Author

A. Corpet

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Microbiology· 2 Biochemistry· 1

Signature Assays, Organisms & Methods

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Organism:human· 3 Assay:ChIP-seq· 2 Research Focus:chromatin & epigenetic regulation· 2 Approach:experimental assay· 2 Research Focus:host-pathogen & immune response· 1 Organism:mouse· 1 Assay:proteomics· 1 Approach:statistical model· 1

Frequent Co-Authors

O. Binda· 3 shared P. Lomonte· 3 shared C. Cohen· 2 shared M. Labetoulle· 2 shared P. Texier· 2 shared A. B. Kimenyi Ishimwe· 1 shared A. Fradet-Turcotte· 1 shared A. Rousseau· 1 shared

Activity by Year

2017-2024 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 31 mutual co-author links

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3 shared papersMicrobiology

O. Binda

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Author profile →

3 papers

Recent·Most cited

The HUSH epigenetic repressor complex silences PML nuclear bodies-associated HSV-1 quiescent genomes

S. Roubille, T. Escure, F. Juillard, A. Corpet, R. Neplaz, O. Binda, C. Seurre, M. Gonin, S. Bloor, C. Cohen, P. Texier, O. Haigh, O. Pascual, Y. Ganor, F. Magdinier, , P. Lomonte

This paper identifies the HUSH-SETDB1-MORC2 complex as essential for maintaining HSV-1 latency by promoting H3K9me3 chromatin marks on viral genomes in neurons.

bioRxiv · Jun 18, 2024Microbiology

The TUDOR domain of SMN is an H3K79me1 histone mark reader

O. Binda, A. B. Kimenyi Ishimwe, M. Galloy, K. Jacquet, A. Corpet, A. Fradet-Turcotte, J. Cote, P. Lomonte

This study identifies SMN's TUDOR domain as an H3K79me1 histone mark reader and shows SMA-linked mutations disrupt this interaction.

bioRxiv · Oct 6, 2022Biochemistry

Promyelocytic Leukemia (PML) Nuclear Bodies (NBs) Induce Latent/Quiescent HSV-1 Genomes Chromatinization Through a PML-NB/Histone H3.3/H3.3 Chaperone Axis

C. Cohen, A. Corpet, M. A. Maroui, O. Binda, N. Poccardi, A. Rousseau, P. Texier, N. Sawtell, M. Labetoulle, P. Lomonte

This study shows PML-NBs facilitate HSV-1 latency by promoting H3.3-dependent chromatinization of viral genomes through H3.3 chaperone complexes.

bioRxiv · Nov 9, 2017Microbiology