Team
Translational Epigenetics

Dpt: Signaling through Chromatin

Our research activities

Origins and positioning. The team was established in 2012 by Jérôme Govin at the Biosciences and Biotechnology Institute of Grenoble (BIG), with a focus on epigenetic signaling pathways, particularly histone acetylation and bromodomains. Since 2018, the team has been hosted by the Signaling Through Chromatin department of the Institute for Advanced Biosciences (IAB). It now includes a translational research program in onco-hematology, led by Anouk Emadali in close collaboration with clinicians from Grenoble University Hospital (CHU Grenoble Alpes).

Research areas. Our work aims to decipher how epigenetic mechanisms regulate cell fate, both in physiological contexts (gamete differentiation in yeast and mammals) and pathological settings (fungal infections, aggressive B-cell lymphomas). We combine approaches from cell biology, biochemistry, proteomics, structural biology, and bioinformatics to investigate these mechanisms in both fundamental and clinical models.

Translational approach. Our team brings together strong expertise in biology, epigenetic signaling, and clinical research, with seven hospital-affiliated physicians, including Sylvain Carras (Professor of Medicine), who also serves as Deputy Director of both the Clinical Research and Innovation Department (DRCI) and the Biological Resource Center (CRB) at CHU Grenoble. This strong clinical integration, aligned with the CHU’s strategic research priorities (epigenetics, cancer, infertility), allows us to develop high-potential translational projects. We are also engaged at the national level through our participation in the scientific board of the Lymphoma Study Association (LYSA).

A collective dynamics. We actively contribute to the development of the local epigenetics community, especially on the Health Campus. Under the leadership of Jérôme Govin, we implement structuring initiatives such as the Grenoble Epigenetics Club, the Interface Clinics & Epigenetics seminar series, and a strategic partnership between IAB and EMBL.

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Jérôme GOVIN

Team leader

04 76 54 95 84

Our research axes

Our team explores chromatin signaling pathways and how they are deregulated in human diseases. Specifically, we study how chromatin factors control genome organization, gene expression, and cell identity. These mechanisms are largely conserved throughout evolution, from yeast to humans.

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A translational journey in epigenetic and human diseases

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Our major publications

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Humanized Candida and NanoBiT Assays Expedite Discovery of Bdf1 Bromodomain Inhibitors With Antifungal Potential

Wei K. et al.

Advanced Science 2025 The fungal Bromodomain and Extra-Terminal (BET) protein Bdf1 is a potential antifungal target against invasive fungal infections. However, the need to selectively inhibit both Bdf1 bromodomains (BDs) over human orthologs and the lack of molecular tools to

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BET inhibition revealed varying MYC dependency mechanisms independent of gene alterations in aggressive B-cell lymphomas

Delrieu L et al.

Clin Epigenetics 2024 Background: MYC-driven lymphomas are a subset of B-cell lymphomas characterized by genetic alterations that dysregulate the expression of the MYC oncogene. When overexpressed, typically through chromosomal translocations, amplifications, or other mechanis

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Adverse outcome in follicular lymphoma is associated with MYC rearrangements but not MYC extra copies

Bussot L et al.

Br J Haematol 2021

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Extranucleolar CYCLON Staining Pattern Is Strongly Associated to Relapse/Refractory Disease in R-CHOP–treated DLBCL

Bouroumeau A, et al

HemaSphere 2021 Jun 12;5(7):e598

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De novo SMARCA2 variants clustered outside the helicase domain cause a new recognizable syndrome with intellectual disability and blepharophimosis distinct from Nicolaides-Baraitser syndrome

Cappuccio G, et al.

Genet Med . 2020 Nov;22(11):1838-1850. doi: 10.1038/s41436-020-0898-y. Epub 2020 Jul 22.

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Systematic genetic and proteomic screens during gametogenesis identify H2BK34 methylation as an evolutionary conserved meiotic mark

Crespo M, et al.

Epigenetics Chromatin 2020 13(1):35

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A phase 2 study of rituximab, bendamustine, bortezomib and dexamethasone for first-line treatment of older patients with mantle cell lymphoma

Gressin R, et al.

Haematologica 2019 104(1):138-146.

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BET Family Protein BRD4: An Emerging Actor in NFκB Signaling in Inflammation and Cancer

Hajmirza A, et al. 

Biomedicines 2018 6(1)

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Systematic quantitative analysis of H2A and H2B variants by targeted proteomics

El Kennani S, et al. 

Epigenetics Chromatin 2018 11(1):2

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Bdf1 Bromodomains are Essential for Meiosis and the Expression of Meiotic-Specific Genes

García-Oliver E, et al. 

PLoS Genet 2017 13(1):e1006541

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Our activities in pictures

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Our collaborations

  • Carlo Petosa, Institute of Structural Biology (IBS)
  • Charles McKenna, USC Los Angeles, USA
  • Guillermo Orsi, IAB
  • Julien Thévenon, IAB
  • Genaël Rabut, IGDR, Rennes
  • Dominique Helmlinger, CRBM, Montpellier

Our technologies

  • Molecular and cellular biology
  • Cell culture
  • Yeast genetics and biochemistry
  • B cell lymphomas
  • Advances epigenomics (RNA-seq, ChIP-seq, ATAC-seq, Cut&Run-seq, etc)
  • Bioinformatic analysis