School of BioSciences - Research Publications

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    HBO1 (KAT7) Does Not Have an Essential Role in Cell Proliferation, DNA Replication, or Histone 4 Acetylation in Human Cells
    Kueh, AJ ; Eccles, S ; Tang, L ; Garnham, AL ; May, RE ; Herold, MJ ; Smyth, GK ; Voss, AK ; Thomas, T (American Society for Microbiology, 2020-02-01)
    HBO1 (MYST2/KAT7) is essential for histone 3 lysine 14 acetylation (H3K14ac) but is dispensable for H4 acetylation and DNA replication in mouse tissues. In contrast, previous studies using small interfering RNA (siRNA) knockdown in human cell lines have suggested that HBO1 is essential for DNA replication. To determine if HBO1 has distinctly different roles in immortalized human cell lines and normal mouse cells, we performed siRNA knockdown of HBO1. In addition, we used CRISPR/Cas9 to generate 293T, MCF7, and HeLa cell lines lacking HBO1. Using both techniques, we show that HBO1 is essential for all H3K14ac in human cells and is unlikely to have a direct effect on H4 acetylation and only has minor effects on cell proliferation. Surprisingly, the loss of HBO1 and H3K14ac in HeLa cells led to the secondary loss of almost all H4 acetylation after 4 weeks. Thus, HBO1 is dispensable for DNA replication and cell proliferation in immortalized human cells. However, while cell proliferation proceeded without HBO1 and H3K14ac, HBO1 gene deletion led to profound changes in cell adhesion, particularly in 293T cells. Consistent with this phenotype, the loss of HBO1 in both 293T and HeLa principally affected genes mediating cell adhesion, with comparatively minor effects on other cellular processes.
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    Assessment and management of reproduction in Australian monotremes and marsupials
    Keeley, T ; Johnston, S ; Vogelnest, L ; Portas, T (CSIRO Publishing, 2019)
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    Males evolve to be more harmful under increased sexual conflict intensity in a seed beetle
    McNamara, KB ; Sloan, NS ; Kershaw, SE ; Van Lieshout, E ; Simmons, LW ; Smiseth, P (OXFORD UNIV PRESS INC, 2020-01-28)
    One conspicuous manifestation of sexual conflict is traumatic mating, in which male genitalia damage the female during copulation. The penis of the seed beetle, Callosobruchus maculatus, is covered in spines that damage the female reproductive tract. Females kick males ostensibly to shorten these harmful copulations. How these iconic conflict behaviors coevolve in response to sexual conflict intensity can provide insight into the economics of these traits. We examined whether male harm and female resistance coevolved in response to elevated sexual conflict. We quantified copulation behavior and female reproductive tract damage of individuals from replicated populations evolving for 32 generations under low or high sexual conflict (female- and male-biased treatments, respectively). First, we permitted females ad libitum matings with males from either sex-ratio treatment, recording her tract damage and longevity. Second, we performed a full-factorial cross of matings by males and females from each of the replicate populations, recording mating and kicking duration and reproductive output. We found manipulation of sexual conflict intensity led to the evolution of male harmfulness, but not female resistance to harm. We also demonstrate that female kicking does not respond to sexual conflict intensity, suggesting it does not function to mitigate male harm in this species. Our findings demonstrate the complexities of behavioral and morphological coevolutionary responses to sexual conflict intensity in an important model species.
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    Socially cued anticipatory adjustment of female signalling effort in a moth
    Pham, HT ; McNamara, KB ; Elgar, MA (The Royal Society Publishing, 2020-12-23)
    Juvenile population density has profound effects on subsequent adult development, morphology and reproductive investment. Yet, little is known about how the juvenile social environment affects adult investment into chemical sexual signalling. Male gumleaf skeletonizer moths, Uraba lugens, facultatively increase investment into antennae (pheromone receiving structures) when reared at low juvenile population densities, but whether there is comparable adjustment by females into pheromone investment is not known. We investigate how juvenile population density influences the ‘calling' (pheromone-releasing) behaviour of females and the attractiveness of their pheromones. Female U. lugens adjust their calling behaviour in response to socio-sexual cues: adult females reared in high juvenile population densities called earlier and for longer than those from low juvenile densities. Juvenile density also affected female pheromonal attractiveness: Y-maze olfactometer assays revealed that males prefer pheromones produced by females reared at high juvenile densities. This strategic investment in calling behaviour by females, based on juvenile cues that anticipate the future socio-sexual environment, likely reflects a response to avoid mating failure through competition with neighbouring signallers.
