
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
Engineers
Publications
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2005
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Inactivation of the peroxisomal ABCD2 transporter in the mouse leads to late-onset ataxia involving mitochondria, Golgi and endoplasmic reticulum damage.
- Isidre Ferrer
- Josef P Kapfhammer
- Colette Hindelang
- Stephan Kemp
- Nathalie Troffer-Charlier
- Vania Broccoli
- Noëlle Callyzot
- Petra Mooyer
- Jacqueline Selhorst
- Peter Vreken
- Ronald J A Wanders
- Jean-Louis Mandel
- Aurora Pujol
Human Molecular Genetics ; Volume: 14 ; Page: 3565-77
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Crystallization and preliminary X-ray crystallographic study of the wild type and two mutants of the CP1 hydrolytic domain from Aquifex aeolicus leucyl-tRNA synthetase.
- Vincent Cura
- Natacha Olieric
- Alexandre Guichard
- En-Duo Wang
- Dino Moras
- Gilbert Eriani
- Jean Cavarelli
Acta crystallographica Section F : Structural biology communications [2014-...] ; Volume: 61 ; Page: 899-901
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Biochemical and NMR mapping of the interface between CREB-binding protein and ligand binding domains of nuclear receptor: beyond the LXXLL motif.
- Fabrice a C Klein
- Robert Andrew Atkinson
- Noelle Potier
- Dino Moras
- Jean Cavarelli
Journal of Biological Chemistry ; Volume: 280 ; Page: 5682-92
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Cloning, purification and crystallization of a Walker-type Pyrococcus abyssi ATPase family member
- Muriel Uhring
- Gilbert Bey
- Odile Lecompte
- Jean Cavarelli
- Dino Moras
- Olivier Poch
Acta Crystallographica Section F: Structural Biology and Crystallization Communications ; Volume: 61 ; Page: 925-927
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2004
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Translationally controlled tumor protein is a target of tumor reversion
- Marcel Tuynder
- Giusy Fiucci
- Sylvie Prieur
- Alexandra Lespagnol
- Anne Géant
- Séverine Beaucourt
- Dominique Duflaut
- Stéphanie Besse
- Laurent Susini
- Jean Cavarelli
- Dino Moras
- Robert Amson
- Adam Telerman
- A. Geant
Proceedings of the National Academy of Sciences of the United States of America ; Volume: 101 ; Page: 15364-15369
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Mutation and evolution of the magnesium-binding site of a class II aminoacyl-tRNA synthetase.
- Laurent Ador
- Sophie Jaeger
- Renaud Geslain
- Franck Martin
- Jean Cavarelli
- Gilbert Eriani
Biochemistry ; Volume: 43 ; Page: 7028-37
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2001
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Crucial Role of the HIGH-loop Lysine for the Catalytic Activity of Arginyl-tRNA Synthetase
- Shun-Ichi Sekine
- Atsushi Shimada
- Osamu Nureki
- Jean Cavarelli
- Dino Moras
- Dmitry G. Vassylyev
- Shigeyuki Yokoyama
Journal of Biological Chemistry ; Volume: 276 ; Page: 3723-3726
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2000
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Crystallization and preliminary X-ray crystallographic analysis of yeast arginyl-tRNA synthetase–yeast tRNAArg complexes
- Bénédicte Delagoutte
- Gérard Keith
- Dino Moras
- Jean Cavarelli
Acta Crystallographica Section D: Biological Crystallography ; Volume: 56 ; Page: 492-494
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In vivo selection of lethal mutations reveals two functional domains in arginyl–tRNA synthetase
- Renaud Geslain
- Franck Martin
- Bénédicte Delagoutte
- Jean Cavarelli
- Jean Gangloff
- Gilbert Eriani
RNA ; Volume: 6 ; Page: 434-448
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1999
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Aminoacyl-tRNA synthetases: a family of expanding functions. Mittelwihr, France, October 10-15, 1999
- Susan A. Martinis
- Pierre Plateau
- Jean Cavarelli
- Catherine Florentz
EMBO Journal ; Volume: 18 ; Page: 4591-4596
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