Discovering genes which modify human physical performance: a means of developing healthier life styles & novel athletic training programs. The aim of this multicentred study (University of Sydney, Australian National University, Australian Institute of Sport) is to find genes in the cardiac and musculoskeletal systems that are involved in modifying human physical performance. From this knowledge, it is proposed to develop novel physical training programs in our national sporting institutions ba ....Discovering genes which modify human physical performance: a means of developing healthier life styles & novel athletic training programs. The aim of this multicentred study (University of Sydney, Australian National University, Australian Institute of Sport) is to find genes in the cardiac and musculoskeletal systems that are involved in modifying human physical performance. From this knowledge, it is proposed to develop novel physical training programs in our national sporting institutions based on an individual's genetic information. In the broader community, knowledge of genes which contribute to the normal and healthy functioning of the cardiac and musculoskeletal systems will be invaluable in understanding and preventing breakdowns in these body systems.Read moreRead less
Genetic variation of transcriptional control. Genetic variation is a key cause phenotype differences in humans, animals, and plants and so of great economic importance. Despite its proven importance to human diseases, ?quantitative? variation in the amount of gene expression rather than ?qualitative? protein sequence changes, has not been systematically studied. We have developed a powerful method to identify genetic causes of quantitative variation using crosses of inbred mice in conjunction wi ....Genetic variation of transcriptional control. Genetic variation is a key cause phenotype differences in humans, animals, and plants and so of great economic importance. Despite its proven importance to human diseases, ?quantitative? variation in the amount of gene expression rather than ?qualitative? protein sequence changes, has not been systematically studied. We have developed a powerful method to identify genetic causes of quantitative variation using crosses of inbred mice in conjunction with microarray techniques to analyse expression of thousands of genes simultaneously. These studies will be extended to humans and be significant to wide areas of biological and commercial activity.Read moreRead less
Evolutionary biomedicine: genetic pathologies as selection agents in three model systems. Our environment is changing at a rate never seen before, rendering organisms 'maladapted' if they cannot evolve quickly enough - that is, there will be a mismatch between their genes and the environment in which they evolved. Humans are the most extreme example; maladaptation in modern society elevates risk of cancer, heart disease and psychological disorders (e.g., anxiety probably evolved to help escape p ....Evolutionary biomedicine: genetic pathologies as selection agents in three model systems. Our environment is changing at a rate never seen before, rendering organisms 'maladapted' if they cannot evolve quickly enough - that is, there will be a mismatch between their genes and the environment in which they evolved. Humans are the most extreme example; maladaptation in modern society elevates risk of cancer, heart disease and psychological disorders (e.g., anxiety probably evolved to help escape predators). I bring together two research areas that aim to explain what causes maladaptation - reproductive medicine and evolutionary biology. Results from this research will help us better understand genetic disease, future health hazards, and predict risk factors of extinction.Read moreRead less
An epigenetic basis for foetal programming. The social and economic impact of adult-onset diseases such as diabetes, hypertension and atherosclerosis is increasing. Evidence indicates that a mother's nutrition influences the risk of her children developing some diseases later in life. This proposal aims to elucidate the mechanism underlying this phenomenon. By understanding the mechanism through which maternal nutrition affects disease risk, we may make it possible to design early diagnosis and ....An epigenetic basis for foetal programming. The social and economic impact of adult-onset diseases such as diabetes, hypertension and atherosclerosis is increasing. Evidence indicates that a mother's nutrition influences the risk of her children developing some diseases later in life. This proposal aims to elucidate the mechanism underlying this phenomenon. By understanding the mechanism through which maternal nutrition affects disease risk, we may make it possible to design early diagnosis and intervention strategies. Our work may suggest intervention strategies - such as supplementation of at-risk mothers with key molecules such as methyl donors - during foetal and early postnatal life, which could be key to preventing premature morbidity and mortality.Read moreRead less
The role of dopamine in the regulation of worker sterility in the honey bee. This project will open new doors into the knowledge of honey bees' sterility. We will not only show that certain genes control honey bee sterility but also that there is interactions between these genes and environmental cues such as the pheromones released by the queen. The project will provide significant material for a better understanding of honey bees society. Honey bees remain the most important pollinator world w ....The role of dopamine in the regulation of worker sterility in the honey bee. This project will open new doors into the knowledge of honey bees' sterility. We will not only show that certain genes control honey bee sterility but also that there is interactions between these genes and environmental cues such as the pheromones released by the queen. The project will provide significant material for a better understanding of honey bees society. Honey bees remain the most important pollinator world wide, and their conservation is a major concern both to agriculturalists and the general public. The project will be of immense scientific interest, and likely to be regarded as a major breakthrough. The project will also foster a strong intellectual collaboration between New Zealand and Australia.Read moreRead less
