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Inhaltsbereich
Mark Wossidlo
Ap. Prof. Dr. rer. nat. Mark WossidloGroup Leader

Center for Anatomy and Cell Biology (Division of Cell and Developmental Biology)
ORCID: 0000-0002-3184-0753
T +43 1 40160 37717
mark.wossidlo@meduniwien.ac.at

Further Information

Keywords

DNA Methylation; Embryo, Mammalian; Embryonic Stem Cells; Epigenomics

Research group(s)

  • Epigenetic Reprogramming in the Wossidlo lab
    Head: Mark Wossidlo
    Research Area: We are interested in the embryo intrinsic epigenetic reprogramming that drives early preimplantation development and the establishment of cellular potency.
    Members:
    Kristeli Eleftheriou
    Mark Wossidlo
    Julia Arand

Research interests

In early mammalian development, a little miracle is happening with every start of a new life. Here, shortly after fertilization, mammalian embryogenesis is characterized by dramatic epigenetic remodeling of the oocyte and sperm chromatin. This epigenetic reprogramming of the highly specialized egg and sperm epigenomes gives rise to the toti- and pluripotent blastomeres of preimplantation embryos, which are capable of generating all cell types needed to form a new life. Most intriguingly, the genomes of early embryos undergo genome-wide DNA methylation (5-methyl-cytosine, 5mC) changes. Recent work suggests that DNA methylation reprogramming is an essential mechanism in early embryogenesis and the establishment of toti- and pluripotency.

Our group aims to elucidate the embryo intrinsic epigenetic reprogramming that drives early preimplantation development and the establishment of cellular potency. We seek to understand the influence of epigenetic reprogramming on the establishment of toti-/pluripotency in vivo. Insights from epigenomic changes in early embryogenesis in vivo will identify key factors for the generation of toti- and pluripotent cells in vitro, which will translate into the improved generation of human stem cells for regenerative medicine and treatment of common human diseases.

Techniques, methods & infrastructure

We use mouse embryos and embryonic stem cells in combination with novel epigenomic editing methods to investigate the impact of epigenetic changes and inter-/transgenerational inheritance of epimutations on development and cellular potency.

Selected publications

  1. Arand, J. et al., 2021. Tet enzymes are essential for early embryogenesis and completion of embryonic genome activation. EMBO reports. Available at: http://dx.doi.org/10.15252/embr.202153968.
  2. Arand, J., Reijo Pera, R.A. & Wossidlo, M., 2021. Reprogramming of DNA methylation is linked to successful human preimplantation development. Histochemistry and Cell Biology, 156(3), pp.197–207. Available at: http://dx.doi.org/10.1007/s00418-021-02008-6.
  3. Srinivasan, R. et al., 2020. Zscan4 binds nucleosomal microsatellite DNA and protects mouse two-cell embryos from DNA damage. Science Advances, 6(12). Available at: http://dx.doi.org/10.1126/sciadv.aaz9115.
  4. Wossidlo, M. et al., 2011. 5-Hydroxymethylcytosine in the mammalian zygote is linked with epigenetic reprogramming. Nature Communications, 2(1). Available at: http://dx.doi.org/10.1038/ncomms1240.
  5. Wossidlo, M. et al., 2010. Dynamic link of DNA demethylation, DNA strand breaks and repair in mouse zygotes. The EMBO Journal, 29(11), pp.1877–1888. Available at: http://dx.doi.org/10.1038/emboj.2010.80.
 
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