Water balance and fluid consumption in the southern grasshopper mouse, Onychomys torridus

Weight loss was rapid and fluid consumption decreased sharply when Onychomys torridus were exposed to salinities greater than 0.3 Molar. The southern grasshopper mouse is physiologically unspecialized for maintaining water balance in its xeric habitat. The southern grasshopper mouse is capable of weight maintenance on smaller daily water rations than is the northern grasshopper mouse ( Onychomys leucogaster ) . Differences in the water balance of O. torridus and O. leucogaster may influence their local distributions in areas of sympatry.     

Alternative splicing directs the expression of two D2 dopamine receptor isoforms

Dopamine receptors are classified into D1 and D2 subtypes on the basis of their pharmacological properties and the intracellular responses they mediate. The cerebral D2 dopamine receptor is the target of drugs used to alleviate the main symptoms of schizophrenia. Although it is considered to be a single molecular entity, there is evidence that multiple D2-receptor subtypes exist. A complementary DNA encoding a D2 receptor has recently been cloned and the deduced 415-amino-acid sequence indicates that it belongs to the large superfamily of receptors coupled to G proteins, and that its topology consists of seven transmembrane domains. In this family, the genes are frequently without introns and each is believed to encode a unique polypeptide product. Here we show that the gene for the D2 receptor produces two receptor isoforms by alternative messenger RNA splicing, providing a route to receptor diversity in this family. One isoform corresponds to the D2(415) receptor, but the second contains an additional sequence encoding a 29-amino-acid fragment, defining a novel D2(444) receptor isoform. Expression of the two isoforms is tissue-specific, and both are regulated by guanyl nucleotides. As the extra sequence is located within a putative cytoplasmic loop that binds to G proteins, the two isoforms might interact with different G proteins and thereby initiate distinct intracellular signals.     

Loss of the SKI proto-oncogene in individuals affected with 1p36 deletion syndrome is predicted by strain-dependent defects in Ski-/- mice.

Experiments involving overexpression of Ski have suggested that this gene is involved in neural tube development and muscle differentiation. In agreement with these findings, Ski-/- mice display a cranial neural tube defect that results in exencephaly and a marked reduction in skeletal muscle mass. Here we show that the penetrance and expressivity of the phenotype changes when the null mutation is backcrossed into the C57BL6/J background, with the principal change involving a switch from a neural tube defect to midline facial clefting. Other defects, including depressed nasal bridge, eye abnormalities, skeletal muscle defects and digit abnormalities, show increased penetrance in the C57BL6/J background. These phenotypes are interesting because they resemble some of the features observed in individuals diagnosed with 1p36 deletion syndrome, a disorder caused by monosomy of the short arm of human chromosome 1p (refs. 6-9). These similarities prompted us to re-examine the chromosomal location of human SKI and to determine whether SKI is included in the deletions of 1p36. We found that human SKI is located at distal 1p36.3 and is deleted in all of the individuals tested so far who have this syndrome. Thus, SKI may contribute to some of the phenotypes common in 1p36 deletion syndrome, and particularly to facial clefting.     

Human red cells receptors and immune adherence haemagglutination

Résumé Trois types d'hématies humaines sont décrites (fortes, faibles, négatives) selon leur réactivité dans l'adhérence sérologique (agglutination d'hématies humaines, exposées à un couple antigène-anticorps, en présence du complément). Ces différences individuelles sont dues à un récepteur dont la présence sur les hématies positives, est demontrée directement (adsorbtion des réactifs sur les hématies positives) et indirectement (perte de la réactivité par trypsinisation, inhibition de la réaction et préparation de sérums spécifiques anti-récepteur).     

An alternative route for biosynthesis of methylhistamine: In vitro and in vivo formation through decarboxylation ofl-3-methylhistidine

Résumé On a mis en évidence chez le Rat une formation de méthylhistamine-³H par décarboxylation de lal-3-méthylhistidine-³H. Cette réaction se produit in vitro et in vivo dans des tissus riches en histidine décarboxylase et elle est prévenue par un inhibiteur de cette enzyme. Les implications biologiques de l'existence de cette nouvelle voie métabolique sont envisagées.