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Dr Mel White
Dr

Mel White

Email: 
Phone: 
+61 7 334 62494

Overview

Background

Dr Melanie White heads the Dynamics of Morphogenesis Lab at the Institute for Molecular Bioscience (IMB), University of Queensland and is an ARC Future Fellow. She completed a PhD in Neuroscience at University College London followed by postdoctoral research at The University of Edinburgh. During this time Mel engineered viruses to modulate gene expression in the brain to investigate neuronal function and as a therapeutic approach for neurodegenerative disease. Her work was published in Neuron and PNAS, featured in Nature Reviews Neuroscience and received extensive international media coverage (including the BBC and The Guardian).

In 2012 Mel switched fields to apply quantitative imaging in developmental biology. Her work revealed key mechanisms driving the earliest morphogenetic events in mammalian embryogenesis and was published in Cell, Science, Nature Cell Biology, Developmental Cell and Nature Protocols. Her research was featured on the cover of multiple journals including Cell and she was awarded the inaugural American Society for Cell Biology Porter Prize for Research Excellence (2018).

In 2020, Mel joined the IMB where she will combine her passion for neuroscience and developmental biology to investigate the dynamics of neural tube morphogenesis.

Research overview

The brain and the spinal cord control most of the functions of the body and the mind, yet the dynamics of how they first form is poorly understood. Both structures arise from a common precursor, the neural tube, which forms very early in embryonic development. To generate the forces that sculpt and shape the neural tube, changes in cellular architecture must be tightly coordinated in space and time. These morphological rearrangements occur concurrently with biochemical signalling pathways that specify early neural cell fates.

Our research aims to understand how cellular properties and transcriptional regulators interact with mechanical forces in real time to direct vertebrate neural tube formation and neural cell fate specification. We study the dynamics of neural tube formation by applying advanced imaging technologies in transgenic avian models and human stem cell models.

Availability

Dr Mel White is:
Available for supervision

Qualifications

  • Doctor of Philosophy, University of London

Research impacts

Incorrect formation of the neural tube leads to severe congenital malformations called neural tube defects (NTDs). These are amongst the most common birth defects affecting approximately 300,000 babies worldwide every year. Despite their prevalence, mechanisms causing NTDs in humans remain largely unknown. Our research aims to understand the molecular, cellular and mechanical processes directing neural tube formation. This knowledge is essential for determining the specific causes of NTDs and may provide potential avenues for diagnostic testing and future therapeutic treatments.

Works

Search Professor Mel White’s works on UQ eSpace

32 works between 2003 and 2024

21 - 32 of 32 works

2016

Journal Article

Quantitative imaging of mammalian transcriptional dynamics: from single cells to whole embryos

Zhao, Ziqing W., White, Melanie D., Bissiere, Stephanie, Levi, Valeria and Plachta, Nicolas (2016). Quantitative imaging of mammalian transcriptional dynamics: from single cells to whole embryos. BMC Biology, 14 (1) 115, 115. doi: 10.1186/s12915-016-0331-9

Quantitative imaging of mammalian transcriptional dynamics: from single cells to whole embryos

2016

Book Chapter

Mouse embryo compaction

White, M. D., Bissiere, S., Alvarez, Y. D. and Plachta, N. (2016). Mouse embryo compaction. Mammalian preimplantation development. (pp. 235-58) edited by Melvin L. DePamphilis. Maryland Heights, MO, United States: Academic Press. doi: 10.1016/bs.ctdb.2016.04.005

Mouse embryo compaction

2015

Book Chapter

How adhesion forms the early mammalian embryo

White, Melanie D. and Plachta, Nicolas (2015). How adhesion forms the early mammalian embryo. Cellular adhesion in development and disease. (pp. 1-17) edited by Alpha S. Yap. Maryland Heights, MO, United States: Academic Press. doi: 10.1016/bs.ctdb.2014.11.022

How adhesion forms the early mammalian embryo

2014

Book Chapter

The first cell fate decision during mammalian development

White, Melanie D. and Plachta, Nicolas (2014). The first cell fate decision during mammalian development. Stem Cells, Tissue Engineering and Regenerative Medicine. (pp. 25-40) World Scientific Publishing Co.. doi: 10.1142/9789814612784_0002

