Benoit Coulombe
}}Benoit Coulombe (born 1958 in Granby, Quebec) is a Canadian scientist whose research focuses on the mechanisms by which regulated protein–protein, protein–DNA and protein–RNA interactions control the activity of RNA polymerase II, the molecular machine that synthesizes all messenger RNA (mRNA) and some small-nuclear RNA (snRNA) in eukaryotes. Coulombe obtained his bachelor's degree in Biochemistry in 1981 and his PhD in Molecular Biology in 1988 at the University of Montreal, before undertaking postdoctoral work at the University of Toronto and the Free University of Brussels. In 1993 he moved to the University of Sherbrooke as an Assistant Professor, later attaining the tenured rank of Full Professor. In 2001 he moved to the Institut de recherches cliniques de Montréal. Coulombe is best known for his "promoter wrapping model" for transcriptional initiation by multi-subunit RNA polymerases, which has been described in molecular biology textbooks. More recently, his laboratory has used protein affinity purification coupled with mass spectrometry to generate high-resolution maps of the interactome of human RNA polymerases. In 2012, the Coulombe laboratory discovered that methylation of molecular chaperones is a central element of a posttranslational modification code, they termed the "chaperone code", that orchestrates the functional organization of the proteome. Provided by Wikipedia
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Discovery of Antivirals Using Phage Display by Esen Sokullu, Marie-Soleil Gauthier, Benoit Coulombe
Published 2021-06-01
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The 37TrillionCells initiative for improving global healthcare via cell-based interception and precision medicine: focus on neurodegenerative diseases by Benoit Coulombe, Thomas M. Durcan, Geneviève Bernard, Asmae Moursli, Christian Poitras, Denis Faubert, Maxime Pinard
Published 2024-04-01
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Biallelic pathogenic variants in POLR3D alter tRNA transcription and cause a hypomyelinating leukodystrophy: A case report by Julia Macintosh, Julia Macintosh, Stefanie Perrier, Stefanie Perrier, Maxime Pinard, Luan T. Tran, Luan T. Tran, Kether Guerrero, Kether Guerrero, Chitra Prasad, Chitra Prasad, Chitra Prasad, Asuri N. Prasad, Asuri N. Prasad, Tomi Pastinen, Tomi Pastinen, Tomi Pastinen, Isabelle Thiffault, Isabelle Thiffault, Isabelle Thiffault, Benoit Coulombe, Benoit Coulombe, Geneviève Bernard, Geneviève Bernard, Geneviève Bernard, Geneviève Bernard, Geneviève Bernard
Published 2023-10-01
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Structural and functional characterization of the IgSF21-neurexin2α complex and its related signaling pathways in the regulation of inhibitory synapse organization by Nicolas Chofflet, Nicolas Chofflet, Yusuke Naito, Yusuke Naito, Anthony John Pastore, Nirmala Padmanabhan, Nirmala Padmanabhan, Phuong Trang Nguyen, Christian Poitras, Benjamin Feller, Benjamin Feller, Nayoung Yi, Nayoung Yi, Jeremie Van Prooijen, Husam Khaled, Husam Khaled, Benoit Coulombe, Benoit Coulombe, Steven J. Clapcote, Steve Bourgault, Tabrez J. Siddiqui, Tabrez J. Siddiqui, Tabrez J. Siddiqui, Tabrez J. Siddiqui, Gabby Rudenko, Hideto Takahashi, Hideto Takahashi, Hideto Takahashi, Hideto Takahashi
Published 2024-03-01
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The leukodystrophy mutation Polr3b R103H causes homozygote mouse embryonic lethality and impairs RNA polymerase III biogenesis by Karine Choquet, Maxime Pinard, Sharon Yang, Robyn D. Moir, Christian Poitras, Marie-Josée Dicaire, Nicolas Sgarioto, Roxanne Larivière, Claudia L. Kleinman, Ian M. Willis, Marie-Soleil Gauthier, Benoit Coulombe, Bernard Brais
Published 2019-06-01
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ARMC5 controls the degradation of most Pol II subunits, and ARMC5 mutation increases neural tube defect risks in mice and humans by Hongyu Luo, Linjiang Lao, Kit Sing Au, Hope Northrup, Xiao He, Diane Forget, Marie-Soleil Gauthier, Benoit Coulombe, Isabelle Bourdeau, Wei Shi, Lucia Gagliardi, Maria Candida Barisson Villares Fragoso, Junzheng Peng, Jiangping Wu
Published 2024-01-01
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Absence of neurological abnormalities in mice homozygous for the Polr3a G672E hypomyelinating leukodystrophy mutation by Karine Choquet, Sharon Yang, Robyn D. Moir, Diane Forget, Roxanne Larivière, Annie Bouchard, Christian Poitras, Nicolas Sgarioto, Marie-Josée Dicaire, Forough Noohi, Timothy E. Kennedy, Joseph Rochford, Geneviève Bernard, Martin Teichmann, Benoit Coulombe, Ian M. Willis, Claudia L. Kleinman, Bernard Brais
Published 2017-04-01
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Whole Exome/Genome Sequencing Joint Analysis of a Family with Oligogenic Familial Hypercholesterolemia by Youmna Ghaleb, Sandy Elbitar, Anne Philippi, Petra El Khoury, Yara Azar, Miangaly Andrianirina, Alexia Loste, Yara Abou-Khalil, Gaël Nicolas, Marie Le Borgne, Philippe Moulin, Mathilde Di-Filippo, Sybil Charrière, Michel Farnier, Cécile Yelnick, Valérie Carreau, Jean Ferrières, Jean-Michel Lecerf, Alexa Derksen, Geneviève Bernard, Marie-Soleil Gauthier, Benoit Coulombe, Dieter Lütjohann, Bertrand Fin, Anne Boland, Robert Olaso, Jean-François Deleuze, Jean-Pierre Rabès, Catherine Boileau, Marianne Abifadel, Mathilde Varret
Published 2022-03-01
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