Organization and evolution of C4 and CYP21 genes in primates: importance of genomic segments

The evolutionary relationship between two central major histocompatibility complex (MHC) genes, C4 and CYP21, was investigated by employing pulsed field gel electrophoresis (PFGE) and conventional restriction fragment length polymorphism (RFLP) analyses in human and nonhuman primates. Using Taq I in conjunction with C4 and CYP21 probes, it has been found that there are four major types of C4 genes [defined by 7.0, 6.4, 6.0, and 5.4 kilobases (kb) Taq I fragments] and two major types of CYP21 genes (3.7 and 3.2 kb fragments) in human and nonhuman primates including chimpanzee, gorilla, and orangutan. All of the eight possible combinations of C4 and CYP21 genes can be identified on one or more human ancestral haplotypes (AH). It is concluded that each of the major types of C4 and CYP21 (and each of the combinations between these) predated human speciation. PFGE analysis with Mlu I and Pvu I suggested that each C4 + CYP21 segment has a specific length of 30–50 kb and that each AH carries one, two, three, or even more segments. In the case of C4, it is important to note that there is no simple relationship between the RFLP and the protein classifications. Thus, at least some of the expressed polymorphisms could be relatively recent in that they are carried by the same or different gene types. These findings are consistent with the hypothesis that M MHC AHs have been formed from a large pool of specific genomic segments and that further haplospecific polymorphism has developed subsequently.     

Aerobic scaling and resting metabolism in oviferous and post-spawning Barents Sea capelin Mallotus villosus villosus (Müller, 1776)

As part of the quantitative investigations into the bioenergetic relationships of the Barents Sea capelin, Mallotus villosus villosus (Müller, 1776), resting metabolic rates were examined in the oviferous and post-spawning fish in order to provide insights to aerobic scaling and the basal energetic costs associated with reproduction. Aerobic scaling of the different categories of sexually mature fish (body weight, W=13-54 g) could be expressed as: Q_O2=0.106W^1.049 (oviferous fish; N=11), Q_O2=0.411W^0.430 (post-spawning females; N=9), and Q_O2=0.075W^1.012 (post-spawning males; N=14), where Q_O2 is the oxygen consumption (ml O₂ h⁻¹) per fish. The weight specific oxygen consumption of oviferous capelin was about 30% higher (∼125 ml O₂ kg⁻¹ h⁻¹) compared to those of the post-spawning fish (79-87 ml O₂ kg⁻¹ h⁻¹). The results are discussed in context with other empirical studies on the aerobic scaling and metabolic costs involved with the build-up of roe in the fish.     

Microvillus membrane vesicles from pig small intestine. Purity and lipid composition

Microvillus membrane vesicles from pig small intestine were isolated by a method based on hypotonic lysis, Mg2+-aggregation of contaminants and differential centrifugation. The purity of the membrane vesicles were established by measuring the activity of marker enzymes and the RNA and DNA content. The membranes were found free of contamination by other subcellular membrane fragments, except for a minor contamination with basolateral plasma membranes. The lipid composition was established and, based on weight percentage, the membrane contained neutral lipids, phospholipids, neutral glycolipids and gangliosides in the weight ratio of 18 : 50 : 29 : 2%. The amount of individual phospholipids and glycolipids were quantitated. Phosphatidylethanolamine, -choline, -serine, -inositol and sphingomyelin made up 17, 17, 6, 5 and 5%, respectively of the total lipid. The major glycolipids were two monohexosylceramides containing glucose and galactose as the carbohydrate component, a dihexosylceramide containing galactose as the only carbohydrate component and two pentahexosylceramides containing fucose, galactose, glucose and hexosamine (either N-acetylglucosamine or N-acetylgalactosamine) in the molar ratio of 1 : 2 : 1 : 1.     

