3,859 research outputs found
Phylogeography and allopatric divergence of cypress species (Cupressus L.) in the Qinghai-Tibetan Plateau and adjacent regions
Additional files can be found at http://www.biomedcentral.com/1471-2148/10/194Background Although allopatric speciation is viewed as the most common way in which species originate, allopatric divergence among a group of closely related species has rarely been examined at the population level through phylogeographic analysis. Here we report such a case study on eight putative cypress (Cupressus) species, which each have a mainly allopatric distribution in the Qinghai-Tibetan Plateau (QTP) and adjacent regions. The analysis involved sequencing three plastid DNA fragments (trnD-trnT, trnS-trnG and trnL-trnF) in 371 individuals sampled from populations at 66 localities. Results Both phylogenetic and network analyses showed that most DNA haplotypes recovered or haplotype-clustered lineages resolved were largely species-specific. Across all species, significant phylogeographic structure (NST > GST, P < 0.05) implied a high correlation between haplotypes/lineages and geographic distribution. Two species, C. duclouxiana and C. chengiana, which are distributed in the eastern QTP region, contained more haplotypes and higher diversity than five species with restricted distributions in the western highlands of the QTP. The remaining species, C. funebris, is widely cultivated and contained very little cpDNA diversity. Conclusions It is concluded that the formation of high mountain barriers separating deep valleys in the QTP and adjacent regions caused by various uplifts of the plateau since the early Miocene most likely promoted allopatric divergence in Cupressus by restricting gene flow and fixing local, species-specific haplotypes in geographically isolated populations. The low levels of intraspecific diversity present in most species might stem from population bottlenecks brought about by recurrent periods of unfavorable climate and more recently by the negative impacts of human activities on species' distributions. Our findings shed new light on the importance of geographical isolation caused by the uplift of the QTP on the development of high plant species diversity in the QTP biodiversity hotspot.Publisher PDFPeer reviewe
When tropical and subtropical congeners met:Multiple ancient hybridization events within Eriobotrya were detected in the Yunnan-Guizhou Plateau, a tropical-subtropical transition area in China
Inelastic neutron scattering study of magnetic excitations in SrRuO
Magnetic excitations in \srruo ~ have been studied by inelastic neutron
scattering. The magnetic fluctuations are dominated by incommensurate peaks
related to the Fermi surface nesting of the quasi-one-dimensional - and
-bands. The shape of the incommensurate signal agrees well with RPA
calculations. At the incommensurate {\bf Q}-positions the energy spectrum
considerably softens upon cooling pointing to a close magnetic instability :
\srruo ~does not exhibit quantum criticality but is very close to it. -scaling may be fitted to the data for temperatures above 30 K. Below the
superconducting transition, the magnetic response at the nesting signal is not
found to change in the energy range down to 0.4meV.Comment: 11 pages 9 figure
Experimental Implementaton of Dense Coding Using Nuclear Magnetic Resonance
Quantum dense coding has been demonstrated experimentally in terms of quantum
logic gates and circuits in quantum computation and NMR technique. Two bits of
information have been transmitted through manipulating one of the maximally
entangled two-state quantum pair, which is completely consistent with the
original ideal of Bennett-Wiesner proposal. Although information transmission
happens between spins over inter-atomic distance, the scheme of entanglement
transformation and measurement can be used in other processes of quantum
information and quantum computing.Comment: Some print errors have been corrected, 15 pages, RevTex, 11 figure
High temperature superconductivity (Tc onset at 34K) in the high pressure orthorhombic phase of FeSe
We have studied the structural and superconducting properties of tetragonal
FeSe under pressures up to 26GPa using synchrotron radiation and diamond anvil
cells. The bulk modulus of the tetragonal phase is 28.5(3)GPa, much smaller
than the rest of Fe based superconductors. At 12GPa we observe a phase
transition from the tetragonal to an orthorhombic symmetry. The high pressure
orthorhombic phase has a higher Tc reaching 34K at 22GPa.Comment: 15 pages, 4 figure
Reemerging superconductivity at 48 K across quantum criticality in iron chalcogenides
Pressure plays an essential role in the induction1 and control2,3 of
superconductivity in iron-based superconductors. Substitution of a smaller
rare-earth ion for the bigger one to simulate the pressure effects has
surprisingly raised the superconducting transition temperature Tc to the record
high 55 K in these materials4,5. However, Tc always goes down after passing
through a maximum at some pressure and the superconductivity eventually tends
to disappear at sufficiently high pressures1-3. Here we show that the
superconductivity can reemerge with a much higher Tc after its destruction upon
compression from the ambient-condition value of around 31 K in newly discovered
iron chalcogenide superconductors. We find that in the second superconducting
phase the maximum Tc is as high as 48.7 K for K0.8Fe1.70Se2 and 48 K for
(Tl0.6Rb0.4)Fe1.67Se2, setting the new Tc record in chalcogenide
superconductors. The presence of the second superconducting phase is proposed
to be related to pressure-induced quantum criticality. Our findings point to
the potential route to the further achievement of high-Tc superconductivity in
iron-based and other superconductors.Comment: 20 pages and 7 figure
Cancer-Associated Fibroblasts Neutralize the Anti-tumor Effect of CSF1 Receptor Blockade by Inducing PMN-MDSC Infiltration of Tumors.
