Dynactin polices two-way organelle traffic

How is the bidirectional motion of organelles controlled? In this issue, Deacon et al. (2003) reveal the unexpected finding that dynactin (previously known to control dynein-based motility) binds to kinesin II and regulates anterograde movement of Xenopus melanosomes. This result suggests that dynactin may be a key player in coordinating vesicle traffic in this system

Variability of Western Australian isolates of Sclerotinia sclerotiorum and the potential of Local Biological Control Agents

Stem rot disease caused by Sclerotinia sclerotiorum has emerged as a serious problem for canola (Brassica napus L.) production in Western Australia (WA) over the past few years where crop losses can be up to 40% in the worst affected crops. The biological characteristics and pathogenicity of the pathogen in WA is poorly understood. Also the potential for local biological control agents (BCAs) to be used in the management of the disease has not been explored. This paper provides preliminary data in these fields. One hundred and forty isolates of S. sclerotiorum were collected from WA canola growing regions for identification of biological characteristics which include colour of mycelia, growth rate, production of sclerotia, and pathogenicity. Other fungal isolates with potential biological control activity were collected from southern regions of WA. Colour of mycelia of Sclerotinia isolates varied from white, yellowish white, greyish white, brownish white, grey, dark grey to brown. Each isolate had its 24 and 48 hour growth rate recorded after sub-culture on PDA + ampicillin medium. ANOVA showed highly significant differences between growth rates of isolates 24 and 48 hours after being sub-cultured (P≤0.001). There were significant differences in number of sclerotia produced by each isolate. Two potential fungal biological control agents were found in WA, namely isolate KEN1 and isolate MTB1. These local fungal BCAs were found to be effective in inhibiting in vitro both the growth and ability to produce sclerotia of S. sclerotiorum

A tribute to Shinya Inoue and innovation in light microscopy

The 2003 International Prize for Biology was awarded to Shinya Inoue for his pioneering work in visualizing dynamic processes within living cells using the light microscope. He and his scientific descendants are now pushing light microscopy even further by developing new techniques such as imaging single molecules, visualizing processes in living animals, and correlating results from light and electron microscopy

Response of glacier flow and structure to proglacial lake development and climate at Fjallsjökull, south-east Iceland

ABSTRACTOver recent decades, the number of outlet glaciers terminating in lakes in Iceland has increased in line with climate warming. The mass-balance changes of these lake-terminating outlet glaciers are sensitive to rising air temperatures, due to altered glacier dynamics and increased surface melt. This study aims to better understand the relationship between proglacial lake development, climate, glacier dynamics and glacier structure at Fjallsjökull, a large, lake-terminating outlet glacier in south-east Iceland. We used satellite imagery to map glacier terminus position and lake extent between 1973 and 2016, and a combination of aerial and satellite imagery to map the structural architecture of the glacier's terminus in 1982, 1994 and 2011. The temporal evolution of ice surface velocities between 1990 and 2018 was calculated using feature tracking. Statistically significant increases in the rate of terminus retreat and lake expansion were identified in 2001, 2009 and 2011. Our surface velocity and structural datasets revealed the development of localised flow ‘corridors’ over time, which conveyed relatively faster flow towards the glacier's terminus. We attribute the overall changes in dynamics and structural architecture at Fjallsjökull to rising air temperatures, but argue that the spatial complexities are driven by glacier specific factors, such as basal topography.</jats:p

Mucin glycosylation and sulphation in airway epithelial cells is not influenced by cystic fibrosis transmembrane conductance regulator expression

Abnormalities in mucus properties and clearance make a major contribution to the pathology of cystic fibrosis (CF). Our aim was to test the hypothesis that the defects in CF mucus are a direct result of mutations in the CF transmembrane conductance regulator (CFTR) protein. We evaluated a single mucin molecule MUC1F/5ACTR that carries tandem repeat sequence from MUC5AC, a major secreted airway mucin, in a MUC1 mucin vector. To establish whether the presence of mutant or normal CFTR directly influences the O-glycosylation and sulphation of mucins in airway epithelial cells, we used the CFT1-LC3 (DeltaF508 CFTR mutant) and CFT1-LCFSN (wild-type CFTR corrected) human airway epithelial cell lines. MUC1F/5ACTR mucin was immunoprecipitated, centricon purified, and O-glycosylation was evaluated by Matrix-assisted laser desorption ionization and electrospray tandem mass spectrometry to determine the composition of different carbohydrate structures. Mass spectrometry data showed the same O-glycans in both CFTR mutant and wild-type CFTR corrected cells. Metabolic labeling assays were performed to evaluate gross glycosylation and sulphation of the mucins and showed no significant difference in mucin synthesized in six independent clones of these cell lines. Our results show that the absence of functional CFTR protein causes neither an abnormality in mucin O-glycosylation nor an increase in mucin sulphation