
Structural biology of epigenetic targets
Structural biology of epigenetic targets
Chromatin structure is a major barrier to all nuclear processes and its modulation is essential for correct cell growth. There is now clear evidence that defects in chromatin modulation are responsible for a wide range of diseases, including cancer. Epigenetic modifications have a large impact on chromatin structure, acting in synergy with ATP-dependent remodelers, histone variants and histone chaperones to regulate nuclear mechanisms. By combining state-of-the-art biochemical and crystallographic techniques, we aim to understand chromatin remodeling at the molecular level. Three main targets are the current focus of our research: protein arginine methyltransferases (PRMTs), histone chaperones and histone deacetylases (HDACs). Furthermore, we are also developing structurebased rational approaches to characterize small molecule modulators of the biological activities of our targets since they are frequently involved in human diseases. Our team also participates in collaborative research on several related projects which require our specific expertise. Present collaborations concern the structural studies of complexes of cancer-related targets such as the Translationally Controlled Tumor Protein (TCTP) and the mRNA of human histone H4.
Members
Researchers
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Publications
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2012
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Expression of functional full-length hSRC-1 in eukaryotic cells using modified vaccinia virus Ankara and baculovirus
- Judit Osz
- Karine Pradeau-Aubreton
- Robert Drillien
- Nathalie Troffer-Charlier
- Isabelle Kolb-Cheynel
- Arnaud Poterszman
- Marc Ruff
- Dino Moras
- Natacha Rochel
Analytical Biochemistry ; Volume: 426 ; Page: 106-108
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On the Structure and Function of the Phytoene Desaturase CRTI from Pantoea ananatis, a Membrane-Peripheral and FAD-Dependent Oxidase/Isomerase
- Patrick Schaub
- Qiuju Yu
- Sandra Gemmecker
- Pierre Poussin-Courmontagne
- Justine Mailliot
- Alastair McEwen
- Sandro Ghisla
- Salim Al-Babili
- Jean Cavarelli
- Peter Beyer
PLoS ONE ; Volume: 7 ; Page: e39550
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2010
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Noncanonical Tandem SH2 Enables Interaction of Elongation Factor Spt6 with RNA Polymerase II
- Marie-Laure Diebold
- Erin Loeliger
- Michael Koch
- Fred Winston
- Jean Cavarelli
- Christophe Romier
Journal of Biological Chemistry ; Volume: 285 ; Page: 38389-38398
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The structure of an Iws1/Spt6 complex reveals an interaction domain conserved in TFIIS, Elongin A and Med26
- Marie-Laure Diebold
- Michael Koch
- Erin Loeliger
- Vincent Cura
- Fred Winston
- Jean Cavarelli
- Christophe Romier
EMBO Journal ; Volume: 29 ; Page: 3979-3991
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Structure determination of the minimal complex between Tfb5 and Tfb2, two subunits of the yeast transcription/DNA-repair factor TFIIH: a retrospective study
- Denis Kainov
- Vincent Cura
- Marc Vitorino
- Helène Nierengarten
- Pierre Poussin
- Bruno Kieffer
- Jean Cavarelli
- Arnaud Poterszman
Acta crystallographica Section D : Structural biology [1993-...] ; Volume: 66 ; Page: 745-755
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Crystallization and preliminary crystallographic analysis of eukaryotic transcription and mRNA export factor Iws1 from Encephalitozoon cuniculi
- Michael Koch
- Marie-Laure Diebold
- Jean Cavarelli
- Christophe Romier
Acta Crystallographica Section F: Structural Biology and Crystallization Communications ; Volume: 66 ; Page: 207-210
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2008
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Structural basis for group A trichothiodystrophy.
- Denis E. Kainov
- Marc Vitorino
- Jean Cavarelli
- Arnaud Poterszman
- Jean-Marc Egly
Nature Structural and Molecular Biology ; Volume: 15 ; Page: 980-4
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2007
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Functional insights from structures of coactivator-associated arginine methyltransferase 1 domains.
- Nathalie Troffer-Charlier
- Vincent Cura
- Pierre Hassenboehler
- Dino Moras
- Jean Cavarelli
EMBO Journal ; Volume: 26 ; Page: 4391-401
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Crystal structure, biochemical and genetic characterization of yeast and E. cuniculi TAF(II)5 N-terminal domain: implications for TFIID assembly.
- Christophe Romier
- Nicole James
- Catherine Birck
- Jean Cavarelli
- Christian Vivarès
- Martine A Collart
- Dino Moras
Journal of Molecular Biology ; Volume: 368 ; Page: 1292-306
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Expression, purification, crystallization and preliminary crystallographic study of isolated modules of the mouse coactivator-associated arginine methyltransferase 1.
- Nathalie Troffer-Charlier
- Vincent Cura
- Pierre Hassenboehler
- Dino Moras
- Jean Cavarelli
Acta Crystallograph Sect F Struct Biol Cryst Commun ; Volume: 63 ; Page: 330-3
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