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Current Selection
Status : Active
Scheme : Discovery Projects
Research Topic : DEATH DOMAIN
Australian State/Territory : NSW
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Cell Development, Proliferation and Death (5)
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Cell development proliferation and death (4)
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  • Researchers (39)
  • Funded Activities (9)
  • Organisations (18)
  • Active Funded Activity

    Discovery Projects - Grant ID: DP240101654

    Funder
    Australian Research Council
    Funding Amount
    $732,831.00
    Summary
    Transcriptional and translational regulation of the neuronal protein tau. The microtubule-associated protein tau is important for brain development and performance. To perform these functions, tau levels and its variants are tightly controlled in brain cells. However, the factors that regulate tau remain largely unknown. This project will employ latest gene technologies to identify the molecular regulators of tau, for each step of the process from DNA to the protein. The outcome of this study wi .... Transcriptional and translational regulation of the neuronal protein tau. The microtubule-associated protein tau is important for brain development and performance. To perform these functions, tau levels and its variants are tightly controlled in brain cells. However, the factors that regulate tau remain largely unknown. This project will employ latest gene technologies to identify the molecular regulators of tau, for each step of the process from DNA to the protein. The outcome of this study will significantly advance our understanding of gene regulation and mechanisms for controlling protein levels and contribute to a deeper understanding of brain function during development and aging.
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    Active Funded Activity

    Discovery Projects - Grant ID: DP240101869

    Funder
    Australian Research Council
    Funding Amount
    $703,903.00
    Summary
    Understanding Mitotic Telomere Deprotection. This project aims to study telomeres, the DNA and protein structures that protect chromosome ends. During cell division, cells under stress intentionally uncap their telomeres. This project expects to generate new knowledge that challenges the conventional notion of telomeres as static elements, showing instead that telomeres can be dynamic signalling hubs. Expected outcomes of this project include an understanding of the genetic, proteomic, and signa .... Understanding Mitotic Telomere Deprotection. This project aims to study telomeres, the DNA and protein structures that protect chromosome ends. During cell division, cells under stress intentionally uncap their telomeres. This project expects to generate new knowledge that challenges the conventional notion of telomeres as static elements, showing instead that telomeres can be dynamic signalling hubs. Expected outcomes of this project include an understanding of the genetic, proteomic, and signalling pathways involved in this novel phenomenon. This should provide significant benefits to our fundamental understanding of biological processes that protect human genomes and provide a valuable dataset for research on telomere biology, DNA repair, and genome stability.
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    Active Funded Activity

    Discovery Projects - Grant ID: DP220104036

    Funder
    Australian Research Council
    Funding Amount
    $611,000.00
    Summary
    Mapping networks governing cell state plasticity: how, where and when? Single cell organisms are the basic unit of life, yet, if they had not developed the ability to change cell states we would not exist today. Changing cell states lies at the core of almost every developmental and disease process in multicellular organisms. Building upon our fundamental discovery that stem cells and non-stem cells readily interconvert, we will now incorporate innovative cell systems and the development of our .... Mapping networks governing cell state plasticity: how, where and when? Single cell organisms are the basic unit of life, yet, if they had not developed the ability to change cell states we would not exist today. Changing cell states lies at the core of almost every developmental and disease process in multicellular organisms. Building upon our fundamental discovery that stem cells and non-stem cells readily interconvert, we will now incorporate innovative cell systems and the development of our new multi-layered systems biology strategy to elucidate the first comprehensive understanding of the cell biology that underlies cell state changes. These studies are a major step toward understanding the fundamentals of life.
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    Active Funded Activity

    Discovery Projects - Grant ID: DP210103885

    Funder
    Australian Research Council
    Funding Amount
    $555,892.00
    Summary
    Understanding telomere privilege in pluripotent stem cells. We recently identified that fundamental mechanisms which protect chromosome ends (i.e. “telomeres”) are not conserved between somatic and embryo-derived stem cells. This discovery is without precedent and challenges the dogmatic expectation that cellular functions promoting genome stability are conserved in stem cells. We term the unexpected protective capacity of pluripotent chromosome ends “telomere privilege”. Here we will uncover th .... Understanding telomere privilege in pluripotent stem cells. We recently identified that fundamental mechanisms which protect chromosome ends (i.e. “telomeres”) are not conserved between somatic and embryo-derived stem cells. This discovery is without precedent and challenges the dogmatic expectation that cellular functions promoting genome stability are conserved in stem cells. We term the unexpected protective capacity of pluripotent chromosome ends “telomere privilege”. Here we will uncover the molecular, genomic, and proteomic regulators or telomere privilege; determine the breath of telomere privilege in stem cell lineages; elucidate the functional significance of telomere privilege; and exploit telomere privilege to study fundamental biology related to telomeres and the DNA damage response.
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    Active Funded Activity

