The Grizzly, October 31, 1986

NCAA Drug Tests Bar All but Natural Highs • History in the Making: U.C. Hosts 1st Big Rock Concert Since Hooters \u2782 • Heefner Organ Pumps New Life Into Founder\u27s Day Rites • Letter: It\u27s All in Your Point of View • Hess Encourages Financial Aid Applicants • Jazzing It Up With Branker • Scope of New Course Broadens Science Offerings • Fear of Mosquitoes and Sex? AIDS Expert Tells What\u27s Next • Akin Follows Losing Teams; Laments Vanished Baseball Dream • C & C to Focus on Scientific and Economic Ideologies • Despite Bad Food and Lack of Beer Freshman Say, We Like It Here. • Grizzlies Clash with Stubborn Mules After Kicking Away at G-burg and \u27Nova • Lady Sticklers Stuck at 8-7 After St. Joe\u27s Loss • Sox Go Home Sans Joy Red Cross(e) Knight Named Series MVP • O\u27Donohue and Haux Power Lady Runners to PAIAW Championship • Ursinus Harries Race to a 5-0 Start • Volleyball\u27s Doleniak Back in Action • Win a VCR. Put Your Foot Where Your Mouth ishttps://digitalcommons.ursinus.edu/grizzlynews/1173/thumbnail.jp

Broad-Scale Non-indigenous Species Monitoring along the West Coast in National Marine Sanctuaries and National Estuarine Research Reserves

Nonindigenous species have caused substantial environmental and economic damage to coastal areas. Moreover, the extent and impacts of nonindigenous species are increasing over time. To develop predictive models and to identify which areas should be targeted for impact mitigation or early detection, we need a basic foundation of knowledge about the spatial and temporal patterns of invasions. This project was developed because we lacked the necessary data to rigorously evaluate the patterns of coastal invasions. This collaborative project, between the Smithsonian Environmental Research Center, the National Estuarine Research Reserve System (NERRS) and the National Marine Sanctuary Program (NMSP), established a rigorous, largescale monitoring and research program for invasive species in nine protected coastal areas along the US West Coast from San Diego, CA, to Kachemak Bay, AK. Our research included two components, broad-scale and site-specific projects. The broad-scale component focused on using standardized protocols to collect data on the composition of fouling communities and nearshore fish and crabs. We collected data from 310 settling plates and 140 traps across nine NERRS Reserves and NMSP Sanctuaries. The four most common taxa on the settling plates were Bryozoa, Tunicata, Cirripedia, and Hydrozoa. We identified these four taxa and also Nudibranchia, a mobile molluscan taxa often associated with fouling organisms, to species and noted which were nonindigenous. We found 132 species in the 5 taxa under study. NIS accounted for over one quarter of the diversity in these taxa, with 31 NIS identified. Over half of tunicate species were non-native. The documented NIS included two new US west coast sitings plus 3 other range extensions. We documented two patterns in NIS, a latitudinal pattern and differences between NIS impacts in marinas versus non-marina sites; research on salinity differences is still underway. Both the number and percent of NIS decreased with increasing latitude. Tijuana River had the most, 21, NIS and Monterey Bay had the highest proportion of NIS (57%). The same pattern of decreasing NIS with increasing latitude was observed when we examined Tunicata only and Bryozoa only. Across latitudes, plates in marinas were more impacted by NIS than were plates in more natural areas. All NIS but one were found at marinas, whereas only half the NIS were found at the non-marina sites. In addition, NIS at marinas accounted for almost 80% of the NIS per site. Therefore, we were able to provide information on the relative risk of invasions for different taxonomic groups and geographic regions. The spatial and habitat patterns can be used for future predictions and will be of even more value once they are confirmed with additional taxonomic groups and hypothesis-driven studies that will continue from this initial study. Our broad-scale trapping study illustrated how recently-introduced NIS quickly can become numerically dominant. Although we only found Carcinus maenas at Elkhorn Slough NERR, this recently introduced nonindigenous crab was very common at this Reserve and was the most abundant crab in our traps at 3 of 7 Elkhorn sites. The site-specific projects were conducted at each Reserve plus Olympic Coast and Monterey Bay Sanctuaries. Several are serving as the first important step in longer term research, such as examining whether a change in shipping policy in Kachemak Bay will increase NIS. Others, such as the South Slough project examining the effect of a salinity cline on the number and proportion of NIS, will be expanded to test hypotheses across several protected areas. Many of these site-specific projects still need further analyses, and analysis is underway

