Absorption of glycine and proline from the small intestine of rats infected withEimeria nieschulzi

Summary The absorption of glycine and proline through the jejunum and ileum of rats with anEimeria nieschulzi infection was impaired when the amino acids were presented to the mucosal surface as either a mixture or the dipeptide, glycyl-proline.     

Winter food habits of the pine marten in Colorado

Eighteen pine marten ( Martes americana ) stomachs and 29 intestinal tracts, collected between October 1983 and March 1984 from northern Colorado, were examined for food items. Voles ( Microtus spp.) occurred most frequently, followed by shrews ( Sorex spp.), insects, and vegetative matter.     

Cattail decline at Farmington Bay Waterfowl Management Area

For the last seven years, 1969 to 1976, a steady decline of cattails ( Typha latifolia L.) has been observed at Farmington Bay Waterfowl Management Area, Davis County, Utah. Several parameters of Farmington Bay's environment that could cause or enhance a decline of the marshland vegetation were studied. These parameters included temperature, pH, phenols, oil and grease, heavy metals, fungus pathogens, and salt water intrusion from the Great Salt Lake. Elevated soluble salt concentrations were found to be responsible for the decline. Cattails are weakened or killed when they are exposed to soluble salt concentrations greater than 5.0 gm/liter, and there is a significant (1 percent level) negative correlation ( - 0.68) between soluble salt concentration and cattail height. Symptoms of elevated salt concentrations include stunted growth, leaf tip necrosis (burning), and occasional browning of an entire cattail clone. Furthermore, those salt concentrations that cause physiological stress in cattails also facilitate the growth of a decomposition fungus, Chaetophoma confluens. This fungus causes a rot consisting of irregularly scattered lesions on the surface of the rhizomes and was consistently isolated from rhizomes of declining plants.       

Controls on radial growth of mountain big sagebrush and implications for climate change

Mountain big sagebrush ( Artemisia tridentata Nutt. ssp. vaseyana ) covers large areas in arid regions of western North America. Climate-change models predict a decrease in the range of sagebrush, but few studies have examined details of predicted changes on sagebrush growth and the potential impacts of these changes on the community. We analyzed effects of temperature, precipitation, and snow depth on sagebrush annual ring width for 1969 to 2007 in the Gunnison Basin of Colorado. Temperature at all times of year except winter had negative correlations with ring widths; summer temperature had the strongest negative relationship. Ring widths correlated positively with precipitation in various seasons except summer; winter precipitation had the strongest relationship with growth. Maximum snow depth also correlated positively and strongly with ring width. Multiple regressions showed that summer temperature and either winter precipitation or maximum snow depth, which recharges deeper soil horizons, are both important in controlling growth. Overall, water stress and perhaps especially maximum snow depth appear to limit growth of this species. With predicted increases in temperature and probable reduced snow depth, sagebrush growth rates are likely to decrease. If so, sagebrush populations and cover may decline, which may have substantial effects on community composition and carbon balance.     

Essential role for collectrin in renal amino acid transport

Angiotensin -converting enzyme 2 (ACE2) is a regulator of the renin angiotensin system involved in acute lung failure, cardiovascular functions and severe acute respiratory syndrome (SARS) infections in mammals. A gene encoding a homologue to ACE2, termed collectrin (Tmem27), has been identified in immediate proximity to the ace2 locus. The in vivo function of collectrin was unclear. Here we report that targeted disruption of collectrin in mice results in a severe defect in renal amino acid uptake owing to downregulation of apical amino acid transporters in the kidney. Collectrin associates with multiple apical transporters and defines a novel group of renal amino acid transporters. Expression of collectrin in Xenopus oocytes and Madin-Darby canine kidney (MDCK) cells enhances amino acid transport by the transporter B(0)AT1. These data identify collectrin as a key regulator of renal amino acid uptake.     

