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.
more to come.
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
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
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
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
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
(2020–2022) NHMRC Investigator Grants
Investigating the neuro-developmental role of schizophrenia-associated genes using the zebrafish.
(2019–2022) NHMRC Project Grant
Unveiling the pathogenic role of the schizophrenia and autism risk-gene NRXN1 in synaptogenesis
(2019–2021) RL Cooper Medical Research Foundation Limited
Dynamic nanoscale organisation of trans-synaptic nanocolumns
Doctor Philosophy
New technologies and models to investigate the functional role of neurexins in zebrafish
(2021) Doctor Philosophy
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
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
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
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
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
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
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. doi: 10.3389/fphys.2023.1221310
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
(2020–2022) NHMRC Investigator Grants
Investigating the neuro-developmental role of schizophrenia-associated genes using the zebrafish.
(2019–2022) NHMRC Project Grant
Unveiling the pathogenic role of the schizophrenia and autism risk-gene NRXN1 in synaptogenesis
(2019–2021) RL Cooper Medical Research Foundation Limited
(2017–2019) Cure SMA
New and innovative polygenic approach for understanding and modelling MNDs in zebrafish
(2017–2018) Motor Neurone Disease Research Institute of Australia Inc
CASS Travel Grant - Innovation genetic approach to recapitulate and study SMA in the zebrafish
(2017) The Cass Foundation Limited
(2016–2017) RL Cooper Medical Research Foundation Limited
(2015–2016) Macquarie University
Dynamic nanoscale organisation of trans-synaptic nanocolumns
Doctor Philosophy — Associate Advisor
Other advisors:
New technologies and models to investigate the functional role of neurexins in zebrafish
(2021) Doctor Philosophy — Associate Advisor
Other advisors:
Note for students: The possible research projects listed on this page may not be comprehensive or up to date. Always feel free to contact the staff for more information, and also with your own research ideas.
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.