNA breaks and cell death. In mammalian cells, dUTPase is present in two isoforms, one of them is nuclear and the other is mitochondrial/cytoplasmic. Both isoforms of dUTPase are encoded by the DUT gene and are generated by alternative 5` splicing and alternative promoter usage. The mitochondrial isoform (DUT-M) differs in the first exon from the nuclear isoform (DUT-N), as it contains the mitochondrial targeting sequence. Nucleocytoplasmic localization of DUT-N is regulated by phosphorylation on a serine residue (Ser11) adjacent to the NLS. Phosphorylation occurs in the M phase by cyclin dependent kinase 1 (CDK1) and it leads to the exclusion of the enzyme from the nucleus during mitosis [Doi: 10.1107/S0907444913023354, Doi: 10.4161/15384101.2014.960740].

To investigate the role of dUTPase during embryonic development, we knocked out the Dut gene in mouse using CRISPR/Cas9 technique. We showed that dUTPase is essential for embryonic development since early Dut -/- embryos reach the blastocyst stage, however, they die shortly after implantation [Doi: 10.3390/biom9040136].

In mouse, the mRNA expression of the different dUTPase isoforms was not described in the literature. Therefore, we developed and optimized an RT-qPCR method to characterize the isoform-specific expression patterns of dUTPase in adult mouse tissues [Doi: 10.1002/2211-5463.12654]. We are also investigating the development specific expression pattern of the dUTPase isoforms in embryonic, 2-week-old, 4-week-old, 10-week-old and 13-month-old mouse tissues. We characterized the protein localisation of dUTPase in adult mouse brain.

In human cells, high-throughput sequencing studies predicted the putative presence of two additional isoforms of dUTPase, termed as DUT-3 and DUT-4. Sequence databases suggested that the DUT-3 does not contain any localisation signal, thus it is most probably retained in the cytosol. The DUT-4 was predicted to closely resemble the DUT-N isoform, only differing in a few amino acids at the N-terminus. To measure the gene expression of the dUTPase isoforms with RT-qPCR, we identified novel suitable reference genes (SNW1 and CNOT4) with low expression variability among human cancer and normal cell lines [Doi: 10.1038/s41598-021-98869-x]. We developed and optimized an RT-qPCR method to characterize the mRNA expression of the dUTPase isoforms in 13 cancer and 7 normal human cell lines. We found that the mRNA expression of the DUT-N is the most abundant, while the expression of the DUT-M and DUT-3 is similar, although the DUT-4 isoform shows a different pattern and has the lowest expression level. A strong correlation between the expression levels of DUT-M and DUT-3 suggests that these two isoforms may share the same promoter. Taken together our results indicate that the cellular dUTPase supply may also be provided in the cytoplasm and starvation stress induced expression changes are cell line dependent. In addition, we have successfully exposed the novel DUT-3 isoform on protein level using western blot analysis [Doi: 10.1038/s41598-023-32970-1].

dUTPase role

Relative normalized gene expression data for the dUTPase targets and correlation analysis of the Cq values.
Rácz, GA., Nagy, N., Vértessy BG. et al., Discovery of two new isoforms of the human DUT gene. Sci Rep (2023) Doi: 10.1038/s41598-023-32970-1


Physiological consequences and potential role of uracil substitution in genomes of model organisms

Conventionally, deoxyuridine incorporation into DNA is regarded to represent erroneous lesions, however chemical features of the uracil base does not show a remarkable difference from thymine except from a single methyl group at  the 5th position of the pyrimidine ring. As the balance of the cellular nucleotide pool is deterministic in the quality of DNA synthesis, dUTPase catalyzing the hydrolysis of dUTP is a major player in the maintenance of this balance and uracil-free genome. Our research is focused on the genome metabolism of uracil substituted DNA in the framework of a new paradigm, suggesting that deoxyuridine lesions might assign unique fate for DNA in special cases. These cases are extensively studied recently by a set of research groups including ours.  The special instances in which the presence of uracil was verified to have a unique role are the following:

  • Immunoglobuline gene diversification
  • Transcriptional regulation
  • HIV life cycle
  • and developmental biology.

We focus on some of the above mentioned or other examples of uracil-DNA mediated cellular events. We employ this paradigm on model organisms such as mammalian or tumor-derived cell lines and Drosophila melanogaster. The physiological role of uracil substituted DNA is studied either genome scale by methods of molecular and cell biology. In Drosophila, complex developmental consequences are also examined in our lab.


Interconnections of thymineless cell death with cellular signaling pathways

Almost all organisms employ a cluster of metabolic enzymes devoted for thymine biosynthesis in order to utilize thymine bases instead of uracil in their genome. The medical significance of this metabolic pathway is marked by the fact that nearly one-third of anti-cancer drugs used in clinics are targeted against thymidilate biosynthesis (such as fluoro-pyrimidines, anti folates) potentially inducing the so called thymine-less cell death. Personalized medicine aiming to minimize side effects and maximize the efficiency of chemotherapies requires prior knowledge about the characteristics of tumorous cells in order to predict the desired effect of a particular drug. Detailed mapping of protein networks participating or being affected by thymine-less cell death help us to estimate the receptivity of tumorous cells for drugs targeting thymidilate biosynthesis. We would like to contribute for this knowledge through our research that includes the characterization of thymine-less cell death. We especially aim to explore the involvement of dUTPase in the cellular process of thymine-less cell death. 

