Anti-GST tag antibody [PerCP]

Ground stone tool (GST) technology includes artefacts utilized in pounding or grinding activities and characterized by long life cycles and multiple uses. The introduction of such technology dates back to early prehistory, and for this reason, it is used as prime evidence for tackling a wide range of archaeological questions such as the origins of technology, patterns of daily subsistence and lifeways. In this paper, we contribute to the field of study of GSTs by discussing the application of a novel multi-level analytical approach combining use wear and residue observations at low and high magnification with residue spatial distribution investigated using GIS. We aim to assess the potential of a combined use wear and residue approach to (1) discriminate specific gestures and worked materials on sandstone GSTs and (2) understand the potential of residue distributions for reconstructing ancient GST functions and, more specifically, the role of GSTs recovered at Mesolithic sites of the Danube Gorges region in the Central Balkans. We identified diagnostic surface modifications associated with the use of GSTs in different activities involving both animal and plant materials. Morphological characteristics of residues have been described under reflected and transmitted light and characterized using biochemical staining. Finally, we mapped residues across the utilized surfaces of experimental tools to link patterns of residue spatial distribution to specific materials and gestures. We expect our methodological approach will be taken up by other researchers in order to produce comparable datasets on GSTs and improve our understanding of their ancient functional biographies.

Epilepsy affects millions of individuals worldwide and many cases are pharmacoresistant. Duplication 15q syndrome (Dup25q) is a genetic disorder caused by duplications of the 15q11.2-q13.1 region. Phenotypes include a high rate of pharmacoresistant epilepsy. We developed a Dup15q model in Drosophila melanogaster that recapitulates seizures in Dup15q by over-expressing fly Dube3a or human UBE3A in glial cells, but not neurons, implicating glia in the Dup15q epilepsy phenotype. We compared Dube3a overexpression in glia (repo > Dube3a) versus neurons (elav > Dube3a) using transcriptomics and proteomics of whole fly head extracts. We identified 851 transcripts differentially regulated in repo > Dube3a, including an upregulation of glutathione S-transferase (GST) genes that occurred cell autonomously within glial cells. We reliably measured approximately 2,500 proteins by proteomics, most of which were also quantified at the transcript level. Combined transcriptomic and proteomic analysis revealed an enrichment of 21 synaptic transmission genes downregulated at the transcript and protein in repo > Dube3a indicating synaptic proteins change in a cell non-autonomous manner in repo > Dube3a flies. We identified 6 additional glia originating bang-sensitive seizure lines and found upregulation of GSTs in 4 out of these 6 lines. These data suggest GST upregulation is common among gliopathic seizures and may ultimately provide insight for treating epilepsy.