Partitioning of oxygen during core formation on the Earth and Mars

Core formation on the Earth and Mars involved the physical separation of metal and silicate, most probably in deep magma oceans. Although core-formation models explain many aspects of mantle geochemistry, they have not accounted for the large differences observed between the compositions of the mantles of the Earth (approximately 8 wt% FeO) and Mars (approximately 18 wt% FeO) or the smaller mass fraction of the martian core. Here we explain these differences as a consequence of the solubility of oxygen in liquid iron-alloy increasing with increasing temperature. We assume that the Earth and Mars both accreted from oxidized chondritic material. In a terrestrial magma ocean, 1,200-2,000 km deep, high temperatures resulted in the extraction of FeO from the silicate magma ocean owing to high solubility of oxygen in the metal. Lower temperatures of a martian magma ocean resulted in little or no extraction of FeO from the mantle, which thus remains FeO-rich. The FeO extracted from the Earth's magma ocean may have contributed to chemical heterogeneities in the lowermost mantle, a FeO-rich D" layer and the light element budget of the core.     

Senataxin, the ortholog of a yeast RNA helicase, is mutant in ataxia-ocular apraxia 2

Ataxia-ocular apraxia 2 (AOA2) was recently identified as a new autosomal recessive ataxia. We have now identified causative mutations in 15 families, which allows us to clinically define this entity by onset between 10 and 22 years, cerebellar atrophy, axonal sensorimotor neuropathy, oculomotor apraxia and elevated alpha-fetoprotein (AFP). Ten of the fifteen mutations cause premature termination of a large DEAxQ-box helicase, the human ortholog of yeast Sen1p, involved in RNA maturation and termination.     

Hot-spot residue in small heat-shock protein 22 causes distal motor neuropathy

Distal hereditary motor neuropathies are pure motor disorders of the peripheral nervous system resulting in severe atrophy and wasting of distal limb muscles. In two pedigrees with distal hereditary motor neuropathy type II linked to chromosome 12q24.3, we identified the same mutation (K141N) in small heat-shock 22-kDa protein 8 (encoded by HSPB8; also called HSP22). We found a second mutation (K141E) in two smaller families. Both mutations target the same amino acid, which is essential to the structural and functional integrity of the small heat-shock protein alphaA-crystallin. This positively charged residue, when mutated in other small heat-shock proteins, results in various human disorders. Coimmunoprecipitation experiments showed greater binding of both HSPB8 mutants to the interacting partner HSPB1. Expression of mutant HSPB8 in cultured cells promoted formation of intracellular aggregates. Our findings provide further evidence that mutations in heat-shock proteins have an important role in neurodegenerative disorders.     

Genetic variation in DLG5 is associated with inflammatory bowel disease

Crohn disease and ulcerative colitis are two subphenotypes of inflammatory bowel disease (IBD), a complex disorder resulting from gene-environment interaction. We refined our previously defined linkage region for IBD on chromosome 10q23 and used positional cloning to identify genetic variants in DLG5 associated with IBD. DLG5 encodes a scaffolding protein involved in the maintenance of epithelial integrity. We identified two distinct haplotypes with a replicable distortion in transmission (P = 0.000023 and P = 0.004 for association with IBD, P = 0.00012 and P = 0.04 for association with Crohn disease). One of the risk-associated DLG5 haplotypes is distinguished from the common haplotype by a nonsynonymous single-nucleotide polymorphism 113G-->A, resulting in the amino acid substitution R30Q in the DUF622 domain of DLG5. This mutation probably impedes scaffolding of DLG5. We stratified the study sample according to the presence of risk-associated CARD15 variants to study potential gene-gene interaction. We found a significant difference in association of the 113A DLG5 variant with Crohn disease in affected individuals carrying the risk-associated CARD15 alleles versus those carrying non-risk-associated CARD15 alleles. This is suggestive of a complex pattern of gene-gene interaction between DLG5 and CARD15, reflecting the complex nature of polygenic diseases. Further functional studies will evaluate the biological significance of DLG5 variants.