Skip to menu Skip to content Skip to footer
Dr Jean Giacomotto
Dr

Jean Giacomotto

Email: 

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

1 - 20 of 33 works

2025

Journal Article

Cre-Lox miRNA-delivery technology optimized for inducible microRNA and gene-silencing studies in zebrafish

Guo, Fangfei, Tromp, Alisha, Wang, Haitao, Hall, Thomas E and Giacomotto, Jean (2025). Cre-Lox miRNA-delivery technology optimized for inducible microRNA and gene-silencing studies in zebrafish. Nucleic Acids Research, 53 (2) gkaf004, 2. doi: 10.1093/nar/gkaf004

Cre-Lox miRNA-delivery technology optimized for inducible microRNA and gene-silencing studies in zebrafish

2024

Journal Article

Clinical and molecular spectrum of autosomal recessive CA8‐related cerebellar ataxia

Kaiyrzhanov, Rauan, Ortigoza‐Escobar, Juan Darío, Stringer, Brett W., Ganieva, Manizha, Gowda, Vykuntaraju K., Srinivasan, Varunvenkat M., Macaya, Alfons, Laner, Andreas, Onbool, Enas, Al‐Shammari, Randa, Al‐Owain, Mohammed, Deconinck, Nicolas, Vilain, Catheline, Dontaine, Pauline, Self, Eleanor, Akram, Rabia, Hussain, Ghulam, Baig, Shahid Mahmood, Iqbal, Javed, Salpietro, Vincenzo, Neshatdoust, Maedeh, Kasiri, Mahboubeh, Yesil, Gozde, Uygur, Turkan, Pysden, Karen, Berry, Ian R., Alves, Cesar Augusto, Giacomotto, Jean, Houlden, Henry and Maroofian, Reza (2024). Clinical and molecular spectrum of autosomal recessive CA8‐related cerebellar ataxia. Movement Disorders, 39 (6), 983-995. doi: 10.1002/mds.29754

Clinical and molecular spectrum of autosomal recessive CA8‐related cerebellar ataxia

2023

Journal Article

Cell surface plasticity in response to shape change in the whole organism

Hall, Thomas E., Ariotti, Nicholas, Lo, Harriet P., Rae, James, Ferguson, Charles, Martel, Nick, Lim, Ye-Wheen, Giacomotto, Jean and Parton, Robert G. (2023). Cell surface plasticity in response to shape change in the whole organism. Current Biology, 33 (19), 4276-4284. doi: 10.1016/j.cub.2023.08.068

Cell surface plasticity in response to shape change in the whole organism

2023

Journal Article

Optimising the zebrafish Cre/Lox toolbox. Codon improved iCre, new gateway tools, Cre protein and guidelines

Tromp, Alisha, Wang, Haitao, Hall, Thomas E., Mowry, Bryan and Giacomotto, Jean (2023). Optimising the zebrafish Cre/Lox toolbox. Codon improved iCre, new gateway tools, Cre protein and guidelines. Frontiers in Physiology, 14 1221310, 1-10. doi: 10.3389/fphys.2023.1221310

Optimising the zebrafish Cre/Lox toolbox. Codon improved iCre, new gateway tools, Cre protein and guidelines

2022

Journal Article

Brain-wide visual habituation networks in wild type and fmr1 zebrafish

Marquez-Legorreta, Emmanuel, Constantin, Lena, Piber, Marielle, Favre-Bulle, Itia A., Taylor, Michael A., Blevins, Ann S., Giacomotto, Jean, Bassett, Dani S., Vanwalleghem, Gilles C. and Scott, Ethan K. (2022). Brain-wide visual habituation networks in wild type and fmr1 zebrafish. Nature Communications, 13 (1) 895. doi: 10.1038/s41467-022-28299-4

Brain-wide visual habituation networks in wild type and fmr1 zebrafish

2022

Journal Article

Functional characterisation of the amyotrophic lateral sclerosis risk locus GPX3/TNIP1