Stabilising normal and mis-sense variant alpha-glucosidase

alpha-Glucosidase (EC 3.2.1.3) is a lysosomal enzyme that hydrolyses alpha-1,4- and alpha-1,6-linkages of glycogen to produce free glucose. A deficiency in alpha-glucosidase activity results in glycogen storage disorder type II (GSD II), also called Pompe disease. Here, d-glucose was shown to be a competitive inhibitor of alpha-glucosidase and when added to culture medium at 6.0 g/L increased the production of this protein by CHO-K1 expression cells and stabilised the enzyme activity. D-Glucose also prevented alpha-glucosidase aggregation/precipitation and increased protein yield in a modified purification scheme. In fibroblast cells, from adult-onset GSD II patients, D-glucose increased the residual level of alpha-glucosidase activity, suggesting that a structural analogue of d-glucose may be used for enzyme enhancement therapy.Kakavanos, Revecca ; Hopwood, John J. ; Lang, Debbie ; Meikle, Peter J. ; Brooks, Doug A

Lysosomal biogenesis in lysosomal storage disorders

Lysosomal biogenesis is an orchestration of the structural and functional elements of the lysosome to form an integrated organelle and involves the synthesis, targeting, functional residence, and turnover of the proteins that comprise the lysosome. We have investigated lysosomal biogenesis during the formation and dissipation of storage vacuoles in two model systems. One involves the formation of sucrosomes in normal skin fibroblasts and the other utilizes storage disorder-affected skin fibroblasts; both of these systems result in an increase in the size and the number of lysosomal vacuoles. Lysosomal proteins, beta-hexosaminidase, alpha-mannosidase, N-acetylgalactosamine-4-sulfatase, acid phosphatase, and the lysosome-associated membrane protein, LAMP-1, were shown to be elevated between 2- and 28-fold above normal during lysosomal storage. Levels of mRNA for the lysosome-associated membrane proteins LAMP-1 and LAMP-2, N-acetylgalactosamine-4-sulfatase, and the 46- and 300-kDa mannose-6-phosphate receptors were also elevated 2- to 8-fold. The up-regulation of protein and mRNA lagged 2-4 days behind the formation of lysosomal storage vacuoles. Correction of storage, in both systems, resulted in the rapid decline of the mRNA to basal levels, with a slower decrease in the levels of lysosomal proteins. Lysosomal biogenesis in storage disorders is shown to be a regulated process which is partially controlled at, or prior to, the level of mRNA. Although lysosomal proteins were differentially regulated, the coordination of these events in lysosomal biogenesis would suggest that a common mechanism(s) may be in operation

Neonatal gene therapy with a gamma retroviral vector in mucopolysaccharidosis VI cats

Mucopolysaccharidosis (MPS) VI is due to a deficiency in the activity of N-acetylgalactosamine 4-sulfatase (4S), also known as arylsulfatase B. Previously, retroviral vector (RV)-mediated neonatal gene therapy reduced the clinical manifestations of MPS I and MPS VII in mice and dogs. However, sulfatases require post-translational modification by sulfatase-modifying factors. MPS VI cats were injected intravenously (i.v.) with a gamma RV-expressing feline 4S, resulting in 5 ± 3 copies of RV per 100 cells in liver. Liver and serum 4S activity were 1,450 ± 1,720 U/mg (26-fold normal) and 107 ± 60 U/ml (13-fold normal), respectively, and were directly proportional to the liver 4S protein levels for individual cats. This study suggests that sulfatase-modifying factor (SUMF) activity in liver was sufficient to result in active enzyme despite overexpression of 4S. RV-treated MPS VI cats achieved higher body weights and longer appendicular skeleton lengths, had reduced articular cartilage erosion, and reduced aortic valve thickening and aortic dilatation compared with untreated MPS VI cats, although cervical vertebral bone lengths were not improved. This demonstrates that therapeutic expression of a functional sulfatase protein can be achieved with neonatal gene therapy using a gamma RV, but some aspects of bone disease remain difficult to treat.Katherine P Ponder, Thomas M O’Malley, Ping Wang, Patricia A O’Donnell, Anne M Traas, Van W Knox, Gustavo A Aguirre, N Matthew Ellinwood, Jason A Metcalf, Bin Wang, Emma J Parkinson-Lawrence, Meg M Sleeper, Doug A Brooks, John J Hopwood and Mark E Haskin