Sensory maps in the olfactory cortex defined by long-range viral tracing of single neurons

Sensory information may be represented in the brain by stereotyped mapping of axonal inputs or by patterning that varies between individuals. In olfaction, a stereotyped map is evident in the first sensory processing centre, the olfactory bulb (OB), where different odours elicit activity in unique combinatorial patterns of spatially invariant glomeruli. Activation of each glomerulus is relayed to higher cortical processing centres by a set of ～20-50 'homotypic' mitral and tufted (MT) neurons. In the cortex, target neurons integrate information from multiple glomeruli to detect distinct features of chemically diverse odours. How this is accomplished remains unclear, perhaps because the cortical mapping of glomerular information by individual MT neurons has not been described. Here we use new viral tracing and three-dimensional brain reconstruction methods to compare the cortical projections of defined sets of MT neurons. We show that the gross-scale organization of the OB is preserved in the patterns of axonal projections to one processing centre yet reordered in another, suggesting that distinct coding strategies may operate in different targets. However, at the level of individual neurons neither glomerular order nor stereotypy is preserved in either region. Rather, homotypic MT neurons from the same glomerulus innervate broad regions that differ between individuals. Strikingly, even in the same animal, MT neurons exhibit extensive diversity in wiring; axons of homotypic MT pairs diverge from each other, emit primary branches at distinct locations and 70-90% of branches of homotypic and heterotypic pairs are non-overlapping. This pronounced reorganization of sensory maps in the cortex offers an anatomic substrate for expanded combinatorial integration of information from spatially distinct glomeruli and predicts an unanticipated role for diversification of otherwise similar output neurons.     

Mutant alpha subunits of Gi2 inhibit cyclic AMP accumulation

One or more of three Gi proteins, Gi1-3, mediates hormonal inhibition of adenylyl cyclase. Whether this inhibition is mediated by the alpha or by the beta gamma subunits of Gi proteins is unclear. Mutations inhibiting the intrinsic GTPase activity of another G protein, the stimulatory regulator of adenylyl cyclase (Gs), constitutively activate it by replacing either of two conserved amino acids in its alpha subunit (alpha s). These mutations create the gsp oncogene which is found in human pituitary and thyroid tumours. In a second group of human endocrine tumours, somatic mutations in the alpha subunit of Gi2 replace a residue cognate to one of those affected by gsp mutations. This implies that the mutations convert the alpha i2 gene into a dominantly acting oncogene, called gip2, and that the mutant alpha i2 subunits are constitutively active. We have therefore assessed cyclic AMP accumulation in cultured cells which stably or transiently express exogenous wild-type alpha i2 complementary DNA or either of two mutant alpha i2 cDNAs. The results show that putatively oncogenic mutations in alpha i2 constitutively activate the protein's ability to inhibit cAMP accumulation.     

Noyesaphytis (Chalcidoidea: Aphelinidae) – an unusual new genus from Madagascar,and a reassessment of Aphelininae classification based on morphology

ABSTRACT

Noyesaphytis Polaszek & Woolley gen. nov. (type species Noyesaphytis lasallei Polaszek & Woolley sp. n. ) is described from Berenty, Tuléar, Madagascar. The genus differs from its closest relatives primarily in the structure of the female antenna, which has a single, elongate flagellum preceded by four anelli, the largest of which could be interpreted as a single anelliform funicle. This type of antenna is unknown in other Aphytini, but approaches the condition found in many Signiphoridae. Noyesaphytis possesses a character state that was until now thought to be an autapomorphy of Azotidae (sole genus Ablerus), being the groove in front of the propodeal spiracle. A second putative autapomorphy shared by Azotidae and Signiphoridae, and also Noyesaphytis, is the presence of anterior projections on the metasomal sterna. However, in Azotidae and Signiphoridae these are narrow, whereas as they are broader in Noyesaphytis. The form of the wing is consistent with Aphytini, although lacking a linea calva. The presumed male of Noyesaphytis lasallei has an antennal structure completely unknown in Aphelinidae, with a 1-segmented clava preceded by an extremely elongate single funicle, and four anelli. Differences between the female and male are discussed, some of which could indicate that the male might eventually be shown to belong to a different species, although the species are undoubtedly congeneric, despite the striking difference in antennal structure which is common in Aphelinidae. The male genitalia also suggest Aphytini. Based on a phylogenetic analysis of 50 morphological characters, we provisionally place Noyesaphytis in Aphytini pending the results of a forthcoming phylogenomic analysis. The new genus is named for its collector, John Noyes (NHM, London), and the new species is named after the late John La Salle.

http://www.zoobank.org/urn:lsid:zoobank.org:pub:6EE6F35C-32A4-4E91-AE39-5E2C173E58BF     

Effects of simulated mountain lion caching on decomposition of ungulate carcasses

Caching of animal remains is common among carnivorous species of all sizes, yet the effects of caching on larger prey are unstudied. We conducted a summer field experiment designed to test the effects of simulated mountain lion ( Puma concolor ) caching on mass loss, relative temperature, and odor dissemination of 9 prey-like carcasses. We deployed all but one of the carcasses in pairs, with one of each pair exposed and the other shaded and shallowly buried (cached). Caching substantially reduced wastage during dry and hot (drought) but not wet and cool (monsoon) periods, and it also reduced temperature and discernable odor to some degree during both seasons. These results are consistent with the hypotheses that caching serves to both reduce competition from arthropods and microbes and reduce odds of detection by larger vertebrates such as bears ( Ursus spp.), wolves ( Canis lupus ), or other lions.     

Role of transposable elements in heterochromatin and epigenetic control

Heterochromatin has been defined as deeply staining chromosomal material that remains condensed in interphase, whereas euchromatin undergoes de-condensation. Heterochromatin is found near centromeres and telomeres, but interstitial sites of heterochromatin (knobs) are common in plant genomes and were first described in maize. These regions are repetitive and late-replicating. In Drosophila, heterochromatin influences gene expression, a heterochromatin phenomenon called position effect variegation. Similarities between position effect variegation in Drosophila and gene silencing in maize mediated by "controlling elements" (that is, transposable elements) led in part to the proposal that heterochromatin is composed of transposable elements, and that such elements scattered throughout the genome might regulate development. Using microarray analysis, we show that heterochromatin in Arabidopsis is determined by transposable elements and related tandem repeats, under the control of the chromatin remodelling ATPase DDM1 (Decrease in DNA Methylation 1). Small interfering RNAs (siRNAs) correspond to these sequences, suggesting a role in guiding DDM1. We also show that transposable elements can regulate genes epigenetically, but only when inserted within or very close to them. This probably accounts for the regulation by DDM1 and the DNA methyltransferase MET1 of the euchromatic, imprinted gene FWA, as its promoter is provided by transposable-element-derived tandem repeats that are associated with siRNAs.     

Mechanism of shape determination in motile cells

The shape of motile cells is determined by many dynamic processes spanning several orders of magnitude in space and time, from local polymerization of actin monomers at subsecond timescales to global, cell-scale geometry that may persist for hours. Understanding the mechanism of shape determination in cells has proved to be extremely challenging due to the numerous components involved and the complexity of their interactions. Here we harness the natural phenotypic variability in a large population of motile epithelial keratocytes from fish (Hypsophrys nicaraguensis) to reveal mechanisms of shape determination. We find that the cells inhabit a low-dimensional, highly correlated spectrum of possible functional states. We further show that a model of actin network treadmilling in an inextensible membrane bag can quantitatively recapitulate this spectrum and predict both cell shape and speed. Our model provides a simple biochemical and biophysical basis for the observed morphology and behaviour of motile cells.