Discovery Early Career Researcher Award - Grant ID: DE210100375
Funder
Australian Research Council
Funding Amount
$428,191.00
Summary
Defining single-strand DNA break repair capacity in oocytes. This project aims to investigate fundamental biological mechanisms required for the production of high-quality oocytes, which fortify female fertility and the propagation of all sexually reproducing species. Exploiting unique mouse models, this study will define the importance of single strand DNA break repair capacity in oocytes for the first time, by outlining the role of single strand DNA repair proteins in maintaining genetic integ ....Defining single-strand DNA break repair capacity in oocytes. This project aims to investigate fundamental biological mechanisms required for the production of high-quality oocytes, which fortify female fertility and the propagation of all sexually reproducing species. Exploiting unique mouse models, this study will define the importance of single strand DNA break repair capacity in oocytes for the first time, by outlining the role of single strand DNA repair proteins in maintaining genetic integrity of gametes throughout their lifespan. In doing so, the intended outcome of this project is to dramatically improve our understanding of quality control in the female germ line. This should provide significant benefits to Australia by positioning it as a world leader in the field of Reproductive Science.Read moreRead less
DNA repair: a critical quality control mechanism in the female germ line. This project aims to investigate the fundamental biological mechanisms required for the production of high quality gametes, which underpin female fertility and the propagation of all sexually reproducing species. By taking advantage of unique mouse and avian models, this project expects to define the role of the DNA repair protein TOP3A in the successful completion of meiosis and it's requirement for the survival and genet ....DNA repair: a critical quality control mechanism in the female germ line. This project aims to investigate the fundamental biological mechanisms required for the production of high quality gametes, which underpin female fertility and the propagation of all sexually reproducing species. By taking advantage of unique mouse and avian models, this project expects to define the role of the DNA repair protein TOP3A in the successful completion of meiosis and it's requirement for the survival and genetic integrity of gametes throughout their lifespan. In doing so, the intended outcome of this project is to dramatically improve our understanding of quality control in the female germ line. This should provide significant benefits to Australia by positioning it as a world leader in the field of Reproductive Science.Read moreRead less
Brain Regulation of Reproduction: Challenging the ‘KNDy’ Hypothesis. The brain switches reproduction on and off by changing the frequency of pulses of gonadotrophin releasing hormone. The processes that produce the pulses have been a puzzle for decades but, recently, brain cells that produce three peptides (kisspeptin, neurokinin B, dynorphin), known as ‘KNDy cells’, have been heralded as the ‘missing link’, or even the ‘pulse generator’. Using sheep, this project will challenge the KNDy hypothe ....Brain Regulation of Reproduction: Challenging the ‘KNDy’ Hypothesis. The brain switches reproduction on and off by changing the frequency of pulses of gonadotrophin releasing hormone. The processes that produce the pulses have been a puzzle for decades but, recently, brain cells that produce three peptides (kisspeptin, neurokinin B, dynorphin), known as ‘KNDy cells’, have been heralded as the ‘missing link’, or even the ‘pulse generator’. Using sheep, this project will challenge the KNDy hypothesis with pheromones and with acute increases in nutrition, two factors that rapidly increase the frequency of gonadotrophin releasing hormone pulses. The outcomes of this research are directly relevant to the optimisation of reproductive management in farm animals, wildlife and humans.Read moreRead less
The molecular basis of sperm competition. This project aims to unravel the molecular basis of reproductive conflicts. Males compete for paternity and this continues after mating if females copulate and receive semen from multiple males. In ants and bees, molecules in males’ ejaculates recognise and kill rival males’ sperm. Reproductive proteins in leaf cutter ants’ seminal fluid may be the molecular agents of sperm competition. This project will investigate reproductive proteins and their functi ....The molecular basis of sperm competition. This project aims to unravel the molecular basis of reproductive conflicts. Males compete for paternity and this continues after mating if females copulate and receive semen from multiple males. In ants and bees, molecules in males’ ejaculates recognise and kill rival males’ sperm. Reproductive proteins in leaf cutter ants’ seminal fluid may be the molecular agents of sperm competition. This project will investigate reproductive proteins and their functioning and effects on reproductive success. This project will show how reproductive conflicts over paternity operate on the protein level and may lead to novel avenues for future pest control.Read moreRead less
Evolutionary proteomics of social insects. This project aims to understand the molecular mechanisms that affect fertility in honeybees and leaf-cutting ants by identifying the function of proteins in male and female secretions related to insemination and sperm storage. The understanding of these general principles will have important applications for honeybee breeding.