Contrasting levels of genetic diversity between the historically rare orchid Cypripedium japonicum and the historically common orchid Cypripedium macranthos in South Korea

Many terrestrial orchids are historically rare and occur in small, spatially isolated populations. Theory predicts that such species will harbour low levels of genetic variation within populations and will exhibit a high degree of population genetic divergence, primarily as a result of genetic drift. If the origin of the present‐day populations is relatively recent from the same genetically depauperate source population, a complete lack of genetic differentiation between conspecific populations is expected. If a terrestrial orchid was historically common with moderate or high levels of genetic diversity, but has experienced more recent anthropogenic disturbance as a result of over‐collection, it would still exhibit initial levels of genetic variation within populations and a low degree of genetic divergence between populations. To test these predictions, we examined the genetic diversity in six populations (N = 131) of the historically and currently rare Cypripedium japonicum and in four populations (N = 94) of the historically common but now rare C. macranthos from South Korea. Fourteen putative allozyme loci resolved from eight enzyme systems revealed no variation either within or among populations of C. japonicum, which supports the first prediction. In contrast, populations of C. macranthos harboured high levels of genetic variation (mean percentage of polymorphic loci %P = 46.7; mean expected heterozygosity H_e = 0.185) and exhibited a low degree of population genetic divergence (G_ST = 0.059), supporting the second prediction. The lack of genetic variation both within and among conspecific populations of C. japonicum may suggest that populations originated from the same genetically depauperate ancestral population. The high levels of genetic diversity maintained in populations of C. macranthos suggest that the collection‐mediated decrease in the number of individuals is still too recent for long‐term effects on genetic variation. Based on current demographic and genetic data, in situ and ex situ conservation strategies should be provided to preserve genetic variation and to ensure the long‐term survival of the two species in the Korean Peninsula. © 2009 The Linnean Society of London, Botanical Journal of the Linnean Society, 2009, 160 , 119–129.     

Molecular cloning and expression pattern of 14-3-3ζ from the malaria vector, Anopheles sinensis

14-3-3 proteins are known to play a pivotal role in cell survival, apoptosis and signal transduction. The 14-3-3ζ isoform has been cloned and characterized from many eukaryotic organisms, including the fruit fly and silkworm. However, no study on mosquito 14-3-3 has been reported to date. In an attempt to investigate the function of 14-3-3 in midgut epithelial cells undergoing apoptosis, a cDNA library was generated from the malaria vector, Anopheles sinensis , which was treated with apoptosis-inducing Actinomycin-D. We were able to identify and obtain A. sinensis 14-3-3ζ cDNA ( Ansi14-3-3ζ ) from expressed sequence tags (EST) analysis after conducting massive sequencing of the A. sinensis cDNA library. Ansi14-3-3ζ has very high homology to 14-3-3 homologs of various insects, such as Anopheles gambiae (100%), Aedes aegypti (100%), Drosophila melanogaster (96%), Bombyx mori (93%), Apis mellifera (93%) and Mus musculus (81%), indicating that mosquito 14-3-3ζ is a highly conserved gene in diverse organisms. Analysis of temporal expression patterns showed that Ansi14-3-3ζ mRNA is highly expressed in egg, early pupae and adult stages and is also expressed, although at low levels, in fourth instar larvae and late pupae. In response to two immune elicitors (lipopolysaccharide and laminarin), no striking induction of 14-3-3ζ mRNA was observed in A. sinensis . Further studies of the precise biological function, inducibility and subcellular distribution of 14-3-3ζ are required in Plasmodium invasion-induced apoptotic midgut cells in A. sinensis in the context of the Time Bomb model.     

Juvenile Hormone Binding Protein Titers During Adult Metamorphosis in Manduca sexta

ABSTRACT ABSTRACT During the pupal and adult stages, the JHBP levels displayed a sex-related difference, with females showing higher levels than males. A sharp increase in JHBP levels was observed at day 2 of the pupal stage. After day 2 the JHBP titer declined precipitously, and then remained unchanged until day 12 in males. JHBP titers in females decreased slightly after day 2 and then remained relatively constant until day 12. In both sexes, the JHBP levels showed a steep increase and peaked around day 15. During the previtellogenic period, the JHBP titers declined dramatically until adult ecdysis. During early adult stage, JHBP titiers in the female remained constant at preecdysis level. This information could broaden our understanding of pest physiology during adult metamorphosis, and could have extensive implications for developing insect growth regulators to control agricultural pests.     

Neuronal Cell Death of Abdominal Ganglia (A3) and Characterization of Neuron-Killing Factor in Ventral Nerve Cord from Sweet Potato Hornworm, Agrius convolvuli

ABSTRACT The central nervous system of Agrius convolvuli is composed of brain, followed by subesophageal ganglion, three thoracic ganglia, and eight abdominal ganglia in late larval stage. After metamorphic transition from larva to pupa, thoracic (T₁ and T₂) and abdominal ganglia (A₁ and A₂) are moved toward T₃ and fused together to construct composite ganglion, pterothoracic ganglion. The formation of composite ganglion is completed about 90% at 4 day and 100% at 7 day after pupation. Neuronal cell death was occurred significantly around 3 or 4 day after pupation and just after adult ecdysis. Although 170 neurons were detected 3 day before adult ecdysis, 24 cells were counted 5 day after adult ecdysis. Data of scanning and tandem electron microscope showed the symptom of cell death. In order to identify the mechanism of cell death in A. convolvuli , 1,200 ventral nerve cords were homogenized. Extracts were boiled for 3 minutes at 100°C and collected below 30,000 dalton of molecular mass. Each fraction from reverse phase column chromatography by HPLC system was tested in ventral nerve cord culture system, and fractions having killing activity in culture were isolated. By the addition of 20 hydroxyecdysone, actinomycin D, or cycloheximide into the culture medium, cell death was delayed significantly when compared to control group.     