Restuadi, Restuadi, Steyn, Frederik J., Kabashi, Edor, Ngo, Shyuan T., Cheng, Fei-Fei, Nabais, Marta F., Thompson, Mike J., Qi, Ting, Wu, Yang, Henders, Anjali K., Wallace, Leanne, Bye, Chris R., Turner, Bradley J., Ziser, Laura, Mathers, Susan, McCombe, Pamela A., Needham, Merrilee, Schultz, David, Kiernan, Matthew C., van Rheenen, Wouter, van den Berg, Leonard H., Veldink, Jan H., Ophoff, Roel, Gusev, Alexander, Zaitlen, Noah, McRae, Allan F., Henderson, Robert D., Wray, Naomi R., Giacomotto, Jean and Garton, Fleur C. (2022). Functional characterisation of the amyotrophic lateral sclerosis risk locus GPX3/TNIP1. Genome Medicine, 14 (1) 7, 7. doi: 10.1186/s13073-021-01006-6

Functional characterisation of the amyotrophic lateral sclerosis risk locus GPX3/TNIP1

2021

Journal Article

Cavin4 interacts with Bin1 to promote T-tubule formation and stability in developing skeletal muscle

Lo, Harriet P., Lim, Ye-Wheen, Xiong, Zherui, Martel, Nick, Ferguson, Charles, Ariotti, Nicholas, Giacomotto, Jean, Rae, James, Floetenmeyer, Matthias, Moradi, Shayli Varasteh, Gao, Ya, Tillu, Vikas A., Xia, Di, Wang, Huang, Rahnama, Samira, Nixon, Susan J., Bastiani, Michele, Day, Ryan D., Smith, Kelly A., Palpant, Nathan J., Johnston, Wayne A., Alexandrov, Kirill, Collins, Brett M., Hall, Thomas E. and Parton, Robert G. (2021). Cavin4 interacts with Bin1 to promote T-tubule formation and stability in developing skeletal muscle. Journal of Cell Biology, 220 (12) e201905065. doi: 10.1083/jcb.201905065

Cavin4 interacts with Bin1 to promote T-tubule formation and stability in developing skeletal muscle

2021

Journal Article

Pipeline for generating stable large genomic deletions in zebrafish, from small domains to whole gene excisions

Tromp, Alisha, Robinson, Kate, Hall, Thomas E., Mowry, Bryan and Giacomotto, Jean (2021). Pipeline for generating stable large genomic deletions in zebrafish, from small domains to whole gene excisions. G3 Genes|Genomes|Genetics, 11 (12) jkab321. doi: 10.1093/g3journal/jkab321

Pipeline for generating stable large genomic deletions in zebrafish, from small domains to whole gene excisions

2021

Journal Article

Reduced C9orf72 function leads to defective synaptic vesicle release and neuromuscular dysfunction in zebrafish

Butti, Zoé, Pan, Yingzhou Edward, Giacomotto, Jean and Patten, Shunmoogum A. (2021). Reduced C9orf72 function leads to defective synaptic vesicle release and neuromuscular dysfunction in zebrafish. Communications Biology, 4 (1) 792, 1-16. doi: 10.1038/s42003-021-02302-y

Reduced C9orf72 function leads to defective synaptic vesicle release and neuromuscular dysfunction in zebrafish

2020

Journal Article

Modular transient nanoclustering of activated β2-adrenergic receptors revealed by single-molecule tracking of conformation-specific nanobodies

Gormal, Rachel S., Padmanabhan, Pranesh, Kasula, Ravikiran, Bademosi, Adekunle T., Coakley, Sean, Giacomotto, Jean, Blum, Ailisa, Joensuu, Merja, Wallis, Tristan P., Lo, Harriet P., Budnar, Srikanth, Rae, James, Ferguson, Charles, Bastiani, Michele, Thomas, Walter G., Pardon, Els, Steyaert, Jan, Yap, Alpha S., Goodhill, Geoffrey J., Hilliard, Massimo A., Parton, Robert G. and Meunier, Frédéric A. (2020). Modular transient nanoclustering of activated β2-adrenergic receptors revealed by single-molecule tracking of conformation-specific nanobodies. Proceedings of the National Academy of Sciences of the United States of America, 117 (48), 30476-30487. doi: 10.1073/pnas.2007443117