The first cell fate decision during mammalian development

2012

Journal Article

Preparation of parasagittal slices for the investigation of dorsal-ventral organization of the rodent medial entorhinal cortex

Pastoll, Hugh, White, Melanie and Nolan, Matthew (2012). Preparation of parasagittal slices for the investigation of dorsal-ventral organization of the rodent medial entorhinal cortex. Journal of Visualized Experiments (61) ARTN e3802. doi: 10.3791/3802

Preparation of parasagittal slices for the investigation of dorsal-ventral organization of the rodent medial entorhinal cortex

2011

Journal Article

A molecular toolbox for rapid generation of viral vectors to up- or down-regulate neuronal gene expression in vivo

White, Melanie D., Milne, Ruth V. J. and Nolan, Matthew F. (2011). A molecular toolbox for rapid generation of viral vectors to up- or down-regulate neuronal gene expression in vivo. Frontiers in Molecular Neuroscience, 4, 1-15. doi: 10.3389/fnmol.2011.00008

A molecular toolbox for rapid generation of viral vectors to up- or down-regulate neuronal gene expression in vivo

2009

Journal Article

RNAi for the treatment of prion disease: a window for intervention in neurodegeneration?

White, Melanie D. and Mallucci, Giovanna R. (2009). RNAi for the treatment of prion disease: a window for intervention in neurodegeneration?. CNS & Neurological Disorders - Drug Targets, 8 (5), 342-352. doi: 10.2174/187152709789541934

RNAi for the treatment of prion disease: a window for intervention in neurodegeneration?

2009

Journal Article

Therapy for prion diseases: insights from the use of RNA interference

White, Melanie D. and Mallucci, Giovanna R. (2009). Therapy for prion diseases: insights from the use of RNA interference. Prion, 3 (3), 121-8. doi: 10.4161/pri.3.3.9289

Therapy for prion diseases: insights from the use of RNA interference

2008

Journal Article

Tuning of synaptic integration in the medial entorhinal cortex to the organization of grid cell firing fields

Garden, Derek L. F., Dodson, Paul D., O'Donnell, Cian, White, Melanie D. and Nolan, Matthew F. (2008). Tuning of synaptic integration in the medial entorhinal cortex to the organization of grid cell firing fields. Neuron, 60 (5), 875-89. doi: 10.1016/j.neuron.2008.10.044

Tuning of synaptic integration in the medial entorhinal cortex to the organization of grid cell firing fields

2008

Journal Article

Single treatment with RNAi against prion protein rescues early neuronal dysfunction and prolongs survival in mice with prion disease

White, Melanie D., Farmer, Michael, Mirabile, Ilaria, Brandner, Sebastian, Collinge, John and Mallucci, Giovanna R. (2008). Single treatment with RNAi against prion protein rescues early neuronal dysfunction and prolongs survival in mice with prion disease. Proceedings of the National Academy of Sciences of the United States of America, 105 (29), 10238-10243. doi: 10.1073/pnas.0802759105

Single treatment with RNAi against prion protein rescues early neuronal dysfunction and prolongs survival in mice with prion disease

2007

Journal Article

Targeting cellular prion protein reverses early cognitive deficits and neurophysiological dysfunction in prion-infected mice

Mallucci, Giovanna R., White, Melanie D., Farmer, Michael, Dickinson, Andrew, Khatun, Husna, Powell, Andrew D., Brandner, Sebastian, Jefferys, John G. R. and Collinge, John (2007). Targeting cellular prion protein reverses early cognitive deficits and neurophysiological dysfunction in prion-infected mice. Neuron, 53 (3), 325-35. doi: 10.1016/j.neuron.2007.01.005

Targeting cellular prion protein reverses early cognitive deficits and neurophysiological dysfunction in prion-infected mice

2003

Journal Article

Positional cloning of a quantitative trait locus on chromosome 13q14 that influences immunoglobulin E levels and asthma

Zhang, Youming, Leaves, Nicholas I, Anderson, Gavin G., Ponting, Chris P., Broxholme, John, Holt, Richard, Edser, Pauline, Bhattacharyya, Sumit, Dunham, Andy, Adcock, Ian M., Pulleyn, Louise, Barnes, Peter J., Harper, John I., Abecasis, Gonçalo, Cardon, Lon, White, Melanie, Burton, John, Matthews, Lucy, Mott, Richard, Ross, Mark, Cox, Roger, Moffatt, Miriam F. and Cookson, William O. C. M. (2003). Positional cloning of a quantitative trait locus on chromosome 13q14 that influences immunoglobulin E levels and asthma. Nature Genetics, 34 (2), 181-6. doi: 10.1038/ng1166