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    Characterization of the apicoplast-localized enzyme TgUroD in Toxoplasma gondii reveals a key role of the apicoplast in heme biosynthesis
    Tjhin, ET ; Hayward, JA ; Mcfadden, G ; van Dooren, GG (ELSEVIER, 2020-02-07)
    Apicomplexan parasites such as Toxoplasma gondii possess an unusual heme biosynthesis pathway whose enzymes localize to the mitochondrion, cytosol, or apicoplast, a nonphotosynthetic plastid present in most apicomplexans. To characterize the involvement of the apicoplast in the T. gondii heme biosynthesis pathway, we investigated the role of the apicoplast-localized enzyme uroporphyrinogen III decarboxylase (TgUroD). We found that TgUroD knockdown impaired parasite proliferation, decreased free heme levels in the parasite, and decreased the abundance of heme-containing c-type cytochrome proteins in the parasite mitochondrion. We validated the effects of heme loss on mitochondrial cytochromes by knocking down cytochrome c/c1 heme lyase 1 (TgCCHL1), a mitochondrial enzyme that catalyzes the covalent attachment of heme to c-type cytochromes. TgCCHL1 depletion reduced parasite proliferation and decreased the abundance of c-type cytochromes. We further sought to characterize the overall importance of TgUroD and TgCCHL1 for both mitochondrial and general parasite metabolism. TgUroD depletion decreased cellular ATP levels, mitochondrial oxygen consumption, and extracellular acidification rates. By contrast, depletion of TgCCHL1 neither diminished ATP levels in the parasite nor impaired extracellular acidification rate, but resulted in specific defects in mitochondrial oxygen consumption. Together, our results indicate that the apicoplast has a key role in heme biology in T. gondii and is important for both mitochondrial and general parasite metabolism. Our study highlights the importance of heme and its synthesis in these parasites.
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    Conserved Glu-47 and Lys-50 residues are critical for UDP-N-acetylglucosamine/UMP antiport activity of the mouse Golgi-associated transporter Slc35a3
    Agustina Toscanini, M ; Belen Favarolo, M ; Gonzalez Flecha, FL ; Ebert, B ; Rautengarten, C ; Bredeston, LM (AMER SOC BIOCHEMISTRY MOLECULAR BIOLOGY INC, 2019-06-28)
    Nucleotide sugar transporters (NSTs) regulate the flux of activated sugars from the cytosol into the lumen of the Golgi apparatus where glycosyltransferases use them for the modification of proteins, lipids, and proteoglycans. It has been well-established that NSTs are antiporters that exchange nucleotide sugars with the respective nucleoside monophosphate. Nevertheless, information about the molecular basis of ligand recognition and transport is scarce. Here, using topology predictors, cysteine-scanning mutagenesis, expression of GFP-tagged protein variants, and phenotypic complementation of the yeast strain Kl3, we identified residues involved in the activity of a mouse UDP-GlcNAc transporter, murine solute carrier family 35 member A3 (mSlc35a3). We specifically focused on the putative transmembrane helix 2 (TMH2) and observed that cells expressing E47C or K50C mSlc35a3 variants had lower levels of GlcNAc-containing glycoconjugates than WT cells, indicating impaired UDP-GlcNAc transport activity of these two variants. A conservative substitution analysis revealed that single or double substitutions of Glu-47 and Lys-50 do not restore GlcNAc glycoconjugates. Analysis of mSlc35a3 and its genetic variants reconstituted into proteoliposomes disclosed the following: (i) all variants act as UDP-GlcNAc/UMP antiporters; (ii) conservative substitutions (E47D, E47Q, K50R, or K50H) impair UDP-GlcNAc uptake; and (iii) substitutions of Glu-47 and Lys-50 dramatically alter kinetic parameters, consistent with a critical role of these two residues in mSlc35a3 function. A bioinformatics analysis revealed that an EXXK motif in TMH2 is highly conserved across SLC35 A subfamily members, and a 3D-homology model predicted that Glu-47 and Lys-50 are facing the central cavity of the protein.
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    Cost-benefit analysis of the yellow crazy ant eradication program. Technical Report prepared for the Wet Tropics Management Authority
    Spring, D ; Kompas, T ; Bradhurst, R (Centre of Excellence for Biosecurity Risk Analysis, 2019)
    Yellow crazy ants (Anoplolepis gracilipes) (YCA) are one of the world’s 100 worst invasive species (Lowe et al. 2000). Previous assessments of YCA invasions have demonstrated that YCA can dramatically reduce native species richness in invaded areas, including in the Seychelles (Bos et al. 2008), Christmas Island (O'Dowd et al. 2003), and Hawaii (Plentovich et al. 2011). Native species losses include direct losses of competing invertebrate species and indirect losses resulting from ecological interdependencies, which can result in “ecological meltdown” in extreme cases such as Christmas Island (O'Dowd et al. 2003). YCA can also cause large losses to people living in infested areas through nuisance and health effects (Lach and Hoskin 2015) and can also adversely affect agricultural producers (Young et al. 2001) through reducing yields and/or increasing pesticide costs. YCA was first detected in Cairns and its southern suburbs in 2001, and an eradication program was initiated by the Department of Natural Resources and Mines (DNRM) and Biosecurity Queensland as part of a larger state-wide program. Later discoveries of YCA across the state, including in and around the WTWHA led to the state-wide eradication program being discontinued. An application was then made by WTMA to continue eradication efforts in and around the WTWHA. The program has been funded by the Australian Government and the Queensland Government in two overlapping projects, as described in the Executive Summary.
