Phosphorus retention and transformation in a dammed reservoir of the Thames River, Ontario: Impacts on phosphorus load and speciation

Extensive efforts are underway to reduce phosphorus (P) export from the Lake Erie watershed. On the Canadian side, the Thames River is the largest tributary source of P to Lake Erie’s western basin. However, the role of dams in retaining and modifying riverine P loading to the lake has not been comprehensively evaluated. We assessed whether Fanshawe Reservoir, the largest dam reservoir on the Thames River, acts as a source or sink of P, using year-round discharge and water chemistry data collected in 2018 and 2019. We also determined how in-reservoir processes alter P speciation by comparing the dissolved reactive P to total P ratio (DRP:TP) in upstream and downstream loads. Annually, Fanshawe Reservoir was a net sink for P, retaining 25% (36 tonnes) and 47% (91 tonnes) of TP in 2018 and 2019, respectively. Seasonally, the reservoir oscillated between a source and sink of P. Net P release occurred during the spring of 2018 and the summers of 2018 and 2019, driven by internal P loading and hypolimnetic discharge from the dam. The reservoir did not exert a strong influence on DRP:TP annually, but ratio increases occurred during both summers, concurrent with water column stratification. Our analysis demonstrates that Fanshawe Reservoir is not only an important P sink on the Thames River, but also modulates the timing and speciation of P loads. We therefore propose that the potential of using existing dam reservoirs to attenuate downstream P loads should be more thoroughly explored alongside source based P mitigation strategies.Canada-Ontario Agreement on Great Lakes Water Quality and Ecosystem Health || Canada First Research Excellence Fund through the Lake Futures project of the Global Water Futures

The impact of the metabotropic glutamate receptor and other gene family interaction networks on autism

Although multiple reports show that defective genetic networks underlie the aetiology of autism, few have translated into pharmacotherapeutic opportunities. Since drugs compete with endogenous small molecules for protein binding, many successful drugs target large gene families with multiple drug binding sites. Here we search for defective gene family interaction networks (GFINs) in 6,742 patients with the ASDs relative to 12,544 neurologically normal controls, to find potentially druggable genetic targets. We find significant enrichment of structural defects (P≤2.40E-09, 1.8-fold enrichment) in the metabotropic glutamate receptor (GRM) GFIN, previously observed to impact attention deficit hyperactivity disorder (ADHD) and schizophrenia. Also, the MXD-MYC-MAX network of genes, previously implicated in cancer, is significantly enriched (P≤3.83E-23, 2.5-fold enrichment), as is the calmodulin 1 (CALM1) gene interaction network (P≤4.16E-04, 14.4-fold enrichment), which regulates voltage-independent calcium-activated action potentials at the neuronal synapse. We find that multiple defective gene family interactions underlie autism, presenting new translational opportunities to explore for therapeutic interventions

COADSORBATE INDUCED ORDERING ON Rh(lll) AND Rh(l00) SURFACES: STRUCTURAL AND CHEMICAL EFFECTS

Photograph of pagoda, Toji Temple, Kyoto, JapanPagoda, Toji Temple, Kyoto, Japan

Recombinant viral RdRps can initiate RNA synthesis from circular templates

The crystal structure of the recombinant hepatitis C virus (HCV) RNA-dependent RNA polymerase (RdRp) revealed extensive interactions between the fingers and the thumb subdomains, resulting in a closed conformation with an established template channel that should specifically accept single-stranded templates. We made circularized RNA templates and found that they were efficiently used by the HCV RdRp to synthesize product RNAs that are significantly longer than the template, suggesting that RdRp could exist in an open conformation prior to template binding. RNA synthesis using circular RNA templates had properties similar to those previously documented for linear RNA, including a need for higher GTP concentration for initiation, usage of GTP analogs, sensitivity to salt, and involvement of active-site residues for product formation. Some products were resistant to challenge with the template competitor heparin, indicating that the elongation complexes remain bound to template and are competent for RNA synthesis. Other products were not elongated in the presence of heparin, indicating that the elongation complex was terminated. Lastly, recombinant RdRps from two other flaviviruses and from the Pseudomonas phage φ6 also could use circular RNA templates for RNA-dependent RNA synthesis, although the φ6 RdRp could only use circular RNAs made from the 3′-terminal sequence of the φ6 genome