Blueberry Advisory Committee Research Report

The 1984 edition of the Blueberry Progress Reports was prepared for the Maine Blueberry Commission and the University of Maine Blueberry Advisory Committee by researchers with the Maine Agricultural Experiment Station and Maine Cooperative Extension Service at the University of Maine, Orono. Projects in this report include: 1. Control, biology, and ecology of insects affecting lowbush blueberries . 2. Chemical control of mummyberry disease (Monilinia vaccinii-corymbosi) 3. New Fungicides for control of Botrytis blossom blight 4. Nutritional survey of selected lowbush blueberry fields 5. Interaction of fertility and pruning practices on soil characteristics and lowbush blueberry growth and yield 6. Long term effects of N and NPK fertilizer on plant growth and yield 7. The effect of N fertilization on clonal spread 8. Nutritional responses of the lowbush blueberry in new plantings as related to early establishment 9. The effect of several mulches on frost heaving, soil moisture, soil temperature and rhizome development 10. Effectiveness of mulches and planted lowbush blueberry seedlings for stabilizing soils and increasing plant cover 11. Effect of surface mulches on stabilizing lowbush blueberry soil in barren areas 12. Frequency of fertility application for establishment of lowbush blueberry seedlings 13. Slow release vs liquid fertilizer for establishment of lowbush blueberry seedlings 14. Comparison of rooted cuttings and tissue culture propagated lowbush blueberry plants 15. The effect of growth regulator formulations on growth and rhizome production of the lowbush blueberry 16. Unburned, mowed fields 17. Blueberry concentrate 18. Blueberry product development 19. Dehydrated blueberries 20. Low-calorie blueberry jellies 21. Hexazinone and terbacil mixture for weed control 22. Hexazinone and atrazine mixture for weed control 23. Effect of hexazinone and nitrogen or nitrogen-phosphorus fertilizer on lowbush blueberry plants 24. Hand-wiper applications of herbicides on birch, maple and willow 25. Glyphosate applied after leaf drop for bunchberry control 26. Napropamide for seedling weed control 27. PP333 plant growth regulator 28. Dichlobenil for bunchberry control 29. Effect of hexazinone on weed and blueberry populations 30. Fluazifop-butyl for grass control 31. Hand-wiping and cutting treatments for dogbane 32. Evaluation of airblast sprayer application of asulam for bracken fern control 33. Evaluation of spot treatment of woody weeds with 2,4-D in oil 34. Steam heat as a control of mummyberry diseas

Cavin4b/Murcb Is Required for Skeletal Muscle Development and Function in Zebrafish

Skeletal muscles provide metazoans with the ability to feed, reproduce and avoid predators. In humans, a heterogeneous group of genetic diseases, termed muscular dystrophies ( MD), lead to skeletal muscle dysfunction. Mutations in the gene encoding Caveolin-3, a principal component of the membrane micro-domains known as caveolae, cause defects in muscle maintenance and function; however it remains unclear how caveolae dysfunction underlies MD pathology. The Cavin family of caveolar proteins can form membrane remodeling oligomers and thus may also impact skeletal muscle function. Changes in the distribution and function of Cavin4/Murc, which is predominantly expressed in striated muscles, have been reported to alter caveolae structure through interaction with Caveolin-3. Here, we report the generation and phenotypic analysis of murcb mutant zebrafish, which display impaired swimming capacity, skeletal muscle fibrosis and T-tubule abnormalities during development. To understand the mechanistic importance of Murc loss of function, we assessed Caveolin-1 and 3 localization and found it to be abnormal. We further identified an in vivo function for Murc in Erk signaling. These data link Murc with developmental defects in T-tubule formation and progressive muscle dysfunction, thereby providing a new candidate for the etiology of muscular dystrophy

Tracing fatty acid metabolism by click chemistry.

Fatty acids are abundant constituents of all biological systems, and their metabolism is important for normal function at all levels of an organism. Aberrations in fatty acid metabolism are associated with pathological states and have become a focus of current research, particularly due to the interest in metabolic overload diseases. Here we present a click-chemistry-based method that allows tracing of fatty acid metabolism in virtually any biological system. It combines high sensitivity with excellent linearity and fast sample turnover. Since it is free of radioactivity, it can be combined with any other modern analysis technology and can be used in high-throughput applications. Using the new method, we provide for the first time an analysis of cellular fatty metabolism with high time resolution and a comprehensive comparison of utilization of a broad spectrum of fatty acids in hepatoma and adipose cell lines

Research Resource: A Dual Proteomic Approach Identifies Regulated Islet Proteins During beta-Cell Mass Expansion In Vivo

Diabetes is characterized by insulin insufficiency due to a relative paucity of functional beta-cell mass. Thus, strategies for increasing beta-cell mass in situ are sought-after for therapeutic purposes. Pregnancy is a physiological state capable of inducing robust beta-cell mass expansion, however, the mechanisms driving this expansion are not fully understood. Thus, the aim of this study was to characterize pregnancy-induced changes in the islet proteome at the peak of beta-cell proliferation in mice. Islets from pregnant and nonpregnant littermates were compared via 2 proteomic strategies. In vivo pulsed stable isotope labeling of amino acids in cell culture was used to monitor de novo protein synthesis during the first 14.5 days of pregnancy. In parallel, protein abundance was determined using ex vivo dimethyl labelling at gestational day 14.5. Comparison of the 2 datasets revealed 170 islet proteins to be up regulated as a response to pregnancy. These included several proteins, not previously associated with pregnancy-induced islet expansion, such as CLIC1, STMN1, MCM6, PPIB, NEDD4, and HLTF. Confirming the validity of our approach, we also identified proteins encoded by genes known to be associated with pregnancy-induced islet expansion, such as CHGB, IGFBP5, MATN2, EHHADH, IVD, and BMP1. Bioinformatic analyses demonstrated enrichment and activation of the biological functions: protein synthesis and proliferation, and predicted the transcription factors HNF4 alpha, MYC, MYCN, E2F1, NFE2L2, and HNF1 alpha as upstream regulators of the observed expressional changes. As the first characterization of the islet-proteome during pregnancy, this study provides novel insight into the mechanisms involved in promoting pregnancy-induced beta-cell mass expansion and function