ADOPTION OF SUPPLEMENTAL WORK-AT-HOME: A COMPARATIVE ANALYSIS

The primary purpose of this study is to develop a deeper understanding of the dynamics of the adoption of SWAH. Specifically, it examines how the work and family environments of dual-career male and female and traditional male parents who perform SWAH differ from the work and family environments of their cohorts who do not. People who perform SWAH were found to work significantly more hours per week and more hours at home than those who did not adopt SWAH. The data indicates that men and women who have higher level more challenging jobs (Le., greater work expectations and lower role clarity) were more likely to adopt SWAH than were men and women with fewer career demands. There were no significant differences in the family environments of men who did and did not adopt SWAH. Perceived family responsibility (i.e., family involvement, family expectations) was associated with a woman\u27s tendency to adopt SWAH

Aneuploidy in oocytes is prevented by sustained CDK1 activity through degron masking in cyclin B1

Successful mitosis requires that cyclin B1:CDK1 kinase activity remains high until chromosomes are correctly aligned on the mitotic spindle. It has therefore been unclear why, in mammalian oocyte meiosis, cyclin B1 destruction begins before chromosome alignment is complete. Here, we resolve this paradox and show that mouse oocytes exploit an imbalance in the ratio of cyclin B1 to CDK1 to control CDK1 activity; early cyclin B1 destruction reflects the loss of an excess of non-CDK1-bound cyclin B1 in late prometaphase, while CDK1-bound cyclin B1 is destroyed only during metaphase. The ordered destruction of the two forms of cyclin B1 is brought about by a previously unidentified motif that is accessible in free cyclin B1 but masked when cyclin B1 is in complex with CDK1. This protects the CDK1-bound fraction from destruction in prometaphase, ensuring a period of prolonged CDK1 activity sufficient to achieve optimal chromosome alignment and prevent aneuploidy

Noninvasive Imaging beyond the Diffraction Limit of 3D Dynamics in Thickly Fluorescent Specimens

SummaryOptical imaging of the dynamics of living specimens involves tradeoffs between spatial resolution, temporal resolution, and phototoxicity, made more difficult in three dimensions. Here, however, we report that rapid three-dimensional (3D) dynamics can be studied beyond the diffraction limit in thick or densely fluorescent living specimens over many time points by combining ultrathin planar illumination produced by scanned Bessel beams with super-resolution structured illumination microscopy. We demonstrate in vivo karyotyping of chromosomes during mitosis and identify different dynamics for the actin cytoskeleton at the dorsal and ventral surfaces of fibroblasts. Compared to spinning disk confocal microscopy, we demonstrate substantially reduced photodamage when imaging rapid morphological changes in D. discoideum cells, as well as improved contrast and resolution at depth within developing C. elegans embryos. Bessel beam structured plane illumination thus promises new insights into complex biological phenomena that require 4D subcellular spatiotemporal detail in either a single or multicellular context

Cues and knowledge structures used by mental-health professionals when making risk assessments

Background: Research into mental-health risks has tended to focus on epidemiological approaches and to consider pieces of evidence in isolation. Less is known about the particular factors and their patterns of occurrence that influence clinicians’ risk judgements in practice. Aims: To identify the cues used by clinicians to make risk judgements and to explore how these combine within clinicians’ psychological representations of suicide, self-harm, self-neglect, and harm to others. Method: Content analysis was applied to semi-structured interviews conducted with 46 practitioners from various mental-health disciplines, using mind maps to represent the hierarchical relationships of data and concepts. Results: Strong consensus between experts meant their knowledge could be integrated into a single hierarchical structure for each risk. This revealed contrasting emphases between data and concepts underpinning risks, including: reflection and forethought for suicide; motivation for self-harm; situation and context for harm to others; and current presentation for self-neglect. Conclusions: Analysis of experts’ risk-assessment knowledge identified influential cues and their relationships to risks. It can inform development of valid risk-screening decision support systems that combine actuarial evidence with clinical expertise

Comparative assessment of fluorescent proteins for in vivo imaging in an animal model system.

Fluorescent protein tags are fundamental tools used to visualize gene products and analyze their dynamics in vivo. Recent advances in genome editing have expedited the precise insertion of fluorescent protein tags into the genomes of diverse organisms. These advances expand the potential of in vivo imaging experiments and facilitate experimentation with new, bright, photostable fluorescent proteins. Most quantitative comparisons of the brightness and photostability of different fluorescent proteins have been made in vitro, removed from biological variables that govern their performance in cells or organisms. To address the gap, we quantitatively assessed fluorescent protein properties in vivo in an animal model system. We generated transgenic Caenorhabditis elegans strains expressing green, yellow, or red fluorescent proteins in embryos and imaged embryos expressing different fluorescent proteins under the same conditions for direct comparison. We found that mNeonGreen was not as bright in vivo as predicted based on in vitro data but is a better tag than GFP for specific kinds of experiments, and we report on optimal red fluorescent proteins. These results identify ideal fluorescent proteins for imaging in vivo in C. elegans embryos and suggest good candidate fluorescent proteins to test in other animal model systems for in vivo imaging experiments

A prometaphase mechanism of securin destruction is essential for meiotic progression in mouse oocytes

Securin inhibits the protease separase and must be removed before anaphase to ensure timely chromosome segregation. Here, the authors define a mechanism of securin destruction in prometaphase I in mouse oocytes and demonstrate its importance for successful meiotic progression

Superconducting Phase with Fractional Vortices in the Frustrated Kagome Wire Network at f=1/2

In classical XY kagome antiferromagnets, there can be a novel low temperature phase where $\psi^3=e^{i3\theta}$ has quasi-long-range order but $\psi$ is disordered, as well as more conventional antiferromagnetic phases where $\psi$ is ordered in various possible patterns ($\theta$ is the angle of orientation of the spin). To investigate when these phases exist in a physical system, we study superconducting kagome wire networks in a transverse magnetic field when the magnetic flux through an elementary triangle is a half of a flux quantum. Within Ginzburg-Landau theory, we calculate the helicity moduli of each phase to estimate the Kosterlitz-Thouless (KT) transition temperatures. Then at the KT temperatures, we estimate the barriers to move vortices and effects that lift the large degeneracy in the possible $\psi$ patterns. The effects we have considered are inductive couplings, non-zero wire width, and the order-by-disorder effect due to thermal fluctuations. The first two effects prefer $q=0$ patterns while the last one selects a $\sqrt{3}\times\sqrt{3}$ pattern of supercurrents. Using the parameters of recent experiments, we conclude that at the KT temperature, the non-zero wire width effect dominates, which stabilizes a conventional superconducting phase with a $q=0$ current pattern. However, by adjusting the experimental parameters, for example by bending the wires a little, it appears that the novel $\psi^3$ superconducting phase can instead be stabilized. The barriers to vortex motion are low enough that the system can equilibrate into this phase.Comment: 30 pages including figure