Dynamics of phosphoglucomutase heat sensitivity polymorphism in Culicidae

Summary In 6 species of mosquitoes of the generaAedes andCuliseta (Culicidae, Diptera) the frequency of phosphoglucomutase (PGM) heat sensitivity alleles is inversely correlated with the temperature of the environment where larvae develop. These data suggest that different selective values are associated with the PGM thermoresistant and thermosensitive genotypes in the different habitats.We thank Dr M. Coluzzi for providing the data on the temperature ranges for larval development of the species examined and for helpful discussions. The excellent technical assistance of Mr G. Dell'Uomo (Istituto Superiore Sanità, Roma) is also acknowledged.     

Influence of temperature on the sensitivity of adrenergic β-receptors

Zusammenfassung Versuche am Ileum des Kaninchens und der Trachea des Meerschweinchens mit dem Resorcinderivat Orciprenalin⁷ bei 25 bis 42°C führten zu folgenden Ergebnissen: Temperaturerhöhung verminderte am Ileum die Affinität des Orciprenalins, an der Trachea dagegen war sie ohne Einfluss⁸.     

A contribution to the temperature sensitivity of Lorenzinian ampullae of Elasmobranchs

Zusammenfassung In einigen isolierten infraorbitalen Lorenzinischen Ampullen von Katzenhaien wurden Rezeptoren gefunden, deren Erregungsmuster bei Temperatursprüngen dem Verhalten von Warmrezeptoren bei Warmblütern entspricht. Bei einer Reihe von Ampullen, die wie Kaltrezeptoren reagierten, wurde nach Kälteoder Wärmesprüngen ein adaptives Verhalten beobachtet, das von der bisher beschriebenen Reaktionsweise der Lorenzinischen Ampullen bei Temperaturänderungen abweicht.     

Intermediate targets and segmental pathfinding

Neurons must often extend axons over fairly long distances, making multiple changes in their trajectory of growth before arriving at their final target. It has become clear that as growth cones navigate these complex projections, they typically extend toward a number of intermediate targets before they contact their final target. Recent work from a variety of systems has identified intermediate targets that seem to play similar roles in vertebrate and invertebrate nervous system development. From these examples it appears that a general model of axon guidance can be proposed whereby neurons are guided to their targets segmentally. Within each segment, an intermediate target appears to be the primary target for growth cone recognition and thus the completion of the journey to the final target is determined by a series of successful segmental pathfinding decisions.     

Differential sensitivity of pinna reflex and esophageal temperature to clonidine in mice depleted of central noradrenaline by DSP-4

Mice injected with DSP-4 [N-(2-chloroethyl)-N-ethyl-2-bromobenzylamine], a selective noradrenergic neurotoxin, had marked depletions of central noradrenaline and an attenuated post-decapitation reflex. DSP-4-treated mice exhibited an increased sensitivity to the alpha 2-adrenoceptor agonist clonidine as measured by inhibition of the pinna reflex, but normal sensitivity as measured by hypothermia. This differential sensitivity may reflect the presence of supersensitive postsynaptic alpha 2-adrenoceptors in some, but not all, CNS regions after DSP-4 treatment.     

Genetic polymorphism: from electrophoresis to DNA sequences

Summary Recent studies indicate that the amount of protein variation undetected by electrophoresis may be reasonably small. Nevertheless, at the protein level, a typical sexually-reproducing organism may be heterozygous at 20 or more percent of the gene loci. Although the evidence is limited, it appears that at the level of the DNA nucleotide sequence every individual is heterozygous at every locus — if introns as well as exons are taken into account. The evidence available does not support the hypothesis that, at least at the protein level, the variation is adaptively neutral.This work was supported by grant GM 22221 from the PHS (USA).     

TPX2: of spindle assembly,DNA damage response,and cancer

For more than 15 years, TPX2 has been studied as a factor critical for mitosis and spindle assembly. These functions of TPX2 are attributed to its Ran-regulated microtubule-associated protein properties and to its control of the Aurora A kinase. Overexpressed in cancers, TPX2 is being established as marker for the diagnosis and prognosis of malignancies. During interphase, TPX2 resides preferentially in the nucleus where its function had remained elusive until recently. The latest finding that TPX2 plays a role in amplification of the DNA damage response, combined with the characterization of TPX2 knockout mice, open new perspectives to understand the biology of this protein. This review provides an historic overview of the discovery of TPX2 and summarizes its cytoskeletal and signaling roles with relevance to cancer therapies. Finally, the review aims to reconcile discrepancies between the experimental and pathological effects of TPX2 overexpression and advances new roles for compartmentalized TPX2.     

Endocyclic selection and stable polymorphism]

If the period of time from zygotic to adult state is divided in successive intervals where the fitness of a particular genotype takes different values, a stable polymorphism can be maintained in the population, without any superiority of heterozygotes in any interval.     

Aggrecan, aging and assembly in articular cartilage

The primary function of articular cartilage to act as a self-renewing, low frictional material that can distribute load efficiently at joints is critically dependent upon the composition and organisation of the extracellular matrix. Aggrecan is a major component of the extracellular matrix, forming high molecular weight aggregates necessary for the hydration of cartilage and to meet its weight-bearing mechanical demands. Aggregate assembly is a highly ordered process requiring the formation of a ternary complex between aggrecan, link protein and hyaluronan. There is extensive age-associated heterogeneity in the structure and molecular stoichiometry of these components in adult human articular cartilage, resulting in diverse populations of complexes with a range of stabilities that have implications for cartilage mechanobiology and integrity. Recent findings have demonstrated that aggrecan can form ligands with other matrix proteins. These findings provide new insights into mechanisms for aggregate assembly and functional protein networks in different cartilage compartments with maturation and aging.     

Structure and assembly of the 20S proteasome

The barrel-shaped 20S proteasome is one of the two components of a larger 26S particle, the multicatalytic 2000-kDa protease complex. The proteolytic sites are located in the inner chamber of the 20S particle and are only accessible via narrow entrances. This paper reviews the current knowledge concerning proteasome formation, proteolytic activities, structural aspects and assembly. Eukaryotic proteasomes are made up by four rings each of which contains seven different subunits occurring at fixed positions. While the outer rings contain α-type subunits, the inner ones comprise β-type subunits. The current assembly model for eukaryotic 20S proteasomes is based upon the detection of 13S and 16S intermediates, respectively, in addition to previous findings with archaebacterial and eubacterial proteasome assembly. The available data suggest a cooperative assembly of the α-type and β-type subunits into half proteasome-like complexes followed by dimerization into proteasomes. During or after dimerization of half proteasomes, the β-type subunits are processed. The prosequence of the β-type subunits is essential for the assembly process and prevents protease activity of immature proteasomes.     

Scaffolding proteins and their role in viral assembly

Scaffolding proteins are proteins that are required to catalyse, regulate or modulate some step in the assembly of a macromolecular complex. They associate specifically with the nascent protein complex during assembly, but are subsequently removed, and are absent from the mature structure. Scaffolding proteins have been described primarily from viral systems, in particular from the double-stranded DNA bacteriophages, but most likely play a more general role in macromolecular assembly, a fundamental process in all biological systems. Scaffolding proteins may act in a specific fashion, by actively encouraging the formation of correct protein-protein interactions, or more generally by nucleating and promoting assembly. They may also work to ensure the fidelity of the assembly process by preventing the formation of improper interactions, in many ways similar to the role of molecular chaperones in protein folding. In viruses, scaffolding proteins are found both in the form of internal cores and external bracing, and may form elaborate and complex structures. This review will focus on the viral scaffolding proteins, for which an increasing amount of structural and functional information has recently become available.