Past,present, and future geographic range of the relict Mediterranean and Macaronesian Juniperus phoenicea complex

AimThe aim of this study is to model the past, current, and future distribution of J. phoenicea s.s., J. turbinata, and J. canariensis, based on bioclimatic variables using a maximum entropy model (Maxent) in the Mediterranean and Macaronesian regions.LocationMediterranean and Macaronesian.TaxonCupressaceae, Juniperus.MethodsData on the occurrence of the J. phoenicea complex were obtained from the Global Biodiversity Information Facility (GBIF.org), the literature, herbaria, and the authors’ field notes. Bioclimatic variables were obtained from the WorldClim database and Paleoclim. The climate data related to species localities were used for predictions of niches by implementation of Maxent, and the model was evaluated with ENMeval.ResultsThe potential niches of Juniperus phoenicea during the Last Interglacial period (LIG), Last Glacial Maximum climate (LGM), and Mid‐Holocene (MH) covered 30%, 10%, and almost 100%, respectively, of the current potential niche. Climate warming may reduce potential niches by 30% in RCP2.6 and by 90% in RCP8.5. The potential niches of Juniperus turbinata had a broad circum‐Mediterranean and Canarian distribution during the LIG and the MH; its distribution extended during the LGM when it was found in more areas than at present. The predicted warming in scenarios RCP2.6 and RCP8.5 could reduce the current potential niche by 30% and 50%, respectively. The model did not find suitable niches for J. canariensis during the LIG and the LGM, but during the MH its potential niche was 30% larger than at present. The climate warming scenario RCP2.6 indicates a reduction in the potential niche by 30%, while RCP8.5 so indicates a reduction of almost 60%.Main conclusionsThis research can provide information for increasing the protection of the juniper forest and for counteracting the phenomenon of local extinctions caused by anthropic pressure and climate changes.     

Anatomical and histological structure of the spermoviduct in the ovoviviparous snail Ruthenica filograna (Pulmonata,Clausiliidae)

The spermoviduct is a multifunctional part of the hermaphroditic reproductive system of stylommatophoran pulmonates. In this study, the anatomical and histological features of the spermoviduct in the ovoviviparous Ruthenica filograna are described for the first time. The spermoviduct is composed of three grooves that are not fully separated: the oviductal channel, autospermiduct, and allospermiduct. The wall of each groove is composed of specific subepithelial glandular cells and non-secretory epithelial cells. The prostatic gland is well developed in the proximal part of the spermoviduct and connected to the autospermiduct. In the distal part, the autospermiduct diverges, forming a free vas deferens, while the rest of the spermoviduct becomes a free oviduct. Initially, the free oviduct still contains the allospermiduct and the oviductal channel. Along the spermoviduct is a small diverticulum, that in the proximal section adheres to the allospermiduct, remaining an independent duct, opening into the bursa copulatrix stalk. The reproductive system of R. filograna is similar to those of semitriaulic Stylommatophora, but the allospermiduct, unlike in Helix species, continues in the distal part of the spermoviduct and in the proximal part of the free oviduct.     

Down-Regulation of eIF4GII by miR-520c-3p Represses Diffuse Large B Cell Lymphoma Development

Deregulation of the translational machinery is emerging as a critical contributor to cancer development. The contribution of microRNAs in translational gene control has been established however; the role of microRNAs in disrupting the cap-dependent translation regulation complex has not been previously described. Here, we established that elevated miR-520c-3p represses global translation, cell proliferation and initiates premature senescence in HeLa and DLBCL cells. Moreover, we demonstrate that miR-520c-3p directly targets translation initiation factor, eIF4GII mRNA and negatively regulates eIF4GII protein synthesis. miR-520c-3p overexpression diminishes cells colony formation and reduces tumor growth in a human xenograft mouse model. Consequently, downregulation of eIF4GII by siRNA decreases translation, cell proliferation and ability to form colonies, as well as induces cellular senescence. In vitro and in vivo findings were further validated in patient samples; DLBCL primary cells demonstrated low miR-520c-3p levels with reciprocally up-regulated eIF4GII protein expression. Our results provide evidence that the tumor suppressor effect of miR-520c-3p is mediated through repression of translation while inducing senescence and that eIF4GII is a key effector of this anti-tumor activity.     

Organic nitrogen composition of the tissue culture medium influences Agrobacterium tumefaciens growth and the recovery of transformed Pinus radiata embryonal masses after cocultivation

Repeated attempts to genetically transform Pinus radiata embryonal masses through cocultivation with Agrobacterium tumefaciens on MSG medium were unproductive due to Agrobacterium overgrowth. Timentin at either 200 or 400 mg?l^?1 was ineffective in inhibiting bacterial growth after cocultivation. In this study, the causes of the abundant bacterial growth were investigated by comparing MSG medium with two other media (mLV and DCR) commonly used in conifer somatic embryogenesis. Statistical analysis of the growth data (optical density and number of cell-forming units) showed that bacterium grew significantly more on MSG than on mLV or DCR during the 48-h cocultivation. This enhanced growth was attributed to the higher concentration of L-glutamine in MSG. Lowering the concentration of L-glutamine in MSG to 0.5 g?l^?1 resulted in similar growth of Agrobacterium compared with the other two media. MSG was also superior for the growth of radiata pine cells, with a statistically significant difference after 14 d of culture. Hence, to avoid bacterial overgrowth during and after cocultivation, a two-medium protocol was developed in which cocultivation was carried out on mLV, followed by 5 d on mLV with 400 mg?l^?1 Timentin. Selection for transformed cells and further control of bacterial growth was then performed using MSG with Timentin and Geneticin. By sequential application of these two media, 2,096 cell colonies were selected; of these, 94 were analyzed and 49 were transgenic. These results highlight yet another factor that might be critical for the success of transformation experiments but has not been sufficiently studied until now: the growth dynamics and ability to eliminate A. tumefaciens on various plant tissue culture media.     

Effects of cellular iron deficiency on the formation of vascular endothelial growth factor and angiogenesis.

Background  

Young women diagnosed with breast cancer are known to have a higher mortality rate from the disease than older patients. Specific risk factors leading to this poorer outcome have not been identified. In the present study, we hypothesized that iron deficiency, a common ailment in young women, contributes to the poor outcome by promoting the hypoxia inducible factor-1α (HIF-1α and vascular endothelial growth factor (VEGF) formation. This hypothesis was tested in an in vitro cell culture model system.     

Quality of life in childhood epilepsy with lateralized epileptogenic foci

Background  

Measuring quality of life (QOL) helps to delineate mechanisms underlying the interaction of disease and psychosocial factors. In adults, epileptic foci in the left temporal lobe led to lower QOL and higher depression and anxiety as compared to the right-sided foci. No study addressed the development of QOL disturbances depending on the lateralization of epileptogenic focus. The objective of our study was to examine QOL in children with lateralized epileptiform discharges.