Nitrogen acquisition from different spatial distributions by six Great Basin plant species

Plants of different growth form may utilize soil nutrients in various spatial distributions through different scales of foraging. In this study we evaluated the ability of 6 species commonly found in the Great Basin to utilize nitrogen (N) distributed in different patterns. Three growth forms were represented by these 6 species. We applied 15 N-labeled nitrogen in concentrated patches and over broader uniform areas (at approximately 1% the concentration of the patches) in large, outdoor sand-culture plots. Six weeks after N was applied, 2 plants adjacent to the patch (Patch Treatment) and 2 plants within the uniform application (Uniform Treatment) were harvested. One plant 35-45 cm from both applications (Distant Treatment) was also harvested. The proportion of application-derived N in the leaf N pool was calculated and the mass of N this represented was estimated. Winter annual species Aegilops cylindrical and Bromus tectorum utilized the concentrated patches to a greater extent than did perennial species. The mass of N acquired by Patch-Treatment annual plants was significantly greater than by Uniform- and Distant-Treatment plants. Annual plants in the Distant Treatment had very little application-derived N in their leaf tissue. The perennial tussock grasses Agropyron desertorum and Pseudoroegneria spicata differed in utilization of the N applications. Agropyron acquired a greater quantity of N from patches than from uniform applications, and Distant- Treatment plants acquired very little from treatment applications. On the other hand, Pseudoroegneria utilized N in the 3 treatments equally. The shrub species Artemisia tridentata ssp. vaseyana and Chrysothamnus nauseosus also differed in their pattern of N acquisition. There were no differences in quantity of N acquired by plants from different treatments for Chrysothamnus ; all treatment plants acquired appreciable amounts of N from the applications. In contrast, Artemisia tridentata was very effective at acquiring large quantities of N from patches relative to Uniform- and Distant-Treatment plants, and yet there was still appreciable acquisition of applied N by Distant-Treatment Artemisia plants. We compared our results for these species in utilizing N patches with their ability to utilize N pulses (Bilbrough and Caldwell 1997). The annual grasses, Artemisia , and Agropyron were capable of effectively acquiring N from both pulses and patches, whereas Pseudoroegneria was effective in exploiting pulses but not patches. Chrysothamnus was generally not responsive to either patches or pulses. Our results suggest that the 2 shrubs and 2 perennial grasses differed in the scale at which they foraged for nutrients. Some species exhibited a coarse-scale utilization of nutrients while others were clearly capable of fine-scale utilization of spatially distributed nutrient sources. This suggests the potential for at least some spatial niche separation among these species.     

Ovulated oocytes in adult mice derive from non-circulating germ cells

Decades of research in reproductive biology have led to the generally accepted belief that in female mammals, all surviving germ cells enter meiosis at the end of fetal development and as a result, the postnatal ovary harbours a limited supply of oocytes that cannot be replenished or regenerated if lost to injury or disease. However, recent reports have challenged this view, suggesting instead that oocyte production is maintained through continual seeding of the ovary by circulating, bone-marrow-derived germ cells. To test directly the physiological relevance of circulating cells for female fertility, we established transplantation and parabiotic mouse models to assess the capacity of circulating bone marrow cells to generate ovulated oocytes, both in the steady state and after induced damage. Our studies showed no evidence that bone marrow cells, or any other normally circulating cells, contribute to the formation of mature, ovulated oocytes. Instead, cells that travelled to the ovary through the bloodstream exhibited properties characteristic of committed blood leukocytes.     

The influence of early nutrition and environmental rearing on brain growth and behaviour.

Preweaning malnutrition permanently reduced brain size and cellular content but in spite of changes in the adrenocotical stress response no learning deficit was observed. Differential rearing environments did not influence the effects of malnutrition.     

Dynein mutations impair autophagic clearance of aggregate-prone proteins

Mutations that affect the dynein motor machinery are sufficient to cause motor neuron disease. It is not known why there are aggregates or inclusions in affected tissues in mice with such mutations and in most forms of human motor neuron disease. Here we identify a new mechanism of inclusion formation by showing that decreased dynein function impairs autophagic clearance of aggregate-prone proteins. We show that mutations of the dynein machinery enhanced the toxicity of the mutation that causes Huntington disease in fly and mouse models. Furthermore, loss of dynein function resulted in premature aggregate formation by mutant huntingtin and increased levels of the autophagosome marker LC3-II in both cell culture and mouse models, compatible with impaired autophagosome-lysosome fusion.     

Lung cancer: intragenic ERBB2 kinase mutations in tumours

The protein-kinase family is the most frequently mutated gene family found in human cancer and faulty kinase enzymes are being investigated as promising targets for the design of antitumour therapies. We have sequenced the gene encoding the transmembrane protein tyrosine kinase ERBB2 (also known as HER2 or Neu) from 120 primary lung tumours and identified 4% that have mutations within the kinase domain; in the adenocarcinoma subtype of lung cancer, 10% of cases had mutations. ERBB2 inhibitors, which have so far proved to be ineffective in treating lung cancer, should now be clinically re-evaluated in the specific subset of patients with lung cancer whose tumours carry ERBB2 mutations.     

Complex hybrid origin of genetic caste determination in harvester ants

Caste differentiation and division of labour are the hallmarks of insect societies and at the root of their ecological success. Kin selection predicts that caste determination should result from environmentally induced differences in gene expression, a prediction largely supported by empirical data. However, two exceptional cases of genetically determined caste differentiation have recently been found in harvester ants. Here we show that genetic caste determination evolved in these populations after complex hybridization events. We identified four distinct genetic lineages, each consisting of unique blends of the genomes of the parental species, presumably Pogonomyrmex barbatus and P. rugosus. Crosses between lineages H1 and H2 and between J1 and J2 give rise to workers, whereas queens develop from within-lineage matings. Although historical gene flow is evident, genetic exchange among lineages and between lineages and the parental species no longer occurs. This unusual system of caste determination seems to be evolutionarily stable.     

Caenorhabditis elegans early embryogenesis and vulval morphogenesis require chondroitin biosynthesis

Defects in glycosaminoglycan biosynthesis disrupt animal development and can cause human disease. So far much of the focus on glycosaminoglycans has been on heparan sulphate. Mutations in eight squashed vulva (sqv) genes in Caenorhabditis elegans cause defects in cytokinesis during embryogenesis and in vulval morphogenesis during postembryonic development. Seven of the eight sqv genes have been shown to control the biosynthesis of the glycosaminoglycans chondroitin and heparan sulphate. Here we present the molecular identification and characterization of the eighth gene, sqv-5. This gene encodes a bifunctional glycosyltransferase that is probably localized to the Golgi apparatus and is responsible for the biosynthesis of chondroitin but not heparan sulphate. Our findings show that chondroitin is crucial for both cytokinesis and morphogenesis during C. elegans development.