The role of the MoFe protein α-125 and β-125 residues in Azotobacter vinelandii MoFe protein–Fe protein interaction

Site-directed mutagenesis and gene-replacement techniques were used to substitute alanine for the MoFe protein α- and β-subunit phenylalanine-125 residues both separately and in combination. These residues are located on the surface of the MoFe protein near the pseudosymmetric axis of symmetry between the α- and β-subunits. Altered MoFe proteins that contain an alanine substitution at only one of the respective positions exhibit proton reduction activities of about 25–50% when compared to that of the wild-type protein. The lower level of proton reduction also corresponds with decreases in the rates of MgATP hydrolysis. The MoFe protein which contains alanine substitutions in both the α- and β- subunits did not exhibit any proton reduction activity or MgATP hydrolysis. Stopped flow spectrophotometry of the singly substituted MoFe proteins indicate primary electron transfer rate constants approximately an order of magnitude slower than what is observed for wild-type MoFe protein, while no primary electron transfer is observed for the doubly substituted MoFe protein. The doubly substituted MoFe protein is able to interact with the Fe protein as shown by chemical crosslinking experiments. However, this protein does not form a tight complex with the Fe protein when treated with MgADP·AlF₄⁻ or when using the altered 127^Δ Fe protein. Stopped flow spectrophotometry was also used to quantitate the first-order dissociation rate constants for the two component proteins. These results suggest that the 125^Phe residues are involved in an early event(s) that occurs upon component protein docking and could be involved in eliciting MgATP hydrolysis.     

On the distinctiveness of the Cape lion (Panthera leo melanochaita Smith, 1842), and a possible new specimen from the Zoological Museum, Copenhagen

The Cape lion was a population of lions that probably inhabited the western part of the Cape Province of South Africa until their extermination by man in the mid-19th century. Only a few skeletal remains are known, making every specimen valuable. In this paper, I report on a possible new male specimen CN1570 from the Zoological Museum in Copenhagen. A multivariate discriminant analysis on 27 craniodental variables provided clear separation between four of the five lion subspecies (Panthera leo krugeri, nubica, persica, senegalensis) that were included, whereas P. l. bleyenberghi showed some overlap with P. l. senegalensis and P. l. krugeri. The only two undisputed Cape lion males grouped separately from all other lions. CN1570 also grouped separately from other lions, and towards the two Cape lions. The external morphology of the Cape lion is often cited as having been different from other sub-Saharan lions, but phenotypic plasticity argues for caution in placing emphasis on mane morphology as a distinguishing character among lion subspecies. Skull morphology, however, appears to clearly distinguish male Cape lions from other African lions.     

Identity of cactus and lettuce spiroplasmas withSpiroplasma citri as determined by DNA-DNA hybridization

The isolation of spiroplasma strains from the cactusOpuntia tuna monstrosa and from aster yellows-diseased lettuce is described. DNA from these strains (ATCC 29594 and ATCC 29747) is compared with DNA fromSpiroplasma citri, and from the corn stunt and suckling mouse cataract spiroplasmas. The cactus and the lettuce isolates are found to be identical withS. citri by this method.     

Uptake studies in adipocytes isolated from rainbow trout (Salmo gairdnerii). A comparison with adipocytes from rat and cat

Adipocytes were isolated from mesenteric adipose tissue of rainbow trout (Salmo gairdnerii) by incubation of tissue slices at 20 degrees C in a buffer containing 3 mg collagenase per ml. These cells were compared to adipocytes from the cat and the rat, isolated by conventional technique (1 mg collagenase per ml buffer, incubation temperature 37 degrees C). Uptake studies of some metabolites were performed with fish, rat and in some cases cat adipocytes. At a glucose concentration of 0.33 mM, the glucose uptake into rat cells was more than twice as fast as in cells from the cat, and more than five times as fast as in trout cells. 2-Amino butyrate resembled glucose in relative uptake rates between species. Metabolite uptake into rat cells was specific, with different uptake rates for different metabolites. The uptake into trout adipocytes proceeded at similar rates for all metabolites tested, provided the concentrations were the same. The uptake rate of glucose into rat cells was stimulated by insulin. Insulin had no effect on glucose uptake into adipocytes from trout.     

Requirements for carotenoids in fish diets

Carotenoids are among the most widespread and important pigment classes in living organisms, and in marine animals, astaxanthin is the most commonly occurring red carotenoid. Carotenoids are vitamin A precursors and are fundamental in photosynthesis and light protection in plants. Increasing attention has been drawn to a possible light protection, cancer prevention and immune enhancement by carotenoids in mammals. Reported functions in fish range from a general enhancement of performance to specific functions in reproduction and metabolism. In this paper, we show that astaxanthin is essential for growth and survival of fish and crawfish, and discuss this fact in relation to the use of purified and semipurified diets in nutritional studies. The similarity in action of astaxanthin and canthaxanthin compared to α-tocopherol (vitamin E) and retinol (vitamin A) suggests that these two carotenoids should be listed among the fat soluble vitamins.