8 research outputs found

    Understanding how the chloroplasts contribute to wheat susceptibility to rust fungi

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    Wheat rust fungi of the Pucciniaceae family, including Puccinia striiformis f. sp. tritici (Pst), pose a significant and sustained threat to global wheat production. Previous research has shown that yield losses associated with wheat rust infection primarily result from a reduction in the photosynthetic capacity of the plant. Additionally, it is widely understood that the chloroplasts are a hub for the synthesis and release of a number of pro-defence molecules including reactive oxygen species, calcium ions and salicylic acid, making them important organelles for coordinating the immune response. However, the molecular details of how chloroplast processes are manipulated during wheat infection with rust fungi remain to be elucidated. The main objective of this project was to investigate the ways in which wheat chloroplast processes contribute to rust susceptibility. To this aim, RNA-sequencing was carried out prior to the onset of this project on Pst-infected wheat tissue over time, revealing that many nuclear genes encoding chloroplast-localised proteins (NGCPs) had expression patterns that correlate with resistance to Pst at later stages of infection. I then selected the chloroplast metallopeptidase of unknown function (TaCPEP), which followed this pattern of expression, for further analyses. We obtained disruption mutants from a tetraploid and hexaploid Targeted Induced Local Lesions In Genomes (TILLING) population and showed that TaCPEP disruption increases susceptibility to both Pst and Magnaporthe oryzae pathotype triticum and may reduce chlorophyll content and chloroplast size, but without affecting the rate of assimilation. This thesis provides insight into the ways in which chloroplastic processes are altered during wheat infection with Pst and how one gene specifically may play a key role in susceptibility

    Nanofibrous scaffolds releasing a small molecule BDNF-mimetic for the re-direction of endogenous neuroblast migration in the brain

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    9siBrain tissue engineering has the potential to harness existing elements of neurogenesis within the adult brain to overcome a microenvironment that is otherwise inhibitory to regeneration, especially following severe tissue damage. This study investigates the ability of electrospun poly ε-caprolactone (PCL) to re-direct the migratory pathway of endogenous neuroblasts from the disrupted subventricular zone (SVZ). A small molecule non-peptide ligand (BDNF-mimetic) that mimicked the trophic properties of brain-derived neurotrophic factor (BDNF) was incorporated into electrospun PCL scaffolds to improve neuroblast survival and promote neuroblast migration towards the implant. PCL scaffolds were able to support neuroblast infiltration and migration along the implant tract. In the presence of the BDNF-mimetic, neuroblasts were able to migrate towards the implant via the parenchyma, and their persistence within the implants was prolonged. In addition, the BDNF-mimetic improved implant integration and increased local neuronal plasticity by increasing neurite sprouting at the tissue-implant interface. SMI32+ neurites were observed inside scaffolds at 21 days but not 8 days post implantation, indicating that at least some of the infiltrated neuroblasts had differentiated into neurons.nonenoneFon, Deniece; Zhou, Kun; Ercole, Francesca; Fehr, Friederike; Marchesan, Silvia; Minter, Myles R.; Crack, Peter J.; Finkelstein, David I.; Forsythe, John SFon, Deniece; Zhou, Kun; Ercole, Francesca; Fehr, Friederike; Marchesan, Silvia; Minter, Myles R.; Crack, Peter J.; Finkelstein, David I.; Forsythe, John S
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