Mutational analysis of interaction between coat protein and helper component-proteinase of Soybean mosaic virus involved in aphid transmission

Soybean mosaic virus (SMV), a member of the genus Potyvirus , is transmitted by aphids in a non-persistent manner. It has been well documented that the helper component-proteinase (HC-Pro) plays a role as a 'bridge' between virion particles and aphid stylets in the aphid transmission of potyviruses. Several motifs, including the KITC and PTK motifs on HC-Pro and the DAG motif on the coat protein (CP), have been found to be involved in aphid transmission. Previously, we have shown strong interaction between SMV CP and HC-Pro in a yeast two-hybrid system (YTHS). In this report, we further analysed this CP–HC-Pro interaction based on YTHS and an in vivo binding assay to identify crucial amino acid residues for this interaction. Through this genetic approach, we identified two additional amino acid residues (H256 on CP and R455 on HC-Pro), as well as G12 on the DAG motif, crucial for the CP–HC-Pro interaction. We introduced mutations into the identified residues using an SMV infectious clone and showed that these mutations affected the efficiency of aphid transmission of SMV. We also investigated the involvement of the PTK and DAG motifs in the CP–HC-Pro interaction and aphid transmission of SMV. Our results support the concept that physical interaction between CP and HC-Pro is important for potyviral aphid transmission. Based on the combination of our current results with previous findings, the possibility that aphid transmission may be regulated by more complex molecular interactions than the simple involvement of HC-Pro as a bridge is discussed.     

Developmental Exposure to Polychlorinated Biphenyls or Dioxin: Do Changes in Thyroid Function Mediate Effects on Spatial Learning?

Polychlorinated biphenyls (PCBs) and dioxins are widespreadenvironmental contaminants that are suspected of causing cognitivedeficits in children exposed in utero. Very little is knownabout which of the PCB and dioxin congeners present in the environmentare responsible for the changes in cognitive function or aboutthe mechanisms through which these chemicals affect the centralnervous system (CNS). Because both PCBs and dioxins reduce circulatingthyroid hormone levels, it has been proposed that these chemicalsmay affect CNS function indirectly by reducing the availabilityof thyroid hormone to the brain during development. Thyroidhormones play a critical role in brain development, and spatiallearning and memory is one of the behavioral functions mostseverely affected by neonatal hypothyroidism. In the studiesreviewed here, we investigated the effects of three ortho-substitutedPCBs, two coplanar PCBs and 2,3,7,8-tetrachlorodibenzo-p-dioxin(TCDD) on spatial learning and memory in the rat. Pups exposedto PCBs or TCDD in utero and during lactation were tested whenthey reached adulthood. All three ortho-substituted PCBs causeddeficits in spatial learning, but only two of the three reducedcirculating thyroid hormone concentrations. Furthermore, thelearning deficit was observed only in females, but thyroid hormoneswere equally depressed in males and females. Thus, the PCB-induceddeficit in spatial learning did not appear to be mediated bythe decreased thyroid hormone levels. TCDD and coplanar PCBscaused moderate reductions in thyroid hormone, but facilitatedrather than impaired spatial learning, an effect that has beenreported in neonatally hyperthyroid rats. The possibility thatTCDD and coplanar PCBs may act as "mixed" thyroid agonists/antagonistscausing hypothyroid-like effects in some tissues and hyperthyroid-likeeffects in other tissues is discussed.     

A New Species of Theridion Walckenaer (Araneae: Theridiidae) from Korea

A new species, Theridion longipili sp. nov. (Theridiidae), is described from Korea. It is easily distinguished from other congeners by the structure of conductor, radix, median apophysis, and the female epigynum and internal genitalia.     

Peptide-based polyclonal antibody against mosquito 14-3-3ζ recognizes 14-3-3 homolog from dipteran and lepidopteran insects

The 14-3-3 proteins are known to play an important regulatory role in apoptosis, and various cell signaling cascades. However, no investigation on mosquito 14-3-3 has been reported. To investigate the role of 14-3-3 proteins in mosquito midgut cells undergoing apoptosis, we decided to take advantage of Anopheles gambiae genome data, and were able to find Ag14-3-3ζ cDNA and protein sequences from Ensembl ( http://www.ensembl.org ). Further in silico analysis using BLAST search revealed that Ag14-3-3ζ protein is a polypeptide of 248 amino acids, and shares high identity with 14-3-3ζ homologues from Aedes aegypti (100%), Drosophila melanogaster (96%) and Bombyx mori (93%). Due to the perfect match and high homology, we hypothesized that Ag14-3-3ζ peptide antibody may recognize 14-3-3ζ homologs from other anopheline mosquitoes and insects. We thus generated 14-3-3ζ polyclonal antibody against a unique region located in the C-terminal end of Ag14-3-3ζ after in silico epitope analysis. As expected, zoo-western blot analysis of 14-3-3 proteins revealed that a polyclonal antibody against Ag14-3-3ζ peptide recognizes 14-3-3 homologs from dipteran and lepidopteran insects. To our knowledge, this is the first report on polyclonal antibody production against mosquito 14-3-3ζ. The mosquito-based 14-3-3ζ antibody will be very useful for studying the functional characterization of 14-3-3ζ in the context of host–pathogen interactions in midgut and other immune cells.