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On the distribution of trace element concentrations in multiple bone elements in 10 Danish medieval and post‐medieval individuals
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S?ren Tullin Anette Sams Jakob Brandt Kirsten Dahl Wei Gong Claus Bekker Jeppesen Thomas Nylandsted Krogh Grith Skytte Olsen Yun Liu Anette Amstrup Pedersen J?rn Meidahl Petersen Bidda Rolin Per-Olof Wahlund Christoph Kalthoff 《PloS one》2012,7(10)
Aims/Hypothesis
Several studies have shown that adiponectin can lower blood glucose in diabetic mice. The aim of this study was to establish an effective adiponectin production process and to evaluate the anti-diabetic potential of the different adiponectin forms in diabetic mice and sand rats.Methods
Human high molecular weight, mouse low molecular weight and mouse plus human globular adiponectin forms were expressed and purified from mammalian cells or yeast. The purified protein was administered at 10–30 mg/kg i.p. b.i.d. to diabetic db/db mice for 2 weeks. Furthermore, high molecular weight human and globular mouse adiponectin batches were administered at 5–15 mg/kg i.p. b.i.d. to diabetic sand rats for 12 days.Results
Surprisingly, none of our batches had any effect on blood glucose, HbA1c, plasma lipids or body weight in diabetic db/db mice or sand rats. In vitro biological, biochemical and biophysical data suggest that the protein was correctly folded and biologically active.Conclusions/Interpretation
Recombinant adiponectin is ineffective at lowering blood glucose in diabetic db/db mice or sand rats. 相似文献5.
M. Skytte Christiansen 《Nordic Journal of Botany》1993,13(3):309-312
The new species, Chalara lichenicola, is characterized by its diminutive, pale brown, 20–47 pm long phialophores arising without any superficial mycelium from the basal parts of the podetium of the lichen Cladonia gracