Borys Olifirov
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Borys Olifirov has a total of 32 co-authors. Here are the top co-authors by number of shared publications:
A. Okhrimenko
National Technical University of Ukraine “Igor Sikorsky Kyiv Polytechnic Institute,”, Kyiv, Ukraine
1 shared publication- Alastair G. B. Simpson
Department of Biology and Institute for Comparative Genomics Dalhousie University Halifax Nova Scotia Canada
1 shared publication - Anastasiia Horlova
European Molecular Biology Laboratory (EMBL), Heidelberg, Germany
1 shared publication - Dana Biruk1 shared publication
- Daniel J. Richter
Institut de Biologia Evolutiva (CSIC‐Universitat Pompeu Fabra) Barcelona Spain
1 shared publication - Daria Tashyreva
Institute of Evolutionary Biology, Faculty of Biology, University of Warsaw, Warsaw, Poland
1 shared publication
Latest Publications
- Open Access
Inverse relationship between mitochondrial and non-coding nuclear DNA content in free-living kinetoplastids
The evolution of genome size and eukaryotic genome organisation has puzzled evolutionary biologists for decades. Are differences in DNA content and protein-coding capacity of eukaryotic genomes a result of natural selection, or neutral processes? If they were shaped by natural selection, which features might be connected with these differences: cell volume, ecological strategy, availability of nutrients, etc.? Kinetoplastids are protists with compact nuclear genomes that almost entirely lack introns, but whose mitochondrial DNA content (kDNA) can rival that of their nuclei. We hypothesised that the reduction in non-protein coding nuclear DNA content during the evolution of kinetoplastids is connected with an increase in kDNA content: species with larger fractions of total cellular DNA that is allocated to kDNA will have concomitantly smaller fractions of non-coding DNA in the nuclear genome. We developed a framework for estimation of DNA content in both the mitochondria and nuclei from quantitative fluorescence microscopy data, and inferred the fraction of non-coding DNA in nuclear genomes based on the combination of transcriptomic and fluorescence imaging data. Across 10 genetically distant isolates from diverse free-living kinetoplastid lineages, there is indeed a trend towards a lower proportion of non-protein-coding nuclear DNA when kDNA proportion is higher relative to the total DNA in the cell. This observation is consistent with the hypothesis that in free-living kinetoplastids, mitochondrial and nuclear genomes might co-evolve in terms of their DNA content. This finding raises the possibility that natural selection acts on genome size evolution in kinetoplastids, and contributes evidence and methodology to address this question more broadly in eukaryotes.
Open AccessInverse relationship between mitochondrial and non-coding nuclear DNA content in free-living kinetoplastids
The evolution of genome size and eukaryotic genome organisation has puzzled evolutionary biologists for decades. Are differences in DNA content and protein-coding capacity of eukaryotic genomes a result of natural selection, or neutral processes? If they were shaped by natural selection, which features might be connected with these differences: cell volume, ecological strategy, availability of nutrients, etc.? Kinetoplastids are protists with compact nuclear genomes that almost entirely lack introns, but whose mitochondrial DNA content (kDNA) can rival that of their nuclei. We hypothesised that the reduction in non-protein coding nuclear DNA content during the evolution of kinetoplastids is connected with an increase in kDNA content: species with larger fractions of total cellular DNA that is allocated to kDNA will have concomitantly smaller fractions of non-coding DNA in the nuclear genome. We developed a framework for estimation of DNA content in both the mitochondria and nuclei from quantitative fluorescence microscopy data, and inferred the fraction of non-coding DNA in nuclear genomes based on the combination of transcriptomic and fluorescence imaging data. Across 10 genetically distant isolates from diverse free-living kinetoplastid lineages, there is indeed a trend towards a lower proportion of non-protein-coding nuclear DNA when kDNA proportion is higher relative to the total DNA in the cell. This observation is consistent with the hypothesis that in free-living kinetoplastids, mitochondrial and nuclear genomes might co-evolve in terms of their DNA content. This finding raises the possibility that natural selection acts on genome size evolution in kinetoplastids, and contributes evidence and methodology to address this question more broadly in eukaryotes.