Modular transient nanoclustering of activated β2-adrenergic receptors revealed by single-molecule tracking of conformation-specific nanobodies

2020

Journal Article

Neurexins in autism and schizophrenia-a review of patient mutations, mouse models and potential future directions

Tromp, Alisha, Mowry, Bryan and Giacomotto, Jean (2020). Neurexins in autism and schizophrenia-a review of patient mutations, mouse models and potential future directions. Molecular Psychiatry, 26 (3), 747-760. doi: 10.1038/s41380-020-00944-8

Neurexins in autism and schizophrenia-a review of patient mutations, mouse models and potential future directions

2020

Journal Article

Characterisation of δ-Conotoxin TxVIA as a mammalian T-type calcium channel modulator

Wang, Dan, Himaya, S.W.A., Giacomotto, Jean, Hasan, Md. Mahadhi, Cardoso, Fernanda C., Ragnarsson, Lotten and Lewis, Richard J. (2020). Characterisation of δ-Conotoxin TxVIA as a mammalian T-type calcium channel modulator. Marine Drugs, 18 (7) 343, 1-13. doi: 10.3390/md18070343

Characterisation of δ-Conotoxin TxVIA as a mammalian T-type calcium channel modulator

2020

Conference Publication

Re-evaluating the nirvana cabal deployed by piscivorous cone snails

Dutt, Mriga, Giacomotto, Jean, Ragnarsson, Lotten, Andersson, Asa, Brust, Andreas, Deakan, Zoltan, Alewood, Paul F. and Lewis, Richard J. (2020). Re-evaluating the nirvana cabal deployed by piscivorous cone snails. 20th World Congress of the International Society on Toxinology, Buenos Aires, Argentina, 8-13 September 2019. Oxford, United Kingdom: Elsevier. doi: 10.1016/j.toxicon.2019.10.044

Re-evaluating the nirvana cabal deployed by piscivorous cone snails

2019

Journal Article

The α1-adrenoceptor inhibitor ρ-TIA facilitates net hunting in piscivorous Conus tulipa

Dutt, Mriga, Giacomotto, Jean, Ragnarsson, Lotten, Andersson, Åsa, Brust, Andreas, Dekan, Zoltan, Alewood, Paul F. and Lewis, Richard J. (2019). The α1-adrenoceptor inhibitor ρ-TIA facilitates net hunting in piscivorous Conus tulipa. Scientific Reports, 9 (1) 17841, 17841. doi: 10.1038/s41598-019-54186-y

The α1-adrenoceptor inhibitor ρ-TIA facilitates net hunting in piscivorous Conus tulipa

2019

Journal Article

Association of schizophrenia risk with disordered niacin metabolism in an Indian genome-wide association study

Periyasamy, Sathish, John, Sujit, Padmavati, Raman, Rajendren, Preeti, Thirunavukkarasu, Priyadarshini, Gratten, Jacob, Vinkhuyzen, Anna, McRae, Allan, Holliday, Elizabeth G., Nyholt, Dale R., Nancarrow, Derek, Bakshi, Andrew, Hemani, Gibran, Nertney, Deborah, Smith, Heather, Filippich, Cheryl, Patel, Kalpana, Fowdar, Javed, McLean, Duncan, Tirupati, Srinivasan, Nagasundaram, Arunkumar, Gundugurti, Prasad Rao, Selvaraj, Krishnamurthy, Jegadeesan, Jayaprakash, Jorde, Lynn B., Wray, Naomi R., Brown, Matthew A., Suetani, Rachel, Giacomotto, Jean ... Mowry, Bryan J. (2019). Association of schizophrenia risk with disordered niacin metabolism in an Indian genome-wide association study. JAMA Psychiatry, 76 (10), 1026-1034. doi: 10.1001/jamapsychiatry.2019.1335

