Goldstone Theorem in the Gaussian Functional Approximation to the Scalar ϕ4\phi^{4} Theory

We verify the Goldstone theorem in the Gaussian functional approximation to the $\phi^{4}$ theory with internal O(2) symmetry. We do so by reformulating the Gaussian approximation in terms of Schwinger-Dyson equations from which an explicit demonstration of the Goldstone theorem follows directly.Comment: 11 page

Objective measurement of habitual sedentary behavior in pre-school children: comparison of activPAL with actigraph monitors

The Actigraph is well established for measurement of both physical activity and sedentary behavior in children. The activPAL is being used increasingly in children, though with no published evidence on its use in free-living children to date. The present study compared the two monitors in preschool children. Children (n 23) wore both monitors simultaneously during waking hours for 5.6d and 10h/d. Daily mean percentage of time sedentary (nontranslocation of the trunk) was 74.6 (SD 6.8) for the Actigraph and 78.9 (SD 4.3) for activPAL. Daily mean percentage of time physically active (light intensity physical activity plus MVPA) was 25.4 (SD 6.8) for the Actigraph and 21.1 (SD 4.3) for the activPAL. Bland-Altman tests and paired t tests suggested small but statistically significant differences between the two monitors. Actigraph and activPAL estimates of sedentary behaviour and physical activity in young children are similar at a group level

Metabolic engineering approaches to biosynthesize terpenoids in Saccharomyces cerevisiae

Terpenoids are the largest class of natural products and are typically isolated from natural sources. However, heterologous expression of terpene synthases in microbial hosts such as E. coli or Saccharomyces cerevisiae has become an attractive alternative. S. cerevisiae has an intact sterol biosynthetic pathway, and many of the intermediates also serve as precursors for terpene synthases. Metabolic engineering efforts focus on optimizing product yields through increasing carbon flux through the desired pathway, removing competing enzymes, or altering enzymatic activity. This work describes the metabolic engineering of S. cerevisiae to enhance terpene production by exploiting these three approaches. Diterpene synthases were expressed in a yeast strain previously reported to accumulate the diterpene precursor geranylgeranyl pyrophosphate (GGPP). The strains produced milligram amounts of GGPP hydrolysis products geranylgeraniol and geranyllinalool, as well as the GGPP cyclization products ent -copalyl pyrophosphate, ent-kaurene, and abietadiene. Because diterpene production is limited by transit peptides targeting diterpene synthases into plastids, protein expression was increased by co-expressing a chloroplast processing enzyme in two different diterpene-producing strains. The in vivo-generated mature diterpene synthases functioned more effectively, thereby increasing cyclization yield. This thesis also describes a new method for controlling farnesyl pyrophosphate (FPP) hydrolysis product profile by adjusting media pH. Hydrolysis was found to be partially controlled by a phosphatase DPP1, however a majority of FPP hydrolysis is non-enzymatic. In a squalene synthase deletion strain, FPP accumulates and hydrolyzes readily to farnesol and nerolidol, and the ratios of these products are determined by the pH of the media. Finally, a yeast strain was constructed to increase production of the 30-carbon triterpene precursors oxidosqualene (OS) and dioxidosqualene (DOS) by over-expressing the sterol biosynthesis rate-limiting enzyme 3-hydroxy-3-methylglutaryl CoA reductase (HMG1) in a lanosterol synthase deletion background. This strain accumulated twenty times more OS and DOS than the strain with only the native HMG1. Over-expression of squalene epoxidase (ERG1) in a lanosterol synthase background greatly enhanced the levels of DOS compared to OS

Induced P-wave Superfluidity in Asymmetric Fermi Gases

We show that two new intra-species P-wave superfluid phases appear in two-component asymmetric Fermi systems with short-range S-wave interactions. In the BEC limit, phonons of the molecular BEC induce P-wave superfluidity in the excess fermions. In the BCS limit, density fluctuations induce P-wave superfluidity in both the majority and the minority species. These phases may be realized in experiments with spin-polarized Fermi gases.Comment: published versio

Using Health Care Utilization and Publication Patterns to Characterize the Research Portfolio and to Plan Future Research Investments

