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Dr Jean Giacomotto
Dr

Jean Giacomotto

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Overview

Background

Dr Giacomotto, NHMRC Emerging Leader, is a young group leader focusing on translational research, genes and diseases, imaging/automatic systems, drug discovery, chemical biology, and medical applications. His work focuses on translating little discoveries made in a single cell or in a model organism to applications or treatments for humans. He has already made discoveries that benefit human health, such as treatment for muscular dystrophies. He is working with a wide diversity of models, including cell lines and mouse models, but he recently spent a lot of time working with the zebrafish model. He believes that this small fish will have an important impact on the seek of treatments for neuromuscular and neurological disorders. Those diseases are very difficult to reproduce in a single cell, making the search for chemical treatments difficult. This fish opens a new avenue for the screening of bioactive compounds and for understanding the progression of these terrible disorders. He believes in translational research, the zebrafish is for him a fantastic complementary model to cell lines in order to recapitulate human diseases and run large-scale experiments. He is working on developing future therapeutical strategies to alleviate the suffering of human patients.

Dr Giacomotto recently established his group at Griffith Research Institute for Drug Discovery (Discovery Biology, Griffith University) and remain an active honorary fellow of the Queensland Brain Institute (The University of Queensland). Dr Giacomotto is currently recruiting. Don't hesitate to contact him for further information.

Dr Giacomotto Laboratory Website

Availability

Dr Jean Giacomotto is:
Available for supervision

Qualifications

  • Doctor of Philosophy, Université Claude Bernard Lyon 1

Research impacts

more to come.

Works

Search Professor Jean Giacomotto’s works on UQ eSpace

33 works between 2006 and 2025

21 - 33 of 33 works

2015

Journal Article

Copy number variants in patients with intellectual disability affect the regulation of ARX transcription factor gene

Ishibashi, Minaka, Manning, Elizabeth, Shoubridge, Cheryl, Krecsmarik, Monika, Hawkins, Thomas A, Giacomotto, Jean, Zhao, Ting, Mueller, Thomas, Bader, Patricia I., Cheung, Sau W., Stankiewicz, Pawel, Bain, Nicole L., Hackett, Anna, Reddy, Chilamakuri C. S., Mechaly, Alejandro S., Peers, Bernard, Wilson, Stephen W., Lenhard, Boris, Bally-Cuif, Laure, Gecz, Jozef, Becker, Thomas S. and Rinkwitz, Silke (2015). Copy number variants in patients with intellectual disability affect the regulation of ARX transcription factor gene. Human Genetics, 134 (11-12), 1163-1182. doi: 10.1007/s00439-015-1594-x

Copy number variants in patients with intellectual disability affect the regulation of ARX transcription factor gene

2015

Journal Article

Comparative Venomics Reveals the Complex Prey Capture Strategy of the Piscivorous Cone Snail Conus catus

Himaya S.W.A., Jin, Ai-Hua, Dutertre, Sebastien, Giacomotto, Jean, Mohialdeen, Hoshyar, Vetter, Irina, Alewood, Paul F. and Lewis, Richard J. (2015). Comparative Venomics Reveals the Complex Prey Capture Strategy of the Piscivorous Cone Snail Conus catus. Journal of Proteome Research, 14 (10), 4372-4381. doi: 10.1021/acs.jproteome.5b00630

Comparative Venomics Reveals the Complex Prey Capture Strategy of the Piscivorous Cone Snail Conus catus

2015

Journal Article

miR-124 Contributes to the functional maturity of microglia

Svahn, Adam J., Giacomotto, Jean, Graeber, Manuel B., Rinkwitz, Silke and Becker, Thomas S. (2015). miR-124 Contributes to the functional maturity of microglia. Developmental Neurobiology, 76 (5), 1-12. doi: 10.1002/dneu.22328

miR-124 Contributes to the functional maturity of microglia

2015

Journal Article

Effective heritable gene knockdown in zebrafish using synthetic microRNAs

Giacomotto, Jean, Rinkwitz, Silke and Becker, Thomas S. (2015). Effective heritable gene knockdown in zebrafish using synthetic microRNAs. Nature Communications, 6 (7378) 7378, 1-11. doi: 10.1038/ncomms8378

Effective heritable gene knockdown in zebrafish using synthetic microRNAs

2015

Journal Article

Motor neuron-expressed microRNAs 218 and their enhancers are nested within introns of Slit2/3 genes

Punnamoottil, Beena, Rinkwitz, Silke, Giacomotto, Jean, Svahn, Adam J. and Becker, Thomas S. (2015). Motor neuron-expressed microRNAs 218 and their enhancers are nested within introns of Slit2/3 genes. Genesis, 53 (5), 321-328. doi: 10.1002/dvg.22852

Motor neuron-expressed microRNAs 218 and their enhancers are nested within introns of Slit2/3 genes

