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13.08.2024 18:02

Mutations in the STAG2 Protein and the Associated Spatial Alteration of DNA Structure Can Cause Leukemia

Dr. Kerstin Wild Stabsstelle „Strategische Entwicklung“
Leibniz-Institut für Immuntherapie

    Researchers at the Leibniz Institute for Immunotherapy (LIT) studied hundreds of patients with acute myeloid leukemia (AML). They discovered that specific mutations in the STAG2 protein cause altered DNA folding in the cell nucleus, thereby contributing to the development of AML.

    Background
    The three-dimensional structure of DNA in the nucleus is stabilized by the cohesin protein complex. It helps to properly fold the DNA and thus regulate gene activity. Cohesin contains two very similar subunits, STAG1 or STAG2. In myeloid leukemias, mutations in the cohesin subunit STAG2 are particularly common, while those in STAG1 are almost never observed. "We wanted to find out why the STAG2 subunit is so often affected and how a mutation leading to the loss of cohesin complex function could contribute to the development of leukemia," explains Prof. Michael Rehli, the head of the LIT research group.

    Study Results
    In collaboration with Prof. Ruud Delwel of the Erasmus Medical Center in Rotterdam, the researchers examined changes in the spatial DNA structure in AML patient samples with and without cohesin mutations. They found that mutations in STAG2 lead to alterations in the DNA structure in AML cells. These changes impair normal gene regulation, resulting in certain genes being either overly activated or not activated at all. What is particularly remarkable about this discovery is that these disturbances cannot be compensated for by the STAG1 protein, highlighting the role of STAG2 in AML.
    In a further step, the researchers examined hematopoietic stem cells from the umbilical cord blood of newborns. These stem cells are precursor cells that can develop into blood and immune cells. "We deactivated STAG2 in these cells, after which they struggled to develop normally and remained in an immature state—a characteristic typical of AML. Interestingly, this problem did not occur when STAG1 was deactivated instead. This shows how important STAG2 is for the normal development of these cells," explains lead author Dr. Alexander Fischer.

    Conclusions
    The results illustrate that STAG2 plays a central role in the organization of DNA, the regulation of gene activity, and the differentiation of hematopoietic stem cells into blood and immune cells. Mutations in the STAG2 gene can therefore lead to the development of AML. "This innovative research provides valuable insights into the molecular mechanisms of AML and could open up new approaches for diagnosis and therapy," summarizes project leader Dr. Claudia Gebhard, emphasizing the significance of the findings.

    About the Leibniz Institute for Immunotherapy (LIT)
    The LIT is an institute within the Leibniz Association located in Regensburg, Germany. Our mission is to develop innovative therapies for the treatment of cancer, autoimmunity, and chronic inflammation. By reprogramming immune cells through synthetic and pharmacological strategies, we build cells that save lives.


    Wissenschaftliche Ansprechpartner:

    Dr. Claudia Gebhard
    NGS Core lab leader and PI
    Telefon: +49 941 944 18186
    Phone: Claudia.Gebhard@lit.eu

    Dr. Alexander Fischer
    Postdoc
    Phone: +49 941 944 38477
    E-Mail: Alexander.Fischer@lit.eu
    LIT- Leibniz Institut für Immuntherapie
    c/o Universitätsklinikum Regensburg
    Franz-Josef-Strauss-Allee 11
    93053 Regensburg


    Originalpublikation:

    Alexander Fischer, Benjamín Hernández-Rodríguez, Roger Mulet-Lazaro, Margit Nuetzel, Fabian Hölzl, Stanley van Herk, François G. Kavelaars, Hanna Stanewsky, Ute Ackermann, Amadou H. Niang, Noelia Diaz, Edith Reuschel, Nicholas Strieder, Inmaculada Hernández-López, Peter J.M. Valk, Juan M. Vaquerizas, Michael Rehli, Ruud Delwel, Claudia Gebhard. STAG2 mutations reshape the cohesin-structured spatial chromatin architecture to drive gene regulation in acute myeloid leukemia. Cell Reports, 2024.

    https://doi.org/10.1016/j.celrep.2024.114498


    Bilder

    AI-generated artistic representation of a mutated cohesin complex
    AI-generated artistic representation of a mutated cohesin complex

    LIT


    Merkmale dieser Pressemitteilung:
    Journalisten, Wissenschaftler
    Biologie, Medizin
    überregional
    Forschungsergebnisse
    Englisch


     

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