Study of a molecular switch: Structural and molecular biological research on the Staphylococcus aureus pathogenicity island regulation

The bacterial genom frequently contains mobile genetic elements, which can replicate more or less independently from the bacterial chromosome. Some of these are phage related such as the pathogenicity islands (PIs), which have significant biomedical importance, since these are responsible for horizontal transfer of several toxins and virulence factors (for eg. the toxic shock syndrome).

Phage mediated mobilisation of some Staphylococcus aureus PIs are induced by formation of a repressor:derepressor complex of the Staphylococcal repressor protein (Stl) with a phage-related dUTPase. Studying the detailed mechanism of this interaction can provide much needed deep insight into bacterial gene expression regulation pathways, and potentially facilitates the design of new anti-bacterial compounds. In this project we investigate this system using various in vitro techniques ( native gel electrophoresis, electrophoretic mobility shift assay, steady-state and transient kinetics, VIS and fluorescence spectroscopy, mass spectrometry and X-ray crystallography).

dNTP metabolism in genotoxic stress tolerance

Cells maintain a fine-tuned concentration balance in the pool of deoxyribonucleoside 5’-triphosphates (dNTPs). The perturbation of this balance results in "mutator" phenotypes characterized by increased mutation frequencies. Genotoxic stress acts upon the dNTP pool directly and also via the SOS response to DNA damage. Our model is Mycobacterium smegmatis that shares the DNA metabolic and repair pathways with the tuberculosis bacterium, Mycobacterium tuberculosis. This intracellular pathogen is exposed to harsh genotoxic conditions by the host immune defense against them. It is therefore of major importance for these bacteria to develop strategies for the adaptation to genotoxic environmental conditions. We hope to understand how the changes in the dNTP pool possibly promote drug resistance as part of the adaptation to genotoxic stress.

Design of novel molecular tools

Cells maintain a fine-tuned balance of deoxyribonucleoside 5′-triphosphates (dNTPs). The perturbation of this balance results in increased mutation frequencies, replication arrest and may promote cancer development. The size and constitution of the cellular dNTP pool is therefore an important indication for several processes with poor outcome for the cell. To determine cellular dNTP pools, radioactive and mass spectrometry-based assays have long been available. These are precise and sensitive, but tedious and/or hardly available for most researchers. An easily accessible, TaqMan-like dNTP quantitation assay was finally published. But unfortunately, it failed to produce reliable data in most biological samples. Our group identified and overcome the difficulties of this assay and published a new kinetics-based analysis method. We automated this analysis process in the nucleoTIDY software thus offering an easily accessible and high-throughput method.

Our new technique greatly accelerated different key projects in the lab involving dNTP metabolism. We identified the effects of various antibiotics on Mycobacterium smegmatis dNTP pools as part of a hot topic investigation: finding how antibiotic resistance genes develop. Also, we use our method for the determination of the dNTP pool in various developmental stages of the causative agent of malaria infection, Plasmodium falciparum. We also study dNTP levels in zebrafish embryos at different developmental stages.

 Szabo Suranyi NAR


Maintenance of genomic integrity in the malaria parasite Plasmodium falciparum

Our research focuses on the maintenance of genomic integrity and characterization of molecular background of the quick adaptability of the malaria parasite Plasmodium falciparum. Previously, we showed the constant presence of uracil, a non-canonical base in the genomic DNA of P. falciparum throughout its intraerythrocytic life cycle. This phenomenon raised the question of the involvement of DNA repair pathways in the genetic variability of the parasite. We want to further elaborate on the molecular mechanism behind the exceptional ability of the parasites to emerge resistance in an accelerated rate.

We primarily focus on the base excision repair (BER) pathway of the Plasmodium falciparum parasite. The BER pathway is well-known in other eukaryotic organisms, however it remains poorly characterized in P. falciparum. Our goal is to characterize the proteins that are responsible for the initiation of the BER pathway known as DNA glycosylases. The two non‑canonical bases that could be of outmost interest are uracil and 8-oxo-guanine and their respective glycosylases, uracil DNA-glycosylase (UNG) and 8-oxo-guanine-DNA-glycosylase. We want to characterize the impact of the CRISPR-Cas9-based knockout of these proteins on the mutation rate and whether it leads to in increased rate of emerging resistance. Furthermore, we want to follow its localization and expression throughout the intraerythrocytic life cycle of the parasite.

Additionally, our other objective is to determine the amount of deoxynucleotides (dNTPs) throughout the life cycle. The maintenance of genomic integrity heavily relies on the ratio of dNTPs. A perturbed dNTP pool leads to mismatches during the DNA replication, as the high-processivity of DNA polymerase can overcome the lack of complementarity. It is especially notable in case of dUTP and dTTP, as their respective bases uracil and thymine only differ in a single methyl-group. UMP is an important precursor of both dCTP and dTTP, therefore its presence is inevitable. Moreover, in Plasmodium falciparum the biosynthesis of dTMP requires the synthesis dUTP, which could potentially lead to the incorporation of dUTP during replication. By elucidating the dynamics of dNTP biosynthesis, we could understand the key steps that could be exploited as antimalarial drug targets and what is their impact on genomic integrity under drug pressure.


Babai, R., Izrael, R. & Vértessy, B.G. Characterization of the dynamics of Plasmodium falciparum deoxynucleotide-triphosphate pool in a stage-specific manner. Sci Rep (2022).

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Genome Metabolism and Biostruct Laboratory

Budapest University of Technology, Ch building
Szt. Gellért square 4.

RCNS Institute of Enzymology
Magyar tudosok korutja 2.