2013

Journal Article

Chemical genetics unveils a key role of mitochondrial dynamics, cytochrome c release and ip3r activity in muscular dystrophy

Giacomotto, Jean, Brouilly, Nicolas, Walter, Ludivine, Mariol, Marie-Christine, Berger, Joachim, Segalat, Laurent, Becker, Thomas S., Currie, Peter D. and Gieseler, Kathrin (2013). Chemical genetics unveils a key role of mitochondrial dynamics, cytochrome c release and ip3r activity in muscular dystrophy. Human Molecular Genetics, 22 (22) ddt302, 4562-4578. doi: 10.1093/hmg/ddt302

Chemical genetics unveils a key role of mitochondrial dynamics, cytochrome c release and ip3r activity in muscular dystrophy

2012

Journal Article

Pax4 is not essential for beta-cell differentiation in zebrafish embryos but modulates alpha-cell generation by repressing arx gene expression

Djiotsa, Joachim, Verbruggen, Vincianne, Giacomotto, Jean, Ishibashi, Minaka, Manning, Elisabeth, Rinkwitz, Silke, Manfroid, Isabelle, Lvoz, Marianne L. and Peers, Bernard (2012). Pax4 is not essential for beta-cell differentiation in zebrafish embryos but modulates alpha-cell generation by repressing arx gene expression. BMC Developmental Biology, 12 (1) 37, 37.1-37.16. doi: 10.1186/1471-213X-12-37

Pax4 is not essential for beta-cell differentiation in zebrafish embryos but modulates alpha-cell generation by repressing arx gene expression

2011

Journal Article

Caenorhabditis elegans as a chemical screening tool for the study of neuromuscular disorders. Manual and semi-automated methods

Giacomotto, Jean, Segalat, Laurent, Carre-Pierrat, Maite and Gieseler, Kathrin (2011). Caenorhabditis elegans as a chemical screening tool for the study of neuromuscular disorders. Manual and semi-automated methods. Methods, 56 (1), 103-113. doi: 10.1016/j.ymeth.2011.10.010

Caenorhabditis elegans as a chemical screening tool for the study of neuromuscular disorders. Manual and semi-automated methods

2010

Journal Article

High-throughput screening and small animal models, where are we?

Giacomotto, Jean and Segalat, Laurent (2010). High-throughput screening and small animal models, where are we?. British Journal of Pharmacology, 160 (2), 204-216. doi: 10.1111/j.1476-5381.2010.00725.x

High-throughput screening and small animal models, where are we?

2009

Journal Article

Metabolic profiling strategy of Caenorhabditis elegans by whole-organism nuclear magnetic resonance

Blaise, Benjamin J., Giacomotto, Jean, Triba, Mohamed N., Toulhoat, Pierre, Piotto, Martial, Emsley, Lyndon, Segalat, Laurent, Dumas, Marc-Emmanuel and Elena, Benedicte (2009). Metabolic profiling strategy of Caenorhabditis elegans by whole-organism nuclear magnetic resonance. Journal of Proteome Research, 8 (5), 2542-2550. doi: 10.1021/pr900012d

Metabolic profiling strategy of Caenorhabditis elegans by whole-organism nuclear magnetic resonance

2009

Journal Article

Evaluation of the therapeutic potential of carbonic anhydrase inhibitors in two animal models of dystrophin deficient muscular dystrophy

Giacomotto, Jean, Pertl, Cordula, Borrel, Caroline, Walter, Maggie C., Bulst, Stefanie, Johnsen, Bob, Baillie, David L., Lochmuller, Hanns, Thirion, Christian and Segalat, Laurent (2009). Evaluation of the therapeutic potential of carbonic anhydrase inhibitors in two animal models of dystrophin deficient muscular dystrophy. Human Molecular Genetics, 18 (21), 4089-4101. doi: 10.1093/hmg/ddp358

Evaluation of the therapeutic potential of carbonic anhydrase inhibitors in two animal models of dystrophin deficient muscular dystrophy

2007

Journal Article

Metabotyping of Caenorhabditis elegans reveals latent phenotypes

Blaise, Benjamin J., Giacomotto, Jean, Elena, Benedicte, Dumas, Marc-Emmanuel, Toulhoat, Pierre, Segalat, Laurent and Emsley, Lyndon (2007). Metabotyping of Caenorhabditis elegans reveals latent phenotypes. Proceedings of the National Academy of Sciences of the United States of America, 104 (50), 19808-19812. doi: 10.1073/pnas.0707393104

