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Cabianca_Celegans_Larvae1
Helmholtz Munich | Daphne Cabianca

Environment and Nuclear Organization

Cabianca Lab

About our Research

All organisms are constantly exposed to a changing environment, including temperature shifts, a variable availability of nutrients and the presence of pathogens.

Epigenetic modifications link the environment to genome regulation. Therefore, deciphering how the epigenome functionally responds to environmental perturbations is a fundamental question with the potential to shed light on diseases with a strong environmental contribution.

In our group, we aim to understand how environmental inputs modulate the state, spatial organization and function of chromatin, using the roundworm C. elegans as a model system.

We combine a series of cutting-edge techniques that allow us to address our questions from different angles. Among others we utilize:

  • Spinning disc confocal live microscopy to monitor protein and chromatin localization at the subnuclear scale
  • RNAi screens
  • Genetic editing via CRISPR-Cas9 and other methods
  • ChIP, DamID and ATACseq to probe for chromatin state and compartmentalization
  • RNAseq for gene expression
  • Organismal assays like stress survival

Multiple layers of regulation are required to establish and maintain appropriate gene expression patterns. These include chromatin modifications and higher order architecture of the genome.

From yeast to man, the spatial distribution of chromatin is not random and reflects its functional state: in most cells, transcriptionally silenced heterochromatin is actively sequestered at the nuclear and nucleolar periphery while active chromatin is centrally located. The establishment and definition of such spatial genomic architecture occurs during cell differentiation under developmental cues. But what happens to the large-scale 3D chromatin architecture under environmental stimuli? And is there a function for the spatial segregation of euchromatin and heterochromatin in the transcriptional response to unscheduled environmental stresses?

Our current work focuses on the role of nutrients and heat in modulating chromatin organization and tests its role as epigenetic effector of “stress memory,” a phenomenon that allows organisms to better respond to a second stress exposure later in life.

Enzymes that modify chromatin do so using metabolic intermediates as cofactors, therefore the nutritional state of an organism has the potential to directly impact the epigenome of its cells.

Which metabolites and dietary components influence chromatin function? What are the consequences of perturbing them for a developing organism?

In our group, we take advantage of the highly controllable/manipulatable diet and microbiota of C. elegans, to systematically screen for the metabolic requirements of heterochromatin silencing. Using a microscopy-based readout for heterochromatin state combined to genetic screens and microbiota strains we aim to i) identify metabolic enzymes, metabolites, and microbiota components that influence heterochromatin regulation in a multicellular organism and ii) characterize the consequences of their perturbations at the levels of chromatin organization, transcriptional output, and organismal health.

Within the nucleus, euchromatin (active) and heterochromatin (repressed) are spatially separated, with heterochromatin sequestered at the nuclear periphery. In several species, the heterochromatic mark H3K9 methylation is overall the main determinant for anchoring at the nuclear periphery. Nonetheless, H3K9me-independent pathways do exist. Surprisingly, we identified the euchromatic reader MRG-1 as required for the accurate sequestration of heterochromatin in the intestine of C. elegans (Cabianca et al., Nature 2019). In absence of MRG-1, heterochromatin detaches from the nuclear periphery and fails to remain silent, leading to a global perturbation of genome organization and function.

How does the euchromatin reader MRG-1 regulate heterochromatin spatial distribution? MRG-1 is part of multiple protein complexes, which one is responsible to preserve an accurate 3D chromatin organization?

Utilizing a combination of tissue-specific proteomics and genetic tools we aim to unravel the mechanism through which MRG-1 regulates genome architecture and transcription in intestine. Since MRG-1 is highly conserved in multicellular organisms, our work can shed light on conserved mechanisms governing chromatin architecture, potentially uncovering epigenetic contributors to cell identity and tissue homeostasis.

Multiple layers of regulation are required to establish and maintain appropriate gene expression patterns. These include chromatin modifications and higher order architecture of the genome.

From yeast to man, the spatial distribution of chromatin is not random and reflects its functional state: in most cells, transcriptionally silenced heterochromatin is actively sequestered at the nuclear and nucleolar periphery while active chromatin is centrally located. The establishment and definition of such spatial genomic architecture occurs during cell differentiation under developmental cues. But what happens to the large-scale 3D chromatin architecture under environmental stimuli? And is there a function for the spatial segregation of euchromatin and heterochromatin in the transcriptional response to unscheduled environmental stresses?

Our current work focuses on the role of nutrients and heat in modulating chromatin organization and tests its role as epigenetic effector of “stress memory,” a phenomenon that allows organisms to better respond to a second stress exposure later in life.

Enzymes that modify chromatin do so using metabolic intermediates as cofactors, therefore the nutritional state of an organism has the potential to directly impact the epigenome of its cells.