- 7 September 2026
- Published by Springer Nature in Nature Genetics
- Vol. 58 (9) , 2073-2077
Training as infrastructure for biological data science in wartime Ukraine
- 7 September 2026
- Published by Springer Nature in Nature Genetics
- Vol. 58 (9) , 2073-2077
Training as infrastructure for biological data science in wartime Ukraine
- 12 May 2026
- Published by Elsevier in Biochemical and Biophysical Research Communications
- Vol. 822, 153895
Ceftriaxone has a similar effect on astrocytic and neuronal GLT-1 distribution after mild traumatic brain injury
- 12 May 2026
- Published by Elsevier in Biochemical and Biophysical Research Communications
- Vol. 822, 153895
Ceftriaxone has a similar effect on astrocytic and neuronal GLT-1 distribution after mild traumatic brain injury
- 19 August 2025
- Published by SIGMA (Symmetry, Integrability and Geometry: Methods and Application)
Comparison of Hippocalcin Translocation and Minor Phospholipid Distribution
Calcium ions $(\mathrm{Ca}^{2+})$ serve as vital second messengers in neurons, regulating numerous physiological processes. Neuronal calcium sensor $(\mathrm{NCS})$ proteins play a key role in this regulation by detecting changes in $\mathrm{Ca}^{2+}$ concentration in the cytosol and triggering downstream signalling. One such sensor, hippocalcin $(\mathrm{HPCA})$, binds $\mathrm{Ca}^{2+}$ and undergoes a reversible translocation to membranes, interacting with target proteins. Previous in vitro studies suggest that this translocation may be selective for membrane regions enriched with phosphatidylinositol 4,5-bisphosphate $(\mathrm{PIP}_2)$ [Biochem. J. 391 (2005), 231–238]. To further investigate this issue, we analysed the translocation of fluorescently-tagged $\mathrm{HPCA}$ in $\mathrm{HEK~} 293$ cells following a rapid homogeneous increase in $[\mathrm{Ca}^{2+}]_i$ induced by photolysis of caged $\mathrm{Ca}^{2+}$. In a separate series of experiments, we also recorded the distribution of $\mathrm{PIP}_2$ between the plasma membrane $(\mathrm{PM})$ and intracellular membranes $(\mathrm{IMs})$ using the fluorescently tagged $\mathrm{PH}$ domain of phospholipase $\mathrm{C}$, which has a high affinity for $\mathrm{PIP}_2$. Despite substantial variability in $\mathrm{PIP}_2$ localisation between $\mathrm{PM}$ and $\mathrm{IMs}$ in different cells, we found that $\mathrm{PIP}_2$ is generally more enriched in the intracellular membranes rather than in the plasma membrane. Notably, $\mathrm{HPCA}$ did not show a consistent preference for either compartment. These findings suggest that other unidentified factors contribute to the translocation and membrane targeting of $\mathrm{HPCA}$.- 19 August 2025
- Published by SIGMA (Symmetry, Integrability and Geometry: Methods and Application)
Comparison of Hippocalcin Translocation and Minor Phospholipid Distribution
Calcium ions $(\mathrm{Ca}^{2+})$ serve as vital second messengers in neurons, regulating numerous physiological processes. Neuronal calcium sensor $(\mathrm{NCS})$ proteins play a key role in this regulation by detecting changes in $\mathrm{Ca}^{2+}$ concentration in the cytosol and triggering downstream signalling. One such sensor, hippocalcin $(\mathrm{HPCA})$, binds $\mathrm{Ca}^{2+}$ and undergoes a reversible translocation to membranes, interacting with target proteins. Previous in vitro studies suggest that this translocation may be selective for membrane regions enriched with phosphatidylinositol 4,5-bisphosphate $(\mathrm{PIP}_2)$ [Biochem. J. 391 (2005), 231–238]. To further investigate this issue, we analysed the translocation of fluorescently-tagged $\mathrm{HPCA}$ in $\mathrm{HEK~} 293$ cells following a rapid homogeneous increase in $[\mathrm{Ca}^{2+}]_i$ induced by photolysis of caged $\mathrm{Ca}^{2+}$. In a separate series of experiments, we also recorded the distribution of $\mathrm{PIP}_2$ between the plasma membrane $(\mathrm{PM})$ and intracellular membranes $(\mathrm{IMs})$ using the fluorescently tagged $\mathrm{PH}$ domain of phospholipase $\mathrm{C}$, which has a high affinity for $\mathrm{PIP}_2$. Despite substantial variability in $\mathrm{PIP}_2$ localisation between $\mathrm{PM}$ and $\mathrm{IMs}$ in different cells, we found that $\mathrm{PIP}_2$ is generally more enriched in the intracellular membranes rather than in the plasma membrane. Notably, $\mathrm{HPCA}$ did not show a consistent preference for either compartment. These findings suggest that other unidentified factors contribute to the translocation and membrane targeting of $\mathrm{HPCA}$.- 1 January 2020
- Published by Springer Nature in Neurophysiology
- Vol. 52 (1) , 2-13
Hippocalcin Distribution between the Cytosol and Plasma Membrane of Living Cells
- 1 January 2020
- Published by Springer Nature in Neurophysiology
- Vol. 52 (1) , 2-13
Hippocalcin Distribution between the Cytosol and Plasma Membrane of Living Cells