Tumor-associated macrophages (TAM) contribute to all aspects of tumor progression. Use of CSF1R inhibitors to target TAM is therapeutically appealing, but has had very limited anti-tumor effects. Here, we have identified the mechanism that limited the effect of CSF1R targeted therapy. We demonstrated that carcinoma-associated fibroblasts (CAF) are major sources of chemokines that recruit granulocytes to tumors. CSF1 produced by tumor cells caused HDAC2-mediated downregulation of granulocyte-specific chemokine expression in CAF, which limited migration of these cells to tumors. Treatment with CSF1R inhibitors disrupted this crosstalk and triggered a profound increase in granulocyte recruitment to tumors. Combining CSF1R inhibitor with a CXCR2 antagonist blocked granulocyte infiltration of tumors and showed strong anti-tumor effects
miRTarBase update 2014: an information resource for experimentally validated miRNA-target interactions
MicroRNAs (miRNAs) are small non-coding RNA molecules capable of negatively regulating gene expression to control many cellular mechanisms. The miRTarBase database (http://mirtarbase.mbc.nctu.edu.tw/) provides the most current and comprehensive information of experimentally validated miRNA-target interactions. The database was launched in 2010 with data sources for >100 published studies in the identification of miRNA targets, molecular networks of miRNA targets and systems biology, and the current release (2013, version 4) includes significant expansions and enhancements over the initial release (2010, version 1). This article reports the current status of and recent improvements to the database, including (i) a 14-fold increase to miRNA-target interaction entries, (ii) a miRNA-target network, (iii) expression profile of miRNA and its target gene, (iv) miRNA target-associated diseases and (v) additional utilities including an upgrade reminder and an error reporting/user feedback system
PIP5KIβ Selectively Modulates Apical Endocytosis in Polarized Renal Epithelial Cells
Localized synthesis of phosphatidylinositol 4,5-bisphosphate [PtdIns(4,5)P2] at clathrin coated pits (CCPs) is crucial for the recruitment of adaptors and other components of the internalization machinery, as well as for regulating actin dynamics during endocytosis. PtdIns(4,5)P2 is synthesized from phosphatidylinositol 4-phosphate by any of three phosphatidylinositol 5-kinase type I (PIP5KI) isoforms (α, β or γ). PIP5KIβ localizes almost exclusively to the apical surface in polarized mouse cortical collecting duct cells, whereas the other isoforms have a less polarized membrane distribution. We therefore investigated the role of PIP5KI isoforms in endocytosis at the apical and basolateral domains. Endocytosis at the apical surface is known to occur more slowly than at the basolateral surface. Apical endocytosis was selectively stimulated by overexpression of PIP5KIβ whereas the other isoforms had no effect on either apical or basolateral internalization. We found no difference in the affinity for PtdIns(4,5)P2-containing liposomes of the PtdIns(4,5)P2 binding domains of epsin and Dab2, consistent with a generic effect of elevated PtdIns(4,5)P2 on apical endocytosis. Additionally, using apical total internal reflection fluorescence imaging and electron microscopy we found that cells overexpressing PIP5KIβ have fewer apical CCPs but more internalized coated structures than control cells, consistent with enhanced maturation of apical CCPs. Together, our results suggest that synthesis of PtdIns(4,5)P2 mediated by PIP5KIβ is rate limiting for apical but not basolateral endocytosis in polarized kidney cells. PtdIns(4,5)P2 may be required to overcome specific structural constraints that limit the efficiency of apical endocytosis. © 2013 Szalinski et al
Association of combination antiretroviral therapy with risk of neurological diseases in patients with HIV/AIDS in Taiwan: a nested case-control study
Heterogeneous neurocognitive impairment remains an important issue, even in the era of combination antiretroviral therapy (cART), with an incidence ranging from 15% to 65%. Although ART drugs with higher penetration scores to the central nervous system (CNS) show better HIV replication control in the CNS, the association between CNS penetration effectiveness (CPE) scores and neurocognitive impairment remains inconclusive. To explore whether ART exposure is associated with the risk of neurological diseases among patients with HIV/AIDS, this study in Taiwan involved 2,571 patients with neurological diseases and 10,284 matched, randomly selected patients without neurological diseases between 2010 and 2017. A conditional logistic regression model was used in this study. The parameters for ART exposure included ART usage, timing of exposure, cumulative defined daily dose (DDD), adherence, and cumulative CPE score. Incident cases of neurological diseases, including CNS infections, cognitive disorders, vasculopathy, and peripheral neuropathy, were obtained from the National Health Insurance Research Database in Taiwan. Odds ratios (ORs) for the risk of neurological diseases were conducted using a multivariate conditional logistic regression model. Patients with a history of past exposure (OR: 1.68, 95% confidence interval [CI]:1.22–2.32), low cumulative DDDs (< 2,500) (OR: 1.28, 95% CI: 1.15–1.42), low adherence (0 < adherence (ADH) ≤ 0.8) (OR: 1.46, 95% CI: 1.30–1.64), or high cumulative CPE scores (>14) (OR: 1.34, 95% CI: 1.14–1.57) had a high risk of neurological diseases. When stratified by classes of ART drugs, patients with low cumulative DDDs or low adherence had a high risk of neurological diseases, including NRTIs, PIs, NNRTIs, INSTIs, and multi-drug tablets. Subgroup analyses also suggested that patients with low cumulative DDDs or low adherence had a high risk of neurological diseases when they had high cumulative CPE scores. Patients with high cumulative DDDs or medication adherence were protected against neurological diseases only when they had low cumulative CPE scores (≤ 14). Patients may be at risk for neurological diseases when they have low cumulative DDDs, low adherence, or usage with high cumulative CPE scores. Continuous usage and low cumulative CPE scores of ART drugs may benefit neurocognitive health in patients with HIV/AIDS
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