    Discovery Projects - Grant ID: DP230102244

    Funder
    Australian Research Council
    Funding Amount
    $422,490.00
    Summary
    Investigating novel pathways in ferroptosis. This project aims to develop new tools to investigate iron-mediated cell death and uncover new pathways involved in ageing. Accumulation of iron leads to frailty in late life, a process that appears common to all animals. Iron becomes reactive and inappropriately triggers a cell death process called ferroptosis leading to dysfunction. To understand these processes and to identify means to intervene, this project aims to use genetic approaches to ident .... Investigating novel pathways in ferroptosis. This project aims to develop new tools to investigate iron-mediated cell death and uncover new pathways involved in ageing. Accumulation of iron leads to frailty in late life, a process that appears common to all animals. Iron becomes reactive and inappropriately triggers a cell death process called ferroptosis leading to dysfunction. To understand these processes and to identify means to intervene, this project aims to use genetic approaches to identify new cell pathways that regulate ferroptosis. This project also aims to develop new tools to study this process. Outcomes of this project may include the identification of potential strategies to alter late life frailty with an expected benefit to life sciences and biotechnology industries.
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    Active Funded Activity

    Discovery Projects - Grant ID: DP200101058

    Funder
    Australian Research Council
    Funding Amount
    $500,000.00
    Summary
    New guardians of the mucosa: Molecular characterisation of M cell biology. We aim to completely define the cellular and molecular biology of gut and lung M cells for the first time. We will elucidate how they develop, are regulated and function at a molecular level, and how M cells maintain normal gut and lung tissues and induce immune responses to protect against microbial challenges. In the future, the new insights will be essential pre-requisites for the development of mucosal-based intervent .... New guardians of the mucosa: Molecular characterisation of M cell biology. We aim to completely define the cellular and molecular biology of gut and lung M cells for the first time. We will elucidate how they develop, are regulated and function at a molecular level, and how M cells maintain normal gut and lung tissues and induce immune responses to protect against microbial challenges. In the future, the new insights will be essential pre-requisites for the development of mucosal-based interventions and vaccines that protect the gut and lung from infectious and inflammatory issues. The harnessing of effective immune responses to control such challenges, are of enormous fundamental and long-standing biological interest, and are amongst the most important areas of current scientific research.
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    Active Funded Activity

    Discovery Projects - Grant ID: DP240100514

    Funder
    Australian Research Council
    Funding Amount
    $1,031,345.00
    Summary
    Chemical staples and chemical probes to dissect dynamins cellular roles. Modulation of protein structure drives cellular function. Dynamin GTPase forms at least two macromolecular structures with different cellular functions. The drivers behind these different structures is unknown. In this project we will leverage our discoveries, and planned enhancements, of chemical biology probes that will modulate dynamin activity by inhibiting at three distinct sites, and one site that stimulates dynamin a .... Chemical staples and chemical probes to dissect dynamins cellular roles. Modulation of protein structure drives cellular function. Dynamin GTPase forms at least two macromolecular structures with different cellular functions. The drivers behind these different structures is unknown. In this project we will leverage our discoveries, and planned enhancements, of chemical biology probes that will modulate dynamin activity by inhibiting at three distinct sites, and one site that stimulates dynamin activity. It is known that Dynamin helices and rings are believed responsible for at least three in cell biological functions: in hormone, neutral and receptor internalisation; cellular mitosis and in actin dynamics. Prior to this work we have lacked the tools to understand the role of shape modulation of protein function.
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    Active Funded Activity

    Discovery Projects - Grant ID: DP200103463

    Funder
    Australian Research Council
    Funding Amount
    $510,000.00
    Summary
    Control of developmental switches by importin 5. Aims: This project will study a key molecular switch called IPO5, a protein that is required for cells and organs to form and function normally, and it will reveal how it works. Significance: These experiments will provide the first complete description of how this molecular switch controls the behaviour of a cell across its lifespan. IPO5 is highly conserved, so these studies will be relevant to a wide range of animals. Expected Outcomes: This k .... Control of developmental switches by importin 5. Aims: This project will study a key molecular switch called IPO5, a protein that is required for cells and organs to form and function normally, and it will reveal how it works. Significance: These experiments will provide the first complete description of how this molecular switch controls the behaviour of a cell across its lifespan. IPO5 is highly conserved, so these studies will be relevant to a wide range of animals. Expected Outcomes: This knowledge will reveal how IPO5 controls formation of sperm by revealing what other proteins it binds to and how this affects cell signaling and responses to the environment. Benefits: This will provide information about potential interventions to control fertility or to repair abnormal cells.
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    Active Funded Activity

    Discovery Projects - Grant ID: DP180101781

    Funder
    Australian Research Council
    Funding Amount
    $802,912.00
    Summary
    Micro-dissection of clathrins role in mitosis via chemical biology probes. This project aims to contribute to understanding the molecular mechanisms of the role of a key protein, clathrin, in cell division. In doing so it expects to reveal new approaches to stop uncontrolled cell division and proliferation, the hallmarks of cancer. The outcomes could in the long term inform breakthroughs in cancer treatment, significant enhancements in life quality and a reduction in cancer death rates.
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    Showing 1-9 of 9 Funded Activites

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