53 research outputs found
A Design-based Research of an Oceanography Module as a Part of the Israeli High School Earth Sciences Program
This study is a Design-based Research type that was conducted in order to develop a new module: "Oceans and the Earth systems" as part of the environmental-based interdisciplinary component of the Israeli high school earth science curriculum. The study included three spiral cycles of development-implementation-research and the collection of the data was based on a battery of both qualitative and quantitative research tools. The sample included about 120 students from 8 classes from five different schools. The design-based research method enables to identify the strengths and the weaknesses of the curriculum in order to modify the curriculum. It was repeatedly found throughout the three development cycles that the interest of students in oceanography topics is high. The students have increased their knowledge significantly and undergone through a meaningful conceptual change. The students' achievements and attitudes correlated positively with the implementation of inquiry based learning in the lab and the outdoor learning environments, and the ability of the students to choose what they would like to study - all of it or at least part of it. Following our results it is suggested that the earth systems approach could serve as a powerful platform in motivating students to study complicated scientific concepts and processes from all the scientific disciplines
A New Approach to Garbled Circuits
A garbling scheme is a fundamental cryptographic building block with a long list of applications. The study of different techniques for garbling a function, towards optimizing computation and communication complexity, has been an area of active research. Most common garbling techniques work by representing each gate in the circuit as a set of ciphertexts that encrypt its truth table row-by-row.
In this work we present a new garbling scheme in the random oracle (RO) model that garbles circuits in the gate-by-gate paradigm by capturing the gate functionality (AND, XOR) as a whole rather than as a set of ciphertexts. The final gate garbling requires bits of communication in expectation, 4 RO calls for garbling and 1 RO call for evaluation. We prove that the scheme satisfies privacy in the non-programmable random oracle model and against PPT adversaries. We also show how this scheme can be extended to support free-XOR and garble any gate functionality over binary inputs
The dynamics between limited-term and lifelong coinfecting bacterial parasites in wild rodent hosts
The E3 Ubiquitin-Ligase Bmi1/Ring1A Controls the Proteasomal Degradation of Top2α Cleavage Complex â A Potentially New Drug Target
The topoisomerases Top1, Top2alpha and Top2beta are important molecular targets for antitumor drugs, which specifically poison Top1 or Top2 isomers. While it was previously demonstrated that poisoned Top1 and Top2beta are subject to proteasomal degradation, this phenomena was not demonstrated for Top2alpha.We show here that Top2alpha is subject to drug induced proteasomal degradation as well, although at a lower rate than Top2beta. Using an siRNA screen we identified Bmi1 and Ring1A as subunits of an E3 ubiquitin ligase involved in this process. We show that silencing of Bmi1 inhibits drug-induced Top2alpha degradation, increases the persistence of Top2alpha-DNA cleavage complex, and increases Top2 drug efficacy. The Bmi1/Ring1A ligase ubiquitinates Top2alpha in-vitro and cellular overexpression of Bmi1 increases drug induced Top2alpha ubiquitination. A small-molecular weight compound, identified in a screen for inhibitors of Bmi1/Ring1A ubiquitination activity, also prevents Top2alpha ubiquitination and drug-induced Top2alpha degradation. This ubiquitination inhibitor increases the efficacy of topoisomerase 2 poisons in a synergistic manner.The discovery that poisoned Top2alpha is undergoing proteasomal degradation combined with the involvement of Bmi1/Ring1A, allowed us to identify a small molecule that inhibits the degradation process. The Bmi1/Ring1A inhibitor sensitizes cells to Top2 drugs, suggesting that this type of drug combination will have a beneficial therapeutic outcome. As Bmi1 is also a known oncogene, elevated in numerous types of cancer, the identified Bmi1/Ring1A ubiquitin ligase inhibitors can also be potentially used to directly target the oncogenic properties of Bmi1
Recommended from our members
Publisher Correction: FGF signalling controls the specification of hair placode-derived SOX9 positive progenitors to Merkel cells.