Testing links between life-history and genome evolution. Chromosomes are fundamental units of inheritance. They often differ in number, size and structure between species, and may also differ between individuals within a species. The evolution of chromosomes is tied to that of organisms themselves, making them important for understanding the generation and maintenance of biodiversity. Yet, our understanding of the forces that influence chromosome evolution remains limited. This project will inve ....Testing links between life-history and genome evolution. Chromosomes are fundamental units of inheritance. They often differ in number, size and structure between species, and may also differ between individuals within a species. The evolution of chromosomes is tied to that of organisms themselves, making them important for understanding the generation and maintenance of biodiversity. Yet, our understanding of the forces that influence chromosome evolution remains limited. This project will investigate the formation of unusual chains of chromosomes that are increasingly being found in various vertebrate and invertebrate taxa, using an organism in which they are most commonly found: termites. We will test the hypothesis that inbreeding drives the evolution of meiotic sex linked chromosomes.Read moreRead less
How sexually antagonistic genes and sexual selection influence the evolution of the Y chromosome. Sexually antagonistic genes are beneficial to members of one sex, but costly to the other. They are of significance both to the coevolution between the sexes and the evolution of the sex chromosomes. We will measure the sexually antagonistic effects of genes that make male guppies sexually attractive. We will then study how these genes, and the process of sexual selection that favours them influence ....How sexually antagonistic genes and sexual selection influence the evolution of the Y chromosome. Sexually antagonistic genes are beneficial to members of one sex, but costly to the other. They are of significance both to the coevolution between the sexes and the evolution of the sex chromosomes. We will measure the sexually antagonistic effects of genes that make male guppies sexually attractive. We will then study how these genes, and the process of sexual selection that favours them influence the process of recombination between the X and Y chromosomes.Read moreRead less
Challenging current dogma on the inheritance of mitochondrial DNA. Mutations in mitochondrial DNA are often used to infer genetic relationships and have been associated with the expression of human diseases. This project examines the exact mechanism of inheritance of mitochondrial genes to enhance biological interpretations and our understanding of the heritability of specific diseases.
Additive and non-additive genetic benefits of mating behaviour: a synthesis of sexual selection and conservation genetics. This research will forge a synthesis between the study of mating behaviour and it's consequences (sexual selection) and the field of conservation genetics. It will have direct relevance to conservation attempts, and far-reaching implications for how we understand sexual behaviour and the complex mating decisions animals and humans make. The work will enhance Australia's stro ....Additive and non-additive genetic benefits of mating behaviour: a synthesis of sexual selection and conservation genetics. This research will forge a synthesis between the study of mating behaviour and it's consequences (sexual selection) and the field of conservation genetics. It will have direct relevance to conservation attempts, and far-reaching implications for how we understand sexual behaviour and the complex mating decisions animals and humans make. The work will enhance Australia's strong research reputation in evolutionary genetics, sexual selection and conservation biology.Read moreRead less
Linking mutant zebrafish phenotypes with their underlying genetic lesions. Zebrafish mutants have been generated with many interesting abnormalities, but to understand these abnormalities, the defective genes must be identified by positional cloning. We seek to identify the defective genes underpinning four mutants. Mutant #562 develops a normal nervous system which then undergoes rapid degeneration. The mutant flotte lotte has abnormal gut development. Two mutants with defective early blood for ....Linking mutant zebrafish phenotypes with their underlying genetic lesions. Zebrafish mutants have been generated with many interesting abnormalities, but to understand these abnormalities, the defective genes must be identified by positional cloning. We seek to identify the defective genes underpinning four mutants. Mutant #562 develops a normal nervous system which then undergoes rapid degeneration. The mutant flotte lotte has abnormal gut development. Two mutants with defective early blood formation will be studied. We will establish techniques for several steps that will be useful for all zebrafish mapping projects. We expect the genetic characterization of these mutants to provide new insights into nerve cell survival, gut development, and blood formation.Read moreRead less