Which metabolites and dietary components influence chromatin function? What are the consequences of perturbing them for a developing organism?

In our group, we take advantage of the highly controllable/manipulatable diet and microbiota of C. elegans, to systematically screen for the metabolic requirements of heterochromatin silencing. Using a microscopy-based readout for heterochromatin state combined to genetic screens and microbiota strains we aim to i) identify metabolic enzymes, metabolites, and microbiota components that influence heterochromatin regulation in a multicellular organism and ii) characterize the consequences of their perturbations at the levels of chromatin organization, transcriptional output, and organismal health.

Within the nucleus, euchromatin (active) and heterochromatin (repressed) are spatially separated, with heterochromatin sequestered at the nuclear periphery. In several species, the heterochromatic mark H3K9 methylation is overall the main determinant for anchoring at the nuclear periphery. Nonetheless, H3K9me-independent pathways do exist. Surprisingly, we identified the euchromatic reader MRG-1 as required for the accurate sequestration of heterochromatin in the intestine of C. elegans (Cabianca et al., Nature 2019). In absence of MRG-1, heterochromatin detaches from the nuclear periphery and fails to remain silent, leading to a global perturbation of genome organization and function.

How does the euchromatin reader MRG-1 regulate heterochromatin spatial distribution? MRG-1 is part of multiple protein complexes, which one is responsible to preserve an accurate 3D chromatin organization?

Utilizing a combination of tissue-specific proteomics and genetic tools we aim to unravel the mechanism through which MRG-1 regulates genome architecture and transcription in intestine. Since MRG-1 is highly conserved in multicellular organisms, our work can shed light on conserved mechanisms governing chromatin architecture, potentially uncovering epigenetic contributors to cell identity and tissue homeostasis.

The Cabianca Lab

Portrait Iratxe Estivariz

Dr. Iratxe Estivariz

Postdoc

Fernanda Plabst Images

Fernanda Pabst

Doctoral Researcher

Nada Saad Norildin Al-Refaie

Doctoral Researcher

Carole.png

Carole Zaratiegui

Doctoral Researcher

Yuri_DAlessio

Yuri D'Alessio

Doctoral Researcher

    Lorenz Pudelko

    Lorenz Pudelko

    Doctoral Researcher

    Johanna Hornung

    Johanna Hornung

    Research Technician

    Portrait Thomas Gerling

    Thomas Gerling

    Administrative Assistant

    After several years of working in procurement, customer support and as an administrative assistant, Thomas started a new career as a team assistant to the IRM-MED at Helmholtz Munich in 2019. Since February 2020 he is assisting at the IFE, and since October 2023 at the IES.

    Latest Lab Publications

    Weiterlesen

    Daphne Cabianca Previous Publications

    1. Cabianca DS, Muñoz-Jiménez C, Kalck V, Gaidatzis D, Padeken J, Seeber A, Askjaer P, Gasser SM. Active chromatin marks drive spatial sequestration of heterochromatin in C. elegans nuclei. Nature. 2019.
    2. Cabianca DS, Gasser SM. Spatial segregation of heterochromatin: Uncovering functionality in a multicellular organism. Nucleus. 2016.
    3. Gonzalez-Sandoval A, Towbin BD, Kalck V, Cabianca DS, Gaidatzis D, Hauer MH, Geng L, Wang L, Yang T, Wang X, Zhao K, Gasser SM. Perinuclear Anchoring of H3K9-Methylated Chromatin Stabilizes Induced Cell Fate in C.  elegans Embryos. Cell. 2015.
    4. Mattout A, Cabianca DS, Gasser SM. Chromatin states and nuclear organization in development--a view from the nuclear lamina. Genome Biol. 2015.
    5. Bonomi S, di Matteo A, Buratti E, Cabianca DS, Baralle FE, Ghigna C, Biamonti G. HnRNP A1 controls a splicing regulatory circuit promoting mesenchymal-to-epithelial transition. Nucleic Acids Res. 2013.
    6. Cabianca DS, Casa V, Gabellini D. A novel molecular mechanism in human genetic disease: a DNA repeat-derived lncRNA. RNA Biol. 2012.
    7. Cabianca DS, Casa V, Bodega B, Xynos A, Ginelli E, Tanaka Y, Gabellini D. A long ncRNA links copy number variation to a polycomb/trithorax epigenetic switch in FSHD muscular dystrophy. Cell. 2012.
    8. Cabianca DS, Gabellini D. The cell biology of disease: FSHD: copy number variations on the theme of muscular dystrophy. J Cell Biol. 2010.

    Contact

    Portrait Thomas Gerling

    Thomas Gerling

    Administrative Assistant