Objective: Government funders of biomedical research are under increasing pressure to demonstrate societal benefits of their investments. A number of published studies attempted to correlate research funding levels with the societal burden for various diseases, with mixed results. We examined whether research funded by the Department of Veterans Affairs (VA) is well aligned with current and projected veterans’ health needs. The organizational structure of the VA makes it a particularly suitable setting for examining these questions. Methods: We used the publication patterns and dollar expenditures of VA-funded researchers to characterize the VA research portfolio by disease. We used health care utilization data from the VA for the same diseases to define veterans’ health needs. We then measured the level of correlation between the two and identified disease groups that were under- or over-represented in the research portfolio relative to disease expenditures. Finally, we used historic health care utilization trends combined with demographic projections to identify diseases and conditions that are increasing in costs and/or patient volume and consequently represent potential targets for future research investments. Results: We found a significant correlation between research volume/expenditures and health utilization. Some disease groups were slightly under- or over-represented, but these deviations were relatively small. Diseases and conditions with the increasing utilization trend at the VA included hypertension, hypercholesterolemia, diabetes, hearing loss, sleeping disorders, complications of pregnancy, and several mental disorders. Conclusions: Research investments at the VA are well aligned with veteran health needs. The VA can continue to meet these needs by supporting research on the diseases and conditions with a growing number of patients, costs of care, or both. Our approach can be used by other funders of disease research to characterize their portfolios and to plan research investments

Gα13 Mediates a Signal That Is Essential for Proliferation and Survival of Thymocyte Progenitors

G protein signaling via the Gα12 family (Gα12 and Gα13) has not been well studied in T cells. To investigate whether Gα12 and Gα13 are involved in thymopoiesis, we expressed the regulator of G protein signaling domain of p115RhoGEF to inhibit Gα12 and Gα13 during thymopoiesis. Fetal thymus organ cultures seeded with p115ΔDH-expressing progenitor cells showed impaired thymopoiesis with a block at the CD4−CD8−CD44−CD25+ (DN3) stage. Using Gα13 or Gα12 minigenes, we demonstrated that Gα13, but not Gα12, is required for thymopoiesis. T progenitor cells expressing p115ΔDH showed reduced proliferation and increased cell death. T cell receptor stimulation of the fetal thymus organ cultures did not rescue the block. Overexpression of the antiapoptotic gene Bcl2 rescued the defect in DN3 cells and partially rescued T cell development. Therefore, Gα13-mediated signaling is necessary in early thymocyte proliferation and survival

TSLP is involved in expansion of early thymocyte progenitors

© 2007 Jiang et al; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution Licens

Elastic Nd scattering at intermediate energies as a tool for probing the short-range deuteron structure

A calculation of the deuteron polarization observables $A^d_y$, $A_{yy}$, $A_{xx}$, $A_{xz}$ and the differential cross-section for elastic nucleon-deuteron scattering at incident deuteron energies 270 and 880 MeV in lab is presented. A comparison of the calculations with two different deuteron wave-functions derived from the Bonn-CD $NN$-potential model and the dressed bag quark model is carried out. A model-independent approach, based on an optical potential framework, is used in which a nucleon-nucleon $T$-matrix is assumed to be local and taken on the energy shell, but still depends on the internal nucleon momentum in a deuteron.Comment: 15 pages, 4 figure

Clustering of multiple specific genes and gene-rich R-bands around SC-35 domains: evidence for local euchromatic neighborhoods

Typically, eukaryotic nuclei contain 10–30 prominent domains (referred to here as SC-35 domains) that are concentrated in mRNA metabolic factors. Here, we show that multiple specific genes cluster around a common SC-35 domain, which contains multiple mRNAs. Nonsyntenic genes are capable of associating with a common domain, but domain “choice” appears random, even for two coordinately expressed genes. Active genes widely separated on different chromosome arms associate with the same domain frequently, assorting randomly into the 3–4 subregions of the chromosome periphery that contact a domain. Most importantly, visualization of six individual chromosome bands showed that large genomic segments (∼5 Mb) have striking differences in organization relative to domains. Certain bands showed extensive contact, often aligning with or encircling an SC-35 domain, whereas others did not. All three gene-rich reverse bands showed this more than the gene-poor Giemsa dark bands, and morphometric analyses demonstrated statistically significant differences. Similarly, late-replicating DNA generally avoids SC-35 domains. These findings suggest a functional rationale for gene clustering in chromosomal bands, which relates to nuclear clustering of genes with SC-35 domains. Rather than random reservoirs of splicing factors, or factors accumulated on an individual highly active gene, we propose a model of SC-35 domains as functional centers for a multitude of clustered genes, forming local euchromatic “neighborhoods.