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Center for Computational and Digital Health Innovation

Three Dimensional Genome Organization Regulated by Active Loop Extrusion

We use computer simulations and theoretical modeling to understand how genetic material is packed in our cells.

Lead PI:

  • Michael Rubinstein

Center Researchers:

    Related Publications

    • Theory of chromatin organization maintained by active loop extrusion
    • Activity-driven chromatin organization during interphase: Compaction, segregation, and entanglement suppression

    In the News:

    • How a Protein Complex Helps Organize and Compact DNA

    Funding:

    • NSF

    The Challenge

    How a cell manages to fit approximately two meters of DNA into its nucleus remains a mystery. Additionally, the way that DNA is looped in our cells can influence how frequently different genes are expressed.

    Our goal is to develop a physical understanding of the compact structure of our genome that also helps explain the role of genome organization in gene regulation.

    Our Solution

    We think of our genetic material in the form of chromatin as really long polymers. We apply techniques from polymer physics to model how motor proteins modify chromatin conformations and dynamics through a process known as active loop extrusion and use computer simulations to validate our theories.

    By comparing our predictions to existing experimental data, we can deepen our understanding of the physics of the genome. Hopefully our work can help inform experiments designed to control the organization of specific genomic regions.

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