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    Widespread cis-regulatory convergence between the extinct Tasmanian tiger and gray wolf
    Feigin, CY ; Newton, AH ; Pask, AJ (COLD SPRING HARBOR LAB PRESS, PUBLICATIONS DEPT, 2019-10)
    The extinct marsupial Tasmanian tiger, or thylacine, and the eutherian gray wolf are among the most widely recognized examples of convergent evolution in mammals. Despite being distantly related, these large predators independently evolved extremely similar craniofacial morphologies, and evidence suggests that they filled similar ecological niches. Previous analyses revealed little evidence of adaptive convergence between their protein-coding genes. Thus, the genetic basis of their convergence is still unclear. Here, we identified candidate craniofacial cis-regulatory elements across vertebrates and compared their evolutionary rates in the thylacine and wolf, revealing abundant signatures of convergent positive selection. Craniofacial thylacine-wolf accelerated regions were enriched near genes involved in TGF beta (TGFB) and BMP signaling, both of which are key morphological signaling pathways with critical roles in establishing the identities and boundaries between craniofacial tissues. Similarly, enhancers of genes involved in craniofacial nerve development showed convergent selection and involvement in these pathways. Taken together, these results suggest that adaptation in cis-regulators of TGF beta and BMP signaling may provide a mechanism to explain the coevolution of developmentally and functionally integrated craniofacial structures in these species. We also found that despite major structural differences in marsupial and eutherian brains, accelerated regions in both species were common near genes with roles in brain development. Our findings support the hypothesis that, relative to protein-coding genes, positive selection on cis-regulatory elements is likely to be an essential driver of adaptive convergent evolution and may underpin thylacine-wolf phenotypic similarities.
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    Stevens-Johnson Syndrome complicated by obstructive uropathy, pneumothorax, and pneumomediastinum: a case report and literature review
    Bruce-Hickman, D ; Jiang, X ; Thia, JJ-P ; Kansal, A (BMC, 2019-06-11)
    BACKGROUND: Stevens-Johnson Syndrome (SJS) is an acute mucocutaneous eruption with blisters of the skin and haemorrhagic erosions of mucous membranes. This report describes air-leak syndrome and obstructive uropathy occurring simultaneously in a teenage patient affected by SJS. CASE PRESENTATION: A 17-year-old Malay female with SJS suffered from bilateral pneumothoraces, pneumomediastinum, and obstructive uropathy as early complications of her disease. She required intubation, chest tube insertion, and bilateral ureteric stenting as part of her intensive care management. These extra-cutaneous complications of renal and pulmonary systems were likely secondary to widespread epithelial detachment. CONCLUSION: Despite paucity of cases in adult literature, post-renal causes for acute kidney injury must be considered in SJS, especially in the setting of gross haematuria. Bedside point-of-care ultrasonography may be a useful tool for excluding obstructive uropathy. Pneumothorax is a rare but documented complication of SJS in paediatric cases and, to a lesser extent, adult patients. Extra care should be exercised when caring for mechanically ventilated patients suffering from SJS.
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    Integrating the underlying structure of stochasticity into community ecology
    Shoemaker, LG ; Sullivan, LL ; Donohue, I ; Cabral, JS ; Williams, RJ ; Mayfield, MM ; Chase, JM ; Chu, C ; Harpole, WS ; Huth, A ; HilleRisLambers, J ; James, ARM ; Kraft, NJB ; May, F ; Muthukrishnan, R ; Satterlee, S ; Taubert, F ; Wang, X ; Wiegand, T ; Yang, Q ; Abbott, KC (WILEY, 2020-02)
    Stochasticity is a core component of ecology, as it underlies key processes that structure and create variability in nature. Despite its fundamental importance in ecological systems, the concept is often treated as synonymous with unpredictability in community ecology, and studies tend to focus on single forms of stochasticity rather than taking a more holistic view. This has led to multiple narratives for how stochasticity mediates community dynamics. Here, we present a framework that describes how different forms of stochasticity (notably demographic and environmental stochasticity) combine to provide underlying and predictable structure in diverse communities. This framework builds on the deep ecological understanding of stochastic processes acting at individual and population levels and in modules of a few interacting species. We support our framework with a mathematical model that we use to synthesize key literature, demonstrating that stochasticity is more than simple uncertainty. Rather, stochasticity has profound and predictable effects on community dynamics that are critical for understanding how diversity is maintained. We propose next steps that ecologists might use to explore the role of stochasticity for structuring communities in theoretical and empirical systems, and thereby enhance our understanding of community dynamics.