Association of schizophrenia risk with disordered niacin metabolism in an Indian genome-wide association study

2019

Conference Publication

Characterization of δ-conotoxin Tx-VIA as selective T-type modulator

Wang, Dan, Himaya, S. W. A., Giacomotto, Jean, Hasan, Mahadhi, Cardoso, Fernanda C. and Lewis, Richard J. (2019). Characterization of δ-conotoxin Tx-VIA as selective T-type modulator. Brisbane Pain Research Symposium: Multidisciplinary Perspectives & Therapeutics 2019, Brisbane, QLD, Australia, 29 November 2019.

Characterization of δ-conotoxin Tx-VIA as selective T-type modulator

2019

Conference Publication

First genome-wide association study of schizophrenia in an Indian population reveals a novel susceptibility locus

Periyasamy, Sathish, John, Sujit, Padmavati, Raman, Rajendren, Preeti, Thirunavukkarasu, Priyadarshini, Gratten, Jacob, Holliday, Elizabeth, Bakshi, Andrew, Jorde, Lynn, Brown, Matthew, Wray, Naomi, Suetani, Rachel, Giacomotto, Jean, Thara, Rangaswamy and Mowry, Bryan (2019). First genome-wide association study of schizophrenia in an Indian population reveals a novel susceptibility locus. 26th World Congress of Psychiatric Genetics (WCPG), Glasgow, Scotland, 11-15 October 2018. Amsterdam, The Netherlands: Elsevier . doi: 10.1016/j.euroneuro.2018.08.017

First genome-wide association study of schizophrenia in an Indian population reveals a novel susceptibility locus

2017

Journal Article

Caveolae protect notochord cells against catastrophic mechanical failure during development

Lim, Ye-Wheen, Lo, Harriet P., Ferguson, Charles, Martel, Nick, Giacomotto, Jean, Gomez, Guillermo A., Yap, Alpha S., Hall, Thomas E. and Parton, Robert G. (2017). Caveolae protect notochord cells against catastrophic mechanical failure during development. Current Biology, 27 (13), 1968-1981.e7. doi: 10.1016/j.cub.2017.05.067

Caveolae protect notochord cells against catastrophic mechanical failure during development

2016

Journal Article

Developmental suppression of schizophrenia-associated miR-137 alters sensorimotor function in zebrafish

Giacomotto, J., Carroll, A. P., Rinkwitz, S., Mowry, B., Cairns, M. J. and Becker, T. S. (2016). Developmental suppression of schizophrenia-associated miR-137 alters sensorimotor function in zebrafish. Translational Psychiatry, 6 (5) e818, 1-10. doi: 10.1038/tp.2016.88

Developmental suppression of schizophrenia-associated miR-137 alters sensorimotor function in zebrafish

2016

Journal Article

Tissue-specific models of spinal muscular atrophy confirm a critical role of SMN in motor neurons from embryonic to adult stages

Laird, Angela S., Mackovski, Nikolce, Rinkwitz, Silke, Becker, Thomas S. and Giacomotto, Jean (2016). Tissue-specific models of spinal muscular atrophy confirm a critical role of SMN in motor neurons from embryonic to adult stages. Human Molecular Genetics, 25 (9) ddw044, 1728-1738. doi: 10.1093/hmg/ddw044

Tissue-specific models of spinal muscular atrophy confirm a critical role of SMN in motor neurons from embryonic to adult stages

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

Before you email them, read our advice on how to contact a supervisor.

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

For media enquiries about Dr Jean Giacomotto's areas of expertise, story ideas and help finding experts, contact our Media team:

communications@uq.edu.au