The originally published version of this Article contained an error in Figure 2. In panel e, the blue bar was incorrectly labelled 'KRT8(+)/TOMATO(-)'. Furthermore, during the process of preparing a correction, the publication date of the Article was inadvertently changed to June 20th 2018. Both of these errors have been corrected in the PDF and HTML versions of the Article
FGF signalling controls the specification of hair placode-derived SOX9 positive progenitors to Merkel cells
Merkel cells are innervated mechanosensory cells responsible for light-touch sensations. In murine dorsal skin, Merkel cells are located in touch domes and found in the epidermis around primary hairs. While it has been shown that Merkel cells are skin epithelial cells, the progenitor cell population that gives rise to these cells is unknown. Here, we show that during embryogenesis, SOX9-positive (+) cells inside hair follicles, which were previously known to give rise to hair follicle stem cells (HFSCs) and cells of the hair follicle lineage, can also give rise to Merkel Cells. Interestingly, while SOX9 is critical for HFSC specification, it is dispensable for Merkel cell formation. Conversely, FGFR2 is required for Merkel cell formation but is dispensable for HFSCs. Together, our studies uncover SOX9(+) cells as precursors of Merkel cells and show the requirement for FGFR2-mediated epithelial signalling in Merkel cell specification.Peer reviewe
PRC1 fine-tunes gene repression and activation to safeguard skin development and stem cell specification
Path analyses of cross-sectional and longitudinal data suggest that variability in natural communities of blood-associated parasites is derived from host characteristics and not interspecific interactions
Abstract Background The parasite composition of wild host individuals often impacts their behavior and physiology, and the transmission dynamics of pathogenic species thereby determines disease risk in natural communities. Yet, the determinants of parasite composition in natural communities are still obscure. In particular, three fundamental questions remain open: (1) what are the relative roles of host and environmental characteristics compared with direct interactions between parasites in determining the community composition of parasites? (2) do these determinants affect parasites belonging to the same guild and those belonging to different guilds in similar manners? and (3) can cross-sectional and longitudinal analyses work interchangeably in detecting community determinants? Our study was designed to answer these three questions in a natural community of rodents and their fleas, ticks, and two vector-borne bacteria. Methods We sampled a natural population of Gerbillus andersoni rodents and their blood-associated parasites on two occasions. By combining path analysis and model selection approaches, we then explored multiple direct and indirect paths that connect (i) the environmental and host-related characteristics to the infection probability of a host by each of the four parasite species, and (ii) the infection probabilities of the four species by each other. Results Our results suggest that the majority of paths shaping the blood-associated communities are indirect, mostly determined by host characteristics and not by interspecific interactions or environmental conditions. The exact effects of host characteristics on infection probability by a given parasite depend on its life history and on the method of sampling, in which the cross-sectional and longitudinal methods are complementary. Conclusions Despite the awareness of the need of ecological investigations into natural host-vector-parasite communities in light of the emergence and re-emergence of vector-borne diseases, we lack sampling methods that are both practical and reliable. Here we illustrated how comprehensive patterns can be revealed from observational data by applying path analysis and model selection approaches and combining cross-sectional and longitudinal analyses. By employing this combined approach on blood-associated parasites, we were able to distinguish between direct and indirect effects and to predict the causal relationships between host-related characteristics and the parasite composition over time and space. We concluded that direct interactions within the community play only a minor role in determining community composition relative to host characteristics and the life history of the community members
The minimum length of a base for the symmetric group acting on partitions
A base for a permutation group, G, is a sequence of elements of its permutation domain whose stabiliser in G is trivial. Using purely elementary and constructive methods, we obtain bounds on the minimum length of a base for the action of the symmetric group on partitions of a set into blocks of equal size. This upper bound is a constant when the size of each block is at most equal to the number of blocks and logarithmic in the size of a block otherwise. These bounds are asymptotically best possible
Similarities and seasonal variations in bacterial communities from the blood of rodents and from their flea vectors
Vector-borne microbes are subject to the ecological constraints of two distinct microenvironments: that in the arthropod vector and that in the blood of its vertebrate host. Because the structure of bacterial communities in these two microenvironments may substantially affect the abundance of vector-borne microbes, it is important to understand the relationship between bacterial communities in both microenvironments and the determinants that shape them. We used pyrosequencing analyses to compare the structure of bacterial communities in Synosternus cleopatrae fleas and in the blood of their Gerbillus andersoni hosts. We also monitored the interindividual and seasonal variability in these bacterial communities by sampling the same individual wild rodents during the spring and again during the summer. We show that the bacterial communities in each sample type (blood, female flea or male flea) had a similar phylotype composition among host individuals, but exhibited seasonal variability that was not directly associated with host characteristics. The structure of bacterial communities in male fleas and in the blood of their rodent hosts was remarkably similar and was dominated by flea-borne Bartonella and Mycoplasma phylotypes. A lower abundance of flea-borne bacteria and the presence of Wolbachia phylotypes distinguished bacterial communities in female fleas from those in male fleas and in rodent blood. These results suggest that the overall abundance of a certain vector-borne microbe is more likely to be determined by the abundance of endosymbiotic bacteria in the vector, abundance of other vector-borne microbes co-occurring in the vector and in the host blood and by seasonal changes, than by host characteristics
- âŠ