Vincent Legagneux
  • E-mail :[email]
  • Phone : 0223234685
  • Location : Rennes, France
Last update 2017-09-11 18:09:38.355

Vincent Legagneux PhD Biological Sciences

Course and current status

Education

  • 1985: Master (ex DEA) in Virology (Université Paris 7 & Institut Pasteur) - Supervisor: Pr. D. Paulin - Title: Expression of Vimentin gene in Burkitt's lymphoma.
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  • 1986-1990: PhD in Biological Sciences (University Paris 7), speciality: Virology - Supervisors: Pr. Michel Morange and Dr. Olivier Bensaude (Institut Pasteur) - Title: Two biochemical studies of the stressed cell in mammals: Increased turnover of HSP90 phosphate groups; Stimulation of two protein-kinases: A RNA Polymerase II CTD-kinase and a kinase related to CDC2.
    Dissertation 3360146 2730572 2806771 2171928 1839451 1936287

 

Post-doctoral Experience

  • 1990-1992: Postdoctoral Researcher - CNRS - Université de Rennes1 (URA256, PI: Dr. H. Beverley Osborne) - Theme: Post-Transcriptional regulations and Development.
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  • 1992-1997: INSERM researcher - CNRS - Université de Rennes1 (URA256, UPR41, PI: Dr. H. Beverley Osborne) - Theme: Post-Transcriptional regulations and Development.
    8114721 8595555 8915529 9427761 10781945 11707455 12799066

  • 1998-2000: INSERM researcher - CNRS - Université de Rennes1 (UPR41, PI: Pr. Katerine Le Guellec) - Theme: Chromosome dynamics in mitosis.
    9852142 12665548 12730203

  • 2000-2004: INSERM researcher - CNRS - Université de Rennes1 (UMR6061, PI: Dr. H. Beverley Osborne) - Theme: Chromosome dynamics in mitosis.
    14516064 14630387 15182703 15632074

  • 2004-2009: INSERM researcher - CNRS - Université de Rennes1 (UMR6026, PI: Pr. Gilles Salbert) - Theme: Spatial organization of the genome and transcriptional control of gene expression.
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  • 2004-2009: INSERM researcher - CNRS - Université de Rennes1 (UMR6061, PI: Dr. H. Beverley Osborne) - Theme: Post-transcriptional control of gene expression.
    19800313 US7863413 US20130004991

  • 2010-2015: INSERM Researcher - CNRS - Université de Rennes 1 - IGDR (UMR6061, UMR6290, PI: Pr. Luc Paillard)- Theme: Post-Transcriptional regulations in Pathology and Development.
    20227387 25512611 26103300 27222809 27546377

  • 2016-: INSERM Researcher - INSERM - Université de Rennes 1 - IRSET (UMR1085, PI: Dr. Nathalie Théret) - Theme: Dynamics of Cellular Microenvironment and Communication.
    hal-01559249

 

Links: ORCID Scholar ResearcherID

 

Research Administration

  • 2004-2007: Elected member of Rennes-1 University scientific board

  • 2004-2008: Elected member of the CNRS scientific section 26 (Development, Evolution, Reproduction, Aging)

  • 2008-2012: Elected member of Rennes-1 University board

  • 2016- : Elected member of INSERM specialized scientific comitee CSS3 (System Physiology and Physiopathology)

Scientific summary

Scientific interests: Gene expression control, Development and homeostasis, Cellular micro-environment.

During the last years, I focused my research on the role of post-transcriptional control of gene expression in embryonic development. I have characterized the role of the RNA-binding protein CELF1 (previously known as EDEN-BP) in regulationg the polyadenylation state, translation and stability of maternal mRNAs in amphibian embryos. More recently, thanks to CELF1_KO mice produced by Luc Paillard, Carole Gautier-Courteille, Chantal Kress and Charles Babinet (17130239), I have deciphered the role of CELF1 in lens homeostasis. I have identified by RNA-seq the CELF1 mRNA targets in lens, and more specifically those regulated at the level of pre-mRNA splicing. This project has given rise to a collaboration with the Salil Lacke's group (University of Delawware)

Beside this, I was involved in a collaborative project with Raphael Métivier on the spatial remodeling of the genome upon transcriptional response to estrogens.

Since january 2016, I joined the team leaded by Nathalie Theret, whose aim is to decipher the role of adamalysins in TGF-β activity in chronic liver diseases (Fibrosis and Cellular Hepatocarcinoma). For this project, we implement complementary approaches such as cell biology, biochemistry, functional genomics, system biology and modeling.

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