Hypoxia-inducible factor 1α regulates branching morphogenesis during kidney development

The kidneys are exposed to hypoxic conditions during development. Hypoxia-inducible factor (HIF), an important mediator of the response to hypoxia, is believed to have an important role in development. However, the relationship between HIF and branching morphogenesis has not been elucidated clearly.     

Induction of Multichotomous Branching by CLAVATA Peptide in Marchantia polymorpha

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The branching pattern of major groups of land plants inferred from parsimony analysis of ribosomal RNA sequences

The parsimony and bootstrap branching pattern of major groups of land plants derived from relevant 5S rRNA sequence trees have been discussed in the light of paleobotanical and morphological evidences. Although 5S rRNA sequence information is not useful for dileneating angiosperm relationships, it does capture the earlier phase of land plant evolution. The consensus branching pattern indicates an ancient split of bryophytes and vascular plants from the charophycean algal stem. Among the bryophytes,Marchantia andLophocolea appear to be phylogenetically close and together withPlagiomnium form a monophyletic group.Lycopodium andPsilotum arose early in vascular land plant evolution, independent of fem-sphenopsid branch. Gymnosperms are polyphyletic; conifers, Gnetales and cycads emerge in that order with ginkgo joiningCycas. Among the conifers,Metasequoia,Juniperus andTaxus emerge as a branch independent ofPinus which joins Gnetales. The phylogeny derived from the available ss-RNA sequences shows that angiosperms are monophyletic with monocots and dicots diverging from a common stem. The nucleotide replacements during angiosperm descent from the gymnosperm ancestor which presumably arose around 370 my ago indicates that monocots and dicots diverged around 180 my ago, which is compatible with the reported divergence estimate of around 200 my ago deduced from chloroplast DNA sequences. Since deceased.     

Gait stability,variability and complexity on inclined surfaces

This study evaluated the gait stability, variability, and complexity of healthy young adults on inclined surfaces. A total of 49 individuals walked on a treadmill at their preferred speed for 4 min at inclinations of 6%, 8%, and 10% in upward (UP) and downward (DOWN) conditions, and in horizontal (0%) condition. Gait variability was assessed using average standard deviation trunk acceleration between strides (VAR), gait stability was assessed using margin of stability (MoS) and maximum Lyapunov exponent (λs), and gait complexity was assessed using sample entropy (SEn). Trunk variability (VAR) increased in the medial-lateral (ML), anterior-posterior, and vertical directions for all inclined conditions. The SEn values indicated that movement complexity decreased almost linearly from DOWN to UP conditions, reflecting changes in gait pattern with longer and slower steps as inclination increased. The DOWN conditions were associated with the highest variability and lowest stability in the MoS ML, but not in λs. Stability was lower in UP conditions, which exhibited the largest λs values. The overall results support the hypothesis that inclined surfaces decrease gait stability and alter gait variability, particularly in UP conditions.     

Endoderm development requires centrioles to restrain p53-mediated apoptosis in the absence of ERK activity

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Colony growth responses of the Caribbean octocoral, Pseudopterogorgia elisabethae, to harvesting

Abstract. Colonies of the branching Caribbean gorgonian Pseudopterogorgia elisabethae were subjected to partial mortality at 2 sites in the Bahamas to study how colony growth responds to disturbances such as harvesting, grazing, and storm damage. Colonies were clipped so that either 4 branches or 10 branches remained. Growth rates of branches were then monitored over 1 year and compared with nearby unclipped colonies. No significant differences were found between branch extension rates among the 3 treatments. Extension rates of newly formed branches were significantly greater in all treatments than among branches present at the start of the experiment. Per capita branching rates were greater on the more severely clipped colonies and were smallest on control colonies. The absolute number of branches that became mother branches did not differ among treatments. Colonies clipped so that 4 and 10 branches remained had the same average number of mother branches per colony, and there was no significant difference between treatments in the average number of new branches formed on the colonies. Per capita branching rates were significantly different among treatments only because the relative proportion of branches that became mother branches was higher in colonies with four branches than in treatments with more initial branches. Total growth (cumulative growth on all branches) was not significantly different between the 2 clipped treatments. Many of the control colonies suffered extensive damage, which may have obscured the comparison of clipped and unclipped treatments; however, within the range of these clipping treatments, differing levels of partial mortality did not lead to different recovery rates. The lack of treatment effects is particularly relevant to assessing the effects of harvest techniques on the recovery and productivity of harvested, naturally occurring, colonies.     

Evolutionary rescue by beneficial mutations in environments that change in space and time

A factor that may limit the ability of many populations to adapt to changing conditions is the rate at which beneficial mutations can become established. We study the probability that mutations become established in changing environments by extending the classic theory for branching processes. When environments change in time, under quite general conditions, the establishment probability is approximately twice the ‘effective selection coefficient’, whose value is an average that gives most weight to a mutant''s fitness in the generations immediately after it appears. When fitness varies along a gradient in a continuous habitat, increased dispersal generally decreases the chance a mutation establishes because mutations move out of areas where they are most adapted. When there is a patch of favourable habitat that moves in time, there is a maximum speed of movement above which mutations cannot become established, regardless of when and where they first appear. This critical speed limit, which is proportional to the mutation''s maximum selective advantage, represents an absolute constraint on the potential of locally adapted mutations to contribute to evolutionary rescue.