The genetic control of antibody formation

Studies of the molecular biology of lymphoid cells have markedly increased our understanding of how millions of different antibodies can be synthesized by a single animal. To date, the most detailed understanding has been achieved for the mouse, primarily because of the relatively greater experimental availability of this species. These studies, as well as those involving other species, have shown that the complete genes for antibody polypeptide chains are assembled from disparate genetic elements which are originally widely separated in the genome. The assembly process itself, together with the coding information present in the germ line genetic elements, contributes to the diversity of structure (and thus combining specificities) shown by mature antibody molecules. Specifically, the diversity of structure characteristic of antibody variable regions is due to three distinct mechanisms: innate variability of germ line genes; mismatching of individual gene segments during their somatic rearrangement leading to junctional diversity; and somatic mutation in variable region genetic material during or after the rearrangement. These processes lead to the wide array of combining specificities that permit the humoral immune system of a mature animal to interact with essentially any non-self antigen which it encounters. Complex genetic rearrangements are also responsible for the class switching phenomenon long known to be characteristic of the humoral immune response. A form of homologous recombination between constant region genes, possibly mediated by specific "switching" enzymes, is now believed to be involved in this phenomenon. It is also currently believed that the restriction of gene rearrangement processes to one of the two possible chromosomes of a diploid pair in each cell is responsible for the phenomenon of allelic exclusion that has long been associated with the normal functioning of mammalian B-cells.     

TRANSLOCATION OF AMINOTRIAZOLE AND DALAPON IN AG ROPY RON REPENS (L.) BEAUV.

Summary. Tracer studies using single drops of solutions containing 3–amino-1,2,4–triazole-5–¹⁴C (aminotriazole-¹⁴C) or 2,2–dichloropropionic acid-2–¹⁴C (datapon-¹⁴C) revealed that in couch plants (Agropyron repens (L.) Beauv.) growing under field conditions in the autumn and at the stage where the aerial shoots were 40–50 cm long, both compounds moved in both symplast and apoplast. Dalapon was less mobile in the symplast than aminotriazole and only negligible amounts of dalapon were translocated to the rhizomes. The nodes of the treated shoots appeared to act as barriers to translocation, a phenomenon more pronounced for dalapon than for aminotriazole.
Application to a basal green leaf led to a more uniform distribution of the compounds within plants and rhizomes than when the application was made to the youngest fully-expanded leaf.
In couch plants with aerial shoots 10–15 cm long treated in the stubble, the distribution of both aminotriazole and dalapon was mainly restricted to the treated shoots. Even 15 days after application only trace amounts of radioactivity could be found in the rhizomes and untreated shoots.     

A survey of the phosphorus and calcium contents of pastures and the serum inorganic phosphorus and calcium contents of cows on four Manawatu dairy farms

Serum inorganic phosphorus (Pi) and calcium (Ca) concentrations were assessed in 20 cows on each of four Manawatu factory supply dairy farms. Blood was taken from each cow before calving and at six-week intervals during lactation. Bleeding coincided with herd testing. Herds of Friesian or Friesian X cows and Jersey or Jersey X cows were compared on adjacent farms on a Central Yellow-brown Sand and on adjacent farms on a Peat Loam overlying a Central Yellow-brown Earth soil. Pasture mass and composition were estimated to grazing height in the next two paddocks to be grazed in the rotation. Mean serum Pi concentration was higher in cows on sandy soils (1.55 mmol Pi/l than in cows on the peat loam (1.34 mmol Pi/l (P<0.001). Concentrations were highest before calving (1.69 mmol Pi/l) but fell to low levels at peak lactation (1.17mmol Pi/l when 70% of cows were below the minima of the 'normal range', and during the drought (1.29 mmol Pi/l. Pasture phosphorus (P) concentrations were adequate to support cow nutrition for lactation (>0.33% DM, ad lib. feeding) until the summer drought when low herbage mass would have restricted milk production. Serum Ca was adequate for lactating cows and changed little between months or between cows (mean 2.12 mmol Ca/l). No metabolic disorders relating to mineral deficiencies were observed. It appears that serum Pi in a high proportion of cows falls below the normal range during peak lactation without cows displaying clinical deficiency symptoms or a depression in butterfat production.