Nucleic Acid Conformation: Crystal Structure of a Naturally Occurring Dinucleoside Phosphate (UpA)

THEORIES of the molecular structure of nucleic acids have so far been based on evidence from the crystal structures of monomeric units such as nucleosides and mononucleotides, the interpretation of diffraction patterns of oriented nucleic acid fibres and molecular model building^1–6. Such approaches can help to suggest structures of periodic molecules such as helices, but they are insufficient for predicting and understanding nonrepetitive structures such as the loops in transfer RNA (tRNA), presumably associated with many of the functions of tRNA. To understand the geometry of nucleic acids and possible constraints on their conformation, it is therefore essential to know the detailed conformation of the sugar residues and the conformational relationship between the sugar residue, the base and the phosphate group^7–9. The simplest molecule which contains this information is a 3´5´-dinucleoside phosphate. We now report the structure of uridine-3´,5´-adenosine phosphate (UpA). This is the first naturally occurring dinucleoside phosphate whose crystal structure has been determined by X-ray diffraction. The only other dinucleoside phosphate with known crystal structure is adenosine-2´,5´-uridine phosphate¹⁰, but it does not have the naturally occurring 3´5´ sugar phosphate linkage.     

All Lipid-soluble Anaesthetics protect Red Cells

FOR the study of molecular events involved in the membrane action of anaesthetics, a cell is required which responds to all anaesthetics and which has a membrane that can be readily isolated. Erythrocytes may serve this purpose both qualitatively and quantitatively, for all lipid-soluble anaesthetics examined so far protect these cells from hypotonic haemolysis. Table 1 lists the anti-haemolytic concentrations of twelve different families of lipid-soluble anaesthetics including steroids¹, alcohols^2,3, tranquillizers⁴, fatty acids⁵, detergents^6,7, propranolol⁸, vasodilators⁹ and barbiturates¹⁰. Drugs which are highly water-soluble, on the other hand, do not protect erythrocytes from hypotonic haemolysis. Tetrodotoxin is a lipid-insoluble local anaesthetic and does not protect human erythrocytes; this compound, however, does not always anaesthetize excitable membranes¹⁸.     

Influence of experimental warming and shading on host–parasitoid synchrony

As the climate warms, many species are showing altered phenology patterns, potentially disrupting synchrony between interacting species. Recent studies have documented disrupted synchrony in plant–herbivore and predator–prey interactions. However, studies investigating climate‐related asynchrony in host–parasitoid interactions and exploring the relative responses of interacting hosts and parasitoids to climate change are lacking. This is an important gap in knowledge given the ubiquity of insect parasitoids and their importance in influencing the abundance and dynamics of their hosts. In the threatened marsh fritillary butterfly Euphydryas aurinia (Lepidoptera: Nymphalidae) and its specialized parasitoid, Cotesia bignellii (Hymenoptera: Braconidae) phenological synchrony (and consequently population fluctuations) are thought to be weather‐dependent. To assess the likely influence of climate and microenvironment change on synchrony between E. aurinia and C. bignellii, we experimentally manipulated the exposure of sensitive‐stage host larvae and parasitoid pupae to temperature (ambient or elevated) and shading (shaded or unshaded) regimes. We also analysed a 20‐year population dynamic dataset from the United Kingdom for E. aurinia to investigate whether population variations could be explained by interannual variations in the thermal and sunshine environment. Development times were affected significantly by the experimental temperature and shading treatments for E. aurinia but not for C. bignellii. However, the contrasting responses were insufficient to significantly affect host availability for parasitoids. In the field, thermal and sunshine conditions did not influence population fluctuations, and population variations across a large (UK‐wide) scale were uncorrelated. Changes to the thermal and sunshine environment of the magnitude investigated in our experiment and within the range experienced by wild E. aurinia populations over the last 20‐years thus seem unlikely to cause breakdown in host–parasitoid synchrony. We suggest that experiments investigating the mechanistic responses of interacting species to environmental change are needed to support the analysis and interpretation of observational data on species' phenology.