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Research Topic : Inheritance
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Epigenetics (incl. Genome Methylation and Epigenomics) (5)
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  • Funded Activity

    Mapping EQTL To Dissect The Genetic Basis Of Complex Trait Variation

    Funder
    National Health and Medical Research Council
    Funding Amount
    $719,525.00
    Summary
    People vary in traits such as height and blood pressure and in their susceptibility to common disease. Part of these differences between individuals is because of their genetic make-up. This research is about understanding which of the genes are involved in common variation and how they work. In particular, the researchers investigate if variation in DNA sequence causes genes to be expressed more or less and how gene expression affects risk of disease.
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    Funded Activity

    Determining The Impact Of Inherited Epigenetic Information On Development And Disease

    Funder
    National Health and Medical Research Council
    Funding Amount
    $511,691.00
    Summary
    Recent observations show that the environment in which you live can alter disease susceptibility in your children, without altering the sequence of your genes. This is due to epigenetic mechanisms which control the way the DNA is interpreted. In this study we will study the potential for epigenetic mechanisms to affect sperm production and impact characteristics and disease in the next generation.
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    Funded Activity

    The Heritability Of Optic Disc Shape

    Funder
    National Health and Medical Research Council
    Funding Amount
    $93,802.00
    Summary
    Evaluation of the optic nerve head (optic disc) is important in the diagnosis of various eye diseases, including glaucoma. The influence of genetics on the shape of the optic disc is not well understood because shape is difficult to measure. Using a novel method of shape analysis, this study will examine optic disc shape in populations of Australian twins and individuals with optic nerve disease. It will contribute to the genetic understanding of the optic nerve head and related disorders.
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    Funded Activity

    Molecular Basis Of Transgenerational Epigenetic Inheritance In Mammals

    Funder
    National Health and Medical Research Council
    Funding Amount
    $477,965.00
    Summary
    While it has long been recognised that it is not just DNA, but chromosomes, that are passed from the gametes to the embryo, the non-DNA component was thought to carry no information with respect to the offspring's ultimate phenotype. However, there is now evidence that the non-DNA component, the epigenetic component, can play a role in the inheritance of phenotype in mammals. This study will attempt to determine the molecular nature of this phenomenon.
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    Funded Activity

    Epilepsy In Twins.

    Funder
    National Health and Medical Research Council
    Funding Amount
    $153,603.00
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    Funded Activity

    Defining The Epigenetic Origins Of Maternally Inherited Disease.

    Funder
    National Health and Medical Research Council
    Funding Amount
    $731,162.00
    Summary
    Epigenetic (non genetic) changes to the DNA in sperm and eggs can alter outcomes in children. Despite the potential for drugs and diet to mediate some of these inherited effects, the processes involved are very poorly understood. By determining the mechanisms that regulate epigenetic inheritance, this project will improve our understanding of how epigenetic mechanisms acting in the parent, can mediate inherited disease and life-long health outcomes in our children.
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    Funded Activity

    Determining The Impacts Of Epigenetic Modifying Drugs On Germline Programming And Offspring Health

    Funder
    National Health and Medical Research Council
    Funding Amount
    $863,918.00
    Summary
    New drugs have been developed that inhibit specific enzymes that regulate epigenetic pathways in cells. These pathways significantly affect growth and development in offspring and may represent a risk to future children of patients taking the drug. This project will determine these risks and provide data for developing clinical guidelines for safe use of the drugs.
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    Funded Activity

    Blood Biomarkers For The Diagnosis Of Pre-clinical Alzheimer’s Disease Employing The Dominantly Inherited Alzheimer Network Cohort

    Funder
    National Health and Medical Research Council
    Funding Amount
    $1,125,804.00
    Summary
    Alzheimer’s disease (AD) is the most common form of dementia and yet a postmortem examination serves as the only definitive diagnosis. The current proposal seeks to investigate alterations in biochemical profiles of individuals who will develop Alzheimer’s disease due to an inherited mutation, against family members who are non-carriers of the mutation, to identify AD related blood changes which can contribute towards the development of a diagnostic blood test for the disease.
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    Funded Activity

    Genetic Basis Of Valvular Heart Disease

    Funder
    National Health and Medical Research Council
    Funding Amount
    $448,771.00
    Summary
    Valvular heart disease is a common cause of heart failure. Identification of the genetic causes of valvular heart disease has important implications in our understanding of these heart diseases, as well as translating these genetic discoveries into better diagnostic and prevention strategies in at-risk families. This research proposal seeks to perform a comprehensive clinical and genetic investigation of individuals and families with the two most common valvular heart diseases, mitral valve prol .... Valvular heart disease is a common cause of heart failure. Identification of the genetic causes of valvular heart disease has important implications in our understanding of these heart diseases, as well as translating these genetic discoveries into better diagnostic and prevention strategies in at-risk families. This research proposal seeks to perform a comprehensive clinical and genetic investigation of individuals and families with the two most common valvular heart diseases, mitral valve prolapse and congenital bicuspid aortic valve.
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    Funded Activity

    Variation And Inheritance Of Retrotransposon Epigenotype In The Mouse

    Funder
    National Health and Medical Research Council
    Funding Amount
    $355,500.00
    Summary
    It is often assumed that traits in humans and other mammals are a product primarily of information encoded in the sequence of DNA, with some contribution from the environment. However, there is clear evidence that traits may vary widely between individuals with precisely the same DNA, such as identical twins, even in circumstances where environmental differences are negligible. This variation can be produced by epigenetic factors chemical changes or protein binding to DNA that alter the way gene .... It is often assumed that traits in humans and other mammals are a product primarily of information encoded in the sequence of DNA, with some contribution from the environment. However, there is clear evidence that traits may vary widely between individuals with precisely the same DNA, such as identical twins, even in circumstances where environmental differences are negligible. This variation can be produced by epigenetic factors chemical changes or protein binding to DNA that alter the way genes are used. Epigenetic factors can be passed from one generation to the next like the DNA itself, and this can make it difficult to know if a trait is encoded in the DNA itself or is epigenetic. We have found that some epigenetic traits in mice are caused by retrotransposons, which are parasitic elements that reside in and among genes, and can reproduce themselves, but do not have any known function (nearly half the human genome is made up of retrotransposons). Retrotransposons are generally kept silent by epigenetic factors, but may sometimes become active; when they do they may disturb normal patterns of gene activity and cause changes in traits and even disease. Much variation in humans may thus be due to variation in the epigenetic state (epigenotype) of retrotransposons. We propose to investigate variation and inheritance of epigenotype in mice, focussing on retrotransposons. We will use simple methods to compare epigenotype of a number of retrotransposons in genetically identical mice, and we will ask if any differences we find are heritable. We will also investigate the resetting of epigenotype the point in development when epigenetic factors are cleared and reset. We suspect that this occurs in early development. These studies may reveal a system of variation and inheritance with rules completely different from those found by Mendel, which may have a pervasive influence on traits, including sporadic diseases in humans.
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