Michal J. Dabrowski

Dr. Michal J. Dabrowski

Institute of Computer Science, Polish Academy of Sciences, Computational Biology Lab, PL-01248 Warsaw, Poland
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Research Focus & Metrics

Academic Career Length

19Years (2008-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 November 2013 in Conservation Genetics
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Journal Article
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AMAndre E. Moura
Andre E. Moura
ETElena Tsingarska
Elena Tsingarska
MDMichal J. Dabrowski
Michal J. Dabrowski
SCSylwia Czarnomska
Sylwia Czarnomska
BJBogumiła Jędrzejewska
Bogumiła Jędrzejewska
MPMalgorzata Pilot
Malgorzata Pilot
European wolf (Canis lupus) populations have suffered extensive decline and range contraction due to anthropogenic culling. In Bulgaria, although wolves are still recovering from a severe demographic bottleneck in the 1970s, hunting is allowed with few constraints. A recent increase in hunting pressure has raised concerns regarding long-term viability. We thus carried out a comprehensive conservation genetic analysis using microsatellite and mtDNA markers. Our results showed high heterozygosity levels (0.654, SE 0.031) and weak genetic bottleneck signals, suggesting good recovery since the 1970s decline. However, we found high levels of inbreeding (F IS = 0.113, SE 0.019) and a N e/N ratio lower than expected for an undisturbed wolf population (0.11, 95 % CI 0.08–0.29). We also found evidence for hybridisation and introgression from feral dogs (C. familiaris) in 10 out of 92 wolves (9.8 %). Our results also suggest admixture between wolves and local populations of golden jackals (C. aureus), but less extensive as compared with the admixture with dogs. We detected local population structure that may be explained by fragmentation patterns during the 1970s decline and differences in local ecological characteristics, with more extensive sampling needed to assess further population substructure. We conclude that high levels of inbreeding and hybridisation with other canid species, which likely result from unregulated hunting, may compromise long-term viability of this population despite its current high genetic diversity. The existence of population subdivision warrants an assessment of whether separate management units are needed for different subpopulations. Our study highlights conservation threats for populations with growing numbers but subject to unregulated hunting.

Verified
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MDMichal J. Dabrowski
Michal J. Dabrowski
BWBartosz Wojtas
Bartosz Wojtas
During the last two decades, several international consortia have been established to unveil the molecular background of human cancers including gliomas. As a result, a huge outbreak of new genetic and epigenetic data appeared. It was not only shown that gliomas share some specific DNA sequence aberrations, but they also present common alterations of chromatin. Many researchers have reported specific epigenetic features, such as DNA methylation and histone modifications being involved in tumor pathobiology. Unlike mutations in DNA, epigenetic changes are more global in nature. Moreover, many studies have shown an interplay between different types of epigenetic changes. Alterations in DNA methylation in gliomas are one of the best described epigenetic changes underlying human pathology. In the following work, we present the state of knowledge about global DNA methylation patterns in gliomas and their interplay with histone modifications that may affect transcription factor binding, global gene expression and chromatin conformation. Apart from summarizing the impact of global DNA methylation on glioma pathobiology, we provide an extract of key mechanisms of DNA methylation machinery.

28 October 2013 in Molecular Ecology Resources
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MDMichal J. Dabrowski
Michal J. Dabrowski
MPMalgorzata Pilot
Malgorzata Pilot
MKM Kruczyk
M Kruczyk
MŻM Żmihorski
M Żmihorski
HUH M Umer
H M Umer
JGJ Gliwicz
J Gliwicz

8 April 2014 in PLOS ONE
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MPMalgorzata Pilot
Malgorzata Pilot
MDMichal J. Dabrowski
Michal J. Dabrowski
VHVahram Hayrapetyan
Vahram Hayrapetyan
EYEduard G. Yavruyan
Eduard G. Yavruyan
NKNatia Kopaliani
Natia Kopaliani
WBWiesław Bogdanowicz
Wiesław Bogdanowicz
Despite continuous historical distribution of the grey wolf (Canis lupus) throughout Eurasia, the species displays considerable morphological differentiation that resulted in delimitation of a number of subspecies. However, these morphological discontinuities are not always consistent with patterns of genetic differentiation. Here we assess genetic distinctiveness of grey wolves from the Caucasus (a region at the border between Europe and West Asia) that have been classified as a distinct subspecies C. l. cubanensis. We analysed their genetic variability based on mtDNA control region, microsatellite loci and genome-wide SNP genotypes (obtained for a subset of the samples), and found similar or higher levels of genetic diversity at all these types of loci as compared with other Eurasian populations. Although we found no evidence for a recent genetic bottleneck, genome-wide linkage disequilibrium patterns suggest a long-term demographic decline in the Caucasian population – a trend consistent with other Eurasian populations. Caucasian wolves share mtDNA haplotypes with both Eastern European and West Asian wolves, suggesting past or ongoing gene flow. Microsatellite data also suggest gene flow between the Caucasus and Eastern Europe. We found evidence for moderate admixture between the Caucasian wolves and domestic dogs, at a level comparable with other Eurasian populations. Taken together, our results show that Caucasian wolves are not genetically isolated from other Eurasian populations, share with them the same demographic trends, and are affected by similar conservation problems.

15 June 2021 in Nature Communications
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KSKarolina Stępniak
Karolina Stępniak
MMMagdalena A. Machnicka
Magdalena A. Machnicka
JMJakub Mieczkowski
Jakub Mieczkowski
AMAnna Macioszek
Anna Macioszek
BWBartosz Wojtas
Bartosz Wojtas
BWBartek Wilczynski
Bartek Wilczynski
Chromatin structure and accessibility, and combinatorial binding of transcription factors to regulatory elements in genomic DNA control transcription. Genetic variations in genes encoding histones, epigenetics-related enzymes or modifiers affect chromatin structure/dynamics and result in alterations in gene expression contributing to cancer development or progression. Gliomas are brain tumors frequently associated with epigenetics-related gene deregulation. We perform whole-genome mapping of chromatin accessibility, histone modifications, DNA methylation patterns and transcriptome analysis simultaneously in multiple tumor samples to unravel epigenetic dysfunctions driving gliomagenesis. Based on the results of the integrative analysis of the acquired profiles, we create an atlas of active enhancers and promoters in benign and malignant gliomas. We explore these elements and intersect with Hi-C data to uncover molecular mechanisms instructing gene expression in gliomas.

13 May 2016 in Human Mutation
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HUHusen M. Umer
Husen M. Umer
MCMarco Cavalli
Marco Cavalli
MDMichal J. Dabrowski
Michal J. Dabrowski
KDKlev Diamanti
Klev Diamanti
MKMarcin Kruczyk
Marcin Kruczyk
CWClaes Wadelius
Claes Wadelius