The pch2Δ Mutation in Baker's Yeast Alters Meiotic Crossover Levels and Confers a Defect in Crossover Interference

Pch2 is a widely conserved protein that is required in baker's yeast for the organization of meiotic chromosome axes into specific domains. We provide four lines of evidence suggesting that it regulates the formation and distribution of crossover events required to promote chromosome segregation at Meiosis I. First, pch2Δ mutants display wild-type crossover levels on a small (III) chromosome, but increased levels on larger (VII, VIII, XV) chromosomes. Second, pch2Δ mutants show defects in crossover interference. Third, crossovers observed in pch2Δ require both Msh4-Msh5 and Mms4-Mus81 functions. Lastly, the pch2Δ mutation decreases spore viability and disrupts crossover interference in spo11 hypomorph strains that have reduced levels of meiosis-induced double-strand breaks. Based on these and previous observations, we propose a model in which Pch2 functions at an early step in crossover control to ensure that every homolog pair receives an obligate crossover

The dissociation of interleukin-2 production and antigen-specific helper activity by clonal analysis.

Influenza virus immune human T-lymphocyte clones maintained in continuous culture in TCGF were analysed for helper activity and interleukin-2 (IL-2) production. The clones that functioned as helper cells in the production of specific antibody failed to release detectable amounts of IL-2. Conversely, the T cells that produced IL-2 were unable to provide either specific or non-specific helper function. These findings indicated the IL-2 is not an essential component for helper activity. However, phenotypic analysis revealed that both the functional subsets of T-cell clones expressed the helper phenotype in that they were T4+, T3+ and T11+. Nevertheless analysis with other antibodies revealed differences in that the IL-2 releasing clone showed greater staining with the anti-T-cell subset antibodies 9.3 and Leu 8, confirming that there is phenotype as well as functional heterogeneity within the helper inducer T-cell population

Fertiliser contaminants in New Zealand grazed pasture with special reference to cadmium and fluorine: a review

Phosphorus (P) fertilisers are an essential input for the economic production of legume-based pastures in New Zealand (NZ) and Australia, but they often contain some unwanted elements that can contaminate the soil, thereby creating potential risks to the health of grazing animal, food quality, and soil quality. Fluorine (F) and cadmium (Cd) are considered to be the elements of most concern. Incidences of F toxicity (from direct ingestion of fertiliser), and accumulation of Cd in offal products above the maximum permissible concentration (MPC) set by the food authorities, have been reported in NZ. Similarly, Cd concentrations in some food grains may exceed the newly proposed MPCs by the Australian and New Zealand Food Authority. Cadmium and F continue to accumulate in the topsoils of NZ and Australian pastures as a result of P fertiliser use. The mobility of both these elements in soils is low and is similar to that of P. Risk of ground water contamination from F and Cd applied to most NZ pastures is low. The plant uptake of these elements, especially F, is also low in most pastoral soils. Cadmium accumulates mainly in liver and kidney of grazing animals mostly through herbage ingestion, whereas F accumulates mainly in the bones of these animals, mostly through soil ingestion. Soil ingestion is highest during the wetter winter months and at high stocking rates. Models have been developed to assess the impact of fertiliser use on the potential risks associated with F and Cd accumulation in soils. Measures to control F and Cd accumulation in soils, plants, and grazing animals are presented and future research needs are identified

The dissociation of interleukin-2 production and antigen-specific helper activity by clonal analysis.

Influenza virus immune human T-lymphocyte clones maintained in continuous culture in TCGF were analysed for helper activity and interleukin-2 (IL-2) production. The clones that functioned as helper cells in the production of specific antibody failed to release detectable amounts of IL-2. Conversely, the T cells that produced IL-2 were unable to provide either specific or non-specific helper function. These findings indicated the IL-2 is not an essential component for helper activity. However, phenotypic analysis revealed that both the functional subsets of T-cell clones expressed the helper phenotype in that they were T4+, T3+ and T11+. Nevertheless analysis with other antibodies revealed differences in that the IL-2 releasing clone showed greater staining with the anti-T-cell subset antibodies 9.3 and Leu 8, confirming that there is phenotype as well as functional heterogeneity within the helper inducer T-cell population