Metabotyping of Caenorhabditis elegans reveals latent phenotypes

2006

Journal Article

Blocking of striated muscle degeneration by serotonin in C. elegans

Carre-Pierrat, Maite´, Mariol, Marie-Christine, Chambonnier, Lucie, Laugraud, Aurelie, Heskia, Fabienne, Giacomotto, Jean and Segalat, Laurent (2006). Blocking of striated muscle degeneration by serotonin in C. elegans. Journal of Muscle Research and Cell Motility, 27 (3-4), 253-258. doi: 10.1007/s10974-006-9070-9

Blocking of striated muscle degeneration by serotonin in C. elegans

Funding

Past funding

  • 2020 - 2022
    ZebraClinics. From the identification of drugs against neurodegeneration to a better understanding of synaptic development and function.
    NHMRC Investigator Grants
    Open grant
  • 2019 - 2021
    Unveiling the pathogenic role of the schizophrenia and autism risk-gene NRXN1 in synaptogenesis
    RL Cooper Medical Research Foundation Limited
    Open grant
  • 2019 - 2022
    Investigating the neuro-developmental role of schizophrenia-associated genes using the zebrafish.
    NHMRC Project Grant
    Open grant
  • 2017
    CASS Travel Grant - Innovation genetic approach to recapitulate and study SMA in the zebrafish
    The Cass Foundation Limited
    Open grant
  • 2017 - 2019
    Zebrafish models of Spinal Muscular Atrophy optimized for chemical genetics and drug discovery. From proof-of-principle to new insights and treatments
    Cure SMA
    Open grant
  • 2017 - 2018
    New and innovative polygenic approach for understanding and modelling MNDs in zebrafish
    Motor Neurone Disease Research Institute of Australia Inc
    Open grant
  • 2016 - 2017
    Using the Zebrafish to fight psychiatric disorders. From proof-of-principle to new insights and treatments
    RL Cooper Medical Research Foundation Limited
    Open grant
  • 2015 - 2016
    Investigating drug treatments for a Machado Joseph disease using transgenic zebrafish (NHMRC Project Grant administered by Macquarie University)
    Macquarie University
    Open grant

Supervision

Availability

Dr Jean Giacomotto is:
Available for supervision

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Available projects

  • Unveiling the pathogenicity of genes recently associated with mental disorders

    Our laboratory uses diverse state-of-the-art approaches to try understanding and developing new drugs for mental disorders and Schizophrenia in particular. We start from Genome Wide Association Studies (GWAS) for identifying risk-genes to further study their role in cell lines and animal models. We are currently establishing a pipeline aiming to use the zebrafish animal model to test/observe the neuropathogenicity of the identified gene candidates in regard to brain structure and function. We have position for candidates aiming at learning genome editing techniques such as CRISPR/Cas9 and high-end microscopy. These projects are of high potential and should lead to post-PhD project/appointment and high impact publications. In the long term, this work aims at better understanding the mechanisms involved in the onset, progress and severity of mental disorders. The candidates would benefit from a very highly competitive environment, with international expert and collaborations in the feild.

  • Drug discovery and big pharma partnership to find new neuroactive drugs

    The zebrafish is becoming is prime model for drug discovery. We have been leader in the use of small animal models in drug discovery, and may be some of the very first from identification of a compound in the lab to a drug in clinics. Small animal models such as the zebrafish are compatible with industrial drug discovery techniques such as High Throughput Screening (HTS). We are working at recapitulating human diseases in this organism and try to establish models with early phenotype that can be observed/quantified through automatic readout. We have for instance developed versatile models of neurodegeneration that could help identify/develop drugs against neurodegenerative and motor neuron diseases. We have a set of projects aiming at either i) developing new models that would fit our screening pipeline and/or ii) using the current models to run drug discovery programs and translation (mouse validation via collabs). These projects are strongly bond with the pharma industry and highly collaborative which would be ideal for candidates aiming to join the industry or work in a multidisciplinary environment.

    See attached link for example (https://sites.google.com/view/giacomotto-lab/areas-of-interest?authuser=0)

  • Developing models of motor neuron disease

    Our third research direction aims at developping models of motor neuron degeneration or neurodegeneration per se. This project takes benefit of collaborations of excellence and aims at better understanding the pathogenic mechanisms that could trigger or modulate neurodegeneration. This project is also working synergistically with our drug discovery programs to try finding compounds/drugs able to reduce or stop neurodegenetion. It is noteworthy that this program is bond to laboratories in Europe and North America, garanteeing a highly productive environment, travel opportunuities as well as postdoc options post-PhD. Interestingly, we would have great funding opportunuities for the right candidate and fellowship option post-PhD, which would help tremendously in career development.

    https://sites.google.com/view/giacomotto-lab/home?authuser=0

  • Short term, long term and transgenerational effect of current antipsychotic and antidepressant medications.

    We are looking at studying the short term as well as the long term and transgenerational transcriptomic effect of current antipsychotic and antidepressant medications. This would be done using hte zebrafish animal models.

Supervision history

Completed supervision

Media

Enquiries

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