The tailless Ortholog nhr-67 Regulates Patterning of Gene Expression and Morphogenesis in the C. elegans Vulva

Regulation of spatio-temporal gene expression in diverse cell and tissue types is a critical aspect of development. Progression through Caenorhabditis elegans vulval development leads to the generation of seven distinct vulval cell types (vulA, vulB1, vulB2, vulC, vulD, vulE, and vulF), each with its own unique gene expression profile. The mechanisms that establish the precise spatial patterning of these mature cell types are largely unknown. Dissection of the gene regulatory networks involved in vulval patterning and differentiation would help us understand how cells generate a spatially defined pattern of cell fates during organogenesis. We disrupted the activity of 508 transcription factors via RNAi and assayed the expression of ceh-2, a marker for vulB fate during the L4 stage. From this screen, we identified the tailless ortholog nhr-67 as a novel regulator of gene expression in multiple vulval cell types. We find that one way in which nhr-67 maintains cell identity is by restricting inappropriate cell fusion events in specific vulval cells, namely vulE and vulF. nhr-67 exhibits a dynamic expression pattern in the vulval cells and interacts with three other transcriptional regulators cog-1 (Nkx6.1/6.2), lin-11 (LIM), and egl-38 (Pax2/5/8) to generate the composite expression patterns of their downstream targets. We provide evidence that egl-38 regulates gene expression in vulB1, vulC, vulD, vulE, as well as vulF cells. We demonstrate that the pairwise interactions between these regulatory genes are complex and vary among the seven cell types. We also discovered a striking regulatory circuit that affects a subset of the vulval lineages: cog-1 and nhr-67 inhibit both one another and themselves. We postulate that the differential levels and combinatorial patterns of lin-11, cog-1, and nhr-67 expression are a part of a regulatory code for the mature vulval cell types

Current advances in systems and integrative biology

Systems biology has gained a tremendous amount of interest in the last few years. This is partly due to the realization that traditional approaches focusing only on a few molecules at a time cannot describe the impact of aberrant or modulated molecular environments across a whole system. Furthermore, a hypothesis-driven study aims to prove or disprove its postulations, whereas a hypothesis-free systems approach can yield an unbiased and novel testable hypothesis as an end-result. This latter approach foregoes assumptions which predict how a biological system should react to an altered microenvironment within a cellular context, across a tissue or impacting on distant organs. Additionally, re-use of existing data by systematic data mining and re-stratification, one of the cornerstones of integrative systems biology, is also gaining attention. While tremendous efforts using a systems methodology have already yielded excellent results, it is apparent that a lack of suitable analytic tools and purpose-built databases poses a major bottleneck in applying a systematic workflow. This review addresses the current approaches used in systems analysis and obstacles often encountered in large-scale data analysis and integration which tend to go unnoticed, but have a direct impact on the final outcome of a systems approach. Its wide applicability, ranging from basic research, disease descriptors, pharmacological studies, to personalized medicine, makes this emerging approach well suited to address biological and medical questions where conventional methods are not ideal

Global persistence exponent of the double-exchange model

We obtained the global persistence exponent $\theta_g$ for a continuous spin model on the simple cubic lattice with double-exchange interaction by using two different methods. First, we estimated the exponent $\theta_g$ by following the time evolution of probability $P(t)$ that the order parameter of the model does not change its sign up to time $t$ $[P(t)\thicksim t^{-\theta_g}]$. Afterwards, that exponent was estimated through the scaling collapse of the universal function $L^{\theta_g z} P(t)$ for different lattice sizes. Our results for both approaches are in very good agreement each other.Comment: 4 pages, 3 figures, and 3 tables. To appear in Physical Review