Positional cloning of a quantitative trait locus on chromosome 13q14 that influences immunoglobulin E levels and asthma

Funding

Current funding

  • 2022 - 2025
    Microenvironmental regulation of melanoma brain metastasis
    United States Congressionally Directed Medical Research Programs - Melanoma Research Program
    Open grant
  • 2022 - 2025
    Revealing the mechanobiology of neural tube formation
    ARC Discovery Projects
    Open grant
  • 2022 - 2024
    Revealing how junctional neural tube defects arise
    NHMRC IDEAS Grants
    Open grant
  • 2021 - 2024
    Imaging the foundation of the nervous system
    ARC Future Fellowships
    Open grant

Supervision

Availability

Dr Mel White is:
Available for supervision

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

Available projects

  •  How remodelling of actomyosin networks drives neural tube formation in the living embryo.

    The brain and the spinal cord control most of the functions of the body and the mind, yet the dynamics of how they first form is poorly understood. Both structures arise from a common precursor, the neural tube, which forms very early in embryonic development. Changes in cellular architecture must be tightly coordinated in space and time to generate the forces that sculpt and shape the neural tube. These morphogenetic forces are dependent on the correct regulation of the actin cytoskeleton and many actin-related proteins have been associated with neural tube defects. This PhD project will use quantitative live imaging of developing avian embryos to understand how actin networks are remodelled at the subcellular level to shape the neural tube and which are the key molecules controlling this process.

    Expressions of interest from prospective postgraduate students are welcome. For information on available research higher degree projects, please email melanie.white@imb.uq.edu.au with the following: (1) CV, including a summary of academic qualifications, work and research experience, and publication list; (2) studies report or academic transcript for undergraduate and honours degree(s); and (3) a letter outlining your research interests and career aspirations.

  •  How do tissue-scale forces direct neural tube formation in the living embryo.

    Most tissues and organs are built using a toolbox of common changes in cellular properties such as polarity, adhesion, migration and division, combined with alterations in mechanical forces at the cellular and tissue scales. Not only do cellular properties drive mechanical events within tissues, but mechanical forces also feedback to alter gene expression, signalling pathways and cellular behaviours. These reciprocal interactions are integral to development. This PhD project will utilise high-resolution long-term imaging to link events at the cellular scale to tissue scale forces during neural tube formation in developing avian embryos. Use of tissue tectonics analyses and quantification of cellular behaviours will reveal how different cellular events contribute to morphogenesis of the neural tube. Combining spatiotemporal manipulation of force generation with live cell tracking will demonstrate how the regulation of mechanical forces affects subsequent cell fate and neural tube morphogenesis.

    Expressions of interest from prospective postgraduate students are welcome. For information on available research higher degree projects, please email melanie.white@imb.uq.edu.au with the following: (1) CV, including a summary of academic qualifications, work and research experience, and publication list; (2) studies report or academic transcript for undergraduate and honours degree(s); and (3) a letter outlining your research interests and career aspirations.

Supervision history

Current supervision

  • Doctor Philosophy

    Revealing how the junctional neural tube forms

    Principal Advisor

    Other advisors: Professor Alpha Yap, Dr Yanina Alvarez

  • Doctor Philosophy

    How the interaction between blood flow forces and ECM controls vessel assembly and function during development

    Principal Advisor

    Other advisors: Dr Anne Lagendijk

  • Doctor Philosophy

    Revealing the mechanobiology of neural tube formation

    Principal Advisor

    Other advisors: Professor Robert Parton, Dr Yanina Alvarez

  • Doctor Philosophy

    Understanding Cytoskeletal-Golgi cross talk in cellular pathfinding in crowded tissue environments

    Associate Advisor

    Other advisors: Professor Robert Parton, Dr Samantha Stehbens

  • Doctor Philosophy

    THE ROLE OF EXTRACELLULAR MATRIX AND FOCAL ADHESION DYNAMICS IN STEM CELL COMMITMENT

    Associate Advisor

    Other advisors: Professor Alan Rowan

Media

Enquiries

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

communications@uq.edu.au