66 research outputs found

    Vol.2 Cha.10 Twenty-first Century Hopewell

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    https://ideaexchange.uakron.edu/encountering_hopewell/1020/thumbnail.jp

    The Manring Mounds: A Hopewell Center in the Mad River Drainage, Clark County, Ohio

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    Author Institution: Department of Sociology and Anthropology, Kent State UniversityThe Manring archaeological site is a Hopewell center located on Beaver Creek, a tributary of the Mad River, in Clark County, Ohio. Comparisons with other excavated sites show the Manring site to represent a substantial labor commitment; it includes one of the very largest known Hopewell mounds. The presence of such exotica as an obsidian spear, a copper breastplate, copper celts and marine shell beads are also noteworthy, especially given the site's hinterland location. The juxtaposition of major routes of travel is suggested to be a more important factor in explaining site location than any direct subsistence advantage. Cross-dating indicates that Manring was occupied shortly after A. D. 100, or coincident with the early Pike phase as defined in the Illinois Valley

    Vol. 2 Ch. 5 Scale and Community in Hopewell Networks (SCHoN): Summary of Preliminary Results

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    https://ideaexchange.uakron.edu/encountering_hopewell/1015/thumbnail.jp

    Vol. 2 Ch. 4 Material Choice and Interaction on Brown\u27s Bottom

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    https://ideaexchange.uakron.edu/encountering_hopewell/1014/thumbnail.jp

    Reverse Effect of Mammalian Hypocalcemic Cortisol in Fish: Cortisol Stimulates Ca2+ Uptake via Glucocorticoid Receptor-Mediated Vitamin D3 Metabolism

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    Cortisol was reported to downregulate body-fluid Ca2+ levels in mammals but was proposed to show hypercalcemic effects in teleostean fish. Fish, unlike terrestrial vertebrates, obtain Ca2+ from the environment mainly via the gills and skin rather than by dietary means, and have to regulate the Ca2+ uptake functions to cope with fluctuating Ca2+ levels in aquatic environments. Cortisol was previously found to regulate Ca2+ uptake in fish; however, the molecular mechanism behind this is largely unclear. Zebrafish were used as a model to explore this issue. Acclimation to low-Ca2+ fresh water stimulated Ca2+ influx and expression of epithelial calcium channel (ecac), 11β-hydroxylase and the glucocorticoid receptor (gr). Exogenous cortisol increased Ca2+ influx and the expressions of ecac and hydroxysteroid 11-beta dehydrogenase 2 (hsd11b2), but downregulated 11β-hydroxylase and the gr with no effects on other Ca2+ transporters or the mineralocorticoid receptor (mr). Morpholino knockdown of the GR, but not the MR, was found to impair zebrafish Ca2+ uptake function by inhibiting the ecac expression. To further explore the regulatory mechanism of cortisol in Ca2+ uptake, the involvement of vitamin D3 was analyzed. Cortisol stimulated expressions of vitamin D-25hydroxylase (cyp27a1), cyp27a1 like (cyp27a1l), 1α-OHase (cyp27b1) at 3 dpf through GR, the first time to demonstrate the relationship between cortisol and vitamin D3 in fish. In conclusion, cortisol stimulates ecac expression to enhance Ca2+ uptake functions, and this control pathway is suggested to be mediated by the GR. Lastly, cortisol also could mediate vitamin D3 signaling to stimulate Ca2+ uptake in zebrafish

    Tailor-Made Zinc-Finger Transcription Factors Activate FLO11 Gene Expression with Phenotypic Consequences in the Yeast Saccharomyces cerevisiae

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    Cys2His2 zinc fingers are eukaryotic DNA-binding motifs, capable of distinguishing different DNA sequences, and are suitable for engineering artificial transcription factors. In this work, we used the budding yeast Saccharomyces cerevisiae to study the ability of tailor-made zinc finger proteins to activate the expression of the FLO11 gene, with phenotypic consequences. Two three-finger peptides were identified, recognizing sites from the 5′ UTR of the FLO11 gene with nanomolar DNA-binding affinity. The three-finger domains and their combined six-finger motif, recognizing an 18-bp site, were fused to the activation domain of VP16 or VP64. These transcription factor constructs retained their DNA-binding ability, with the six-finger ones being the highest in affinity. However, when expressed in haploid yeast cells, only one three-finger recombinant transcription factor was able to activate the expression of FLO11 efficiently. Unlike in the wild-type, cells with such transcriptional activation displayed invasive growth and biofilm formation, without any requirement for glucose depletion. The VP16 and VP64 domains appeared to act equally well in the activation of FLO11 expression, with comparable effects in phenotypic alteration. We conclude that the functional activity of tailor-made transcription factors in cells is not easily predicted by the in vitro DNA-binding activity
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