Predicting the Impact of Climate Change on Threatened Species in UK Waters

Global climate change is affecting the distribution of marine species and is thought to represent a threat to biodiversity. Previous studies project expansion of species range for some species and local extinction elsewhere under climate change. Such range shifts raise concern for species whose long-term persistence is already threatened by other human disturbances such as fishing. However, few studies have attempted to assess the effects of future climate change on threatened vertebrate marine species using a multi-model approach. There has also been a recent surge of interest in climate change impacts on protected areas. This study applies three species distribution models and two sets of climate model projections to explore the potential impacts of climate change on marine species by 2050. A set of species in the North Sea, including seven threatened and ten major commercial species were used as a case study. Changes in habitat suitability in selected candidate protected areas around the UK under future climatic scenarios were assessed for these species. Moreover, change in the degree of overlap between commercial and threatened species ranges was calculated as a proxy of the potential threat posed by overfishing through bycatch. The ensemble projections suggest northward shifts in species at an average rate of 27 km per decade, resulting in small average changes in range overlap between threatened and commercially exploited species. Furthermore, the adverse consequences of climate change on the habitat suitability of protected areas were projected to be small. Although the models show large variation in the predicted consequences of climate change, the multi-model approach helps identify the potential risk of increased exposure to human stressors of critically endangered species such as common skate (Dipturus batis) and angelshark (Squatina squatina)

Evaluating utilization of beta -blockers as secondary prevention for post myocardial infarction in a Medicaid population

Acute myocardial infarction (AMI) is associated with high mortality and costs to the US healthcare system. Beta-blockers are known to reduce mortality and re-infarction rates when used for long-term prevention following an AMI. They are recommended by the American College of Cardiology (ACC)/American Heart Association (AHA) guidelines in post-AMI patients. However, this therapy is both underused (error of omission in eligible patients) and misused (error of commission in ineligible patients). This study involved two phases. Phase one included evaluating utilization of beta-blockers in a Medicaid population and determining the effect of their utilization on patient outcomes such as mortality, morbidity, utilization of healthcare services and expenditures. Phase two involved determining the association of physician-related factors such as knowledge of contraindications, willingness to prescribe, physician demographics and physician practice characteristics on their beta-blocker prescribing behavior. Phase one of the study revealed 37% inappropriate (misuse and underuse) utilization. During the 12-month follow-up after the incident AMI the appropriately prescribed group had a significantly lower all-cause mortality and lower, but insignificant, cardiac mortality compared to the inappropriately prescribed group. The appropriately prescribed group had significantly higher cardiovascular morbidity and higher utilization in the follow-up period. However, there were indications that the appropriate group was more severely ill as compared to the inappropriate group. Thus, the increase in morbidity and utilization could be due to patient severity rather than appropriate therapy. In phase two, a survey was mailed to 1,019 physicians involved in post-AMI care in WV, of which 261 (25.61%) responded. Physician knowledge of contraindications was not associated with their self-reported beta-blocker prescribing behavior. Physicians\u27 willingness to prescribe was positively associated with their beta-blocker prescribing behavior. Younger age and affiliation with a larger hospital were associated with better beta-blocker prescribing behavior. Multivariate analysis including knowledge, willingness to prescribe, demographics and practice characteristics revealed that willingness to prescribe was the only significant predictor of their beta-blocker prescribing behavior. Findings of this phase indicated a profile of general specialty/family practice physician, older in age, non-university or non-hospital affiliated, and attached to a smaller hospital as the target for interventions to improve beta-blocker prescribing behavior

Bi-Lipschitz geometry of weighted homogeneous surface singularities

We show that a weighted homogeneous complex surface singularity is metrically conical (i.e., bi-Lipschitz equivalent to a metric cone) only if its two lowest weights are equal. We also give an example of a pair of weighted homogeneous complex surface singularities that are topologically equivalent but not bi-Lipschitz equivalent.Comment: 5 pages. Added result that nonhomogeneous cyclic quotients are not conica

Short-time behavior of a classical ferromagnet with double-exchange interaction

We investigate the critical dynamics of a classical ferromagnet on the simple cubic lattice with double-exchange interaction. Estimates for the dynamic critical exponents $z$ and $\theta$ are obtained using short-time Monte Carlo simulations. We also estimate the static critical exponents $\nu$ and $\beta$ studying the behavior of the samples at an early time. Our results are in good agreement with available estimates and support the assertion that this model and the classical Heisenberg model belong to the same universality class