2,375 research outputs found
The coevolution of toxin and antitoxin genes drives the dynamics of bacterial addiction complexes and intragenomic conflict
Bacterial genomes commonly contain âaddictionâ gene complexes that code for both a toxin and a corresponding antitoxin. As long as both genes are expressed, cells carrying the complex can remain healthy. However, loss of the complex (including segregational loss in daughter cells) can entail death of the cell. We develop a theoretical model to explore a number of evolutionary puzzles posed by toxinâantitoxin (TA) population biology. We first extend earlier results demonstrating that TA complexes can spread on plasmids, as an adaptation to plasmid competition in spatially structured environments, and highlight the role of kin selection. We then considered the emergence of TA complexes on plasmids from previously unlinked toxin and antitoxin genes. We find that one of these traits must offer at least initially a direct advantage in some but not all environments encountered by the evolving plasmid population. Finally, our study predicts non-transitive ârock-paper-scissorsâ dynamics to be a feature of intragenomic conflict mediated by TA complexes. Intragenomic conflict could be sufficient to select deleterious genes on chromosomes and helps to explain the previously perplexing observation that many TA genes are found on bacterial chromosomes
Surface Roughness Dominated Pinning Mechanism of Magnetic Vortices in Soft Ferromagnetic Films
Although pinning of domain walls in ferromagnets is ubiquitous, the absence
of an appropriate characterization tool has limited the ability to correlate
the physical and magnetic microstructures of ferromagnetic films with specific
pinning mechanisms. Here, we show that the pinning of a magnetic vortex, the
simplest possible domain structure in soft ferromagnets, is strongly correlated
with surface roughness, and we make a quantitative comparison of the pinning
energy and spatial range in films of various thickness. The results demonstrate
that thickness fluctuations on the lateral length scale of the vortex core
diameter, i.e. an effective roughness at a specific length scale, provides the
dominant pinning mechanism. We argue that this mechanism will be important in
virtually any soft ferromagnetic film.Comment: 4 figure
Contamination in complex healthcare trials:the falls in care homes (FinCH) study experience
BACKGROUND: Trials are at risk of contamination bias which can occur when participants in the control group are inadvertently exposed to the intervention. This is a particular risk in rehabilitation studies where it is easy for trial interventions to be either intentionally or inadvertently adopted in control settings. The Falls in Care Homes (FinCH) trial is used in this paper as an example of a large randomised controlled trial of a complex intervention to explore the potential risks of contamination bias. We outline the FinCH trial design, present the potential risks from contamination bias, and the strategies used in the design of the trial to minimise or mitigate against this. The FinCH trial was a multi-centre randomised controlled trial, with embedded process evaluation, which evaluated whether systematic training in the use of the Guide to Action Tool for Care Homes reduced falls in care home residents. Data were collected from a number of sources to explore contamination in the FinCH trial. Where specific procedures were adopted to reduce risk of, or mitigate against, contamination, this was recorded. Data were collected from study e-mails, meetings with clinicians, research assistant and clinician network communications, and an embedded process evaluation in six intervention care homes. During the FinCH trial, there were six new falls prevention initiatives implemented outside the study which could have contaminated our intervention and findings. Methods used to minimise contamination were: cluster randomisation at the level of care home; engagement with the clinical community to highlight the risks of early adoption; establishing local collaborators in each site familiar with the local context; signing agreements with NHS falls specialists that they would maintain confidentiality regarding details of the intervention; opening additional research sites; and by raising awareness about the importance of contamination in research among participants. CONCLUSION: Complex rehabilitation trials are at risk of contamination bias. The potential for contamination bias in studies can be minimized by strengthening collaboration and dialogue with the clinical community. Researchers should recognise that clinicians may contaminate a study through lack of research expertise
Some Results On Convex Greedy Embedding Conjecture for 3-Connected Planar Graphs
A greedy embedding of a graph into a metric space is a
function such that in the embedding for every pair of
non-adjacent vertices there exists another vertex adjacent
to which is closer to than . This notion of greedy
embedding was defined by Papadimitriou and Ratajczak (Theor. Comput. Sci.
2005), where authors conjectured that every 3-connected planar graph has a
greedy embedding (possibly planar and convex) in the Euclidean plane. Recently,
greedy embedding conjecture has been proved by Leighton and Moitra (FOCS 2008).
However, their algorithm do not result in a drawing that is planar and convex
for all 3-connected planar graph in the Euclidean plane. In this work we
consider the planar convex greedy embedding conjecture and make some progress.
We derive a new characterization of planar convex greedy embedding that given a
3-connected planar graph , an embedding x: V \to \bbbr^2 of is
a planar convex greedy embedding if and only if, in the embedding , weight
of the maximum weight spanning tree () and weight of the minimum weight
spanning tree (\func{MST}) satisfies \WT(T)/\WT(\func{MST}) \leq
(\card{V}-1)^{1 - \delta}, for some .Comment: 19 pages, A short version of this paper has been accepted for
presentation in FCT 2009 - 17th International Symposium on Fundamentals of
Computation Theor
Birth and growth of cavitation bubbles within water under tension confined in a simple synthetic tree
Water under tension, as can be found in several systems including tree
vessels, is metastable. Cavitation can spontaneously occur, nucleating a
bubble. We investigate the dynamics of spon- taneous or triggered cavitation
inside water filled microcavities of a hydrogel. Results show that a stable
bubble is created in only a microsecond timescale, after transient
oscillations. Then, a diffusion driven expansion leads to filling of the
cavity. Analysis reveals that the nucleation of a bubble releases a tension of
several tens of MPa, and a simple model captures the different time scales of
the expansion process
Information Arbitrage in Bipartite Heat Engines
Heat engines and information engines have each historically served as
motivating examples for the development of thermodynamics. While these two
types of systems are typically thought of as two separate kinds of machines,
recent empirical studies of specific systems have hinted at possible
connections between the two. Inspired by molecular machines in the cellular
environment, which in many cases have separate components in contact with
distinct sources of fluctuations, we study bipartite heat engines. We show that
a bipartite heat engine can only produce net output work by acting as an
information engine. Conversely, information engines can only extract more work
than the work consumed to power them if they have access to different sources
of fluctuations, i.e., act as heat engines. We illustrate these findings first
through an analogy to economics and a cyclically controlled 2D ideal gas. We
then explore two analytically tractable model systems in more detail: a
Brownian-gyrator heat engine which we show can be reinterpreted as a
feedback-cooling information engine, and a quantum-dot information engine which
can be reinterpreted as a thermoelectric heat engine. Our results suggest
design principles for both heat engines and information engines at the
nanoscale, and ultimately imply constraints on how free-energy transduction is
carried out in biological molecular machines.Comment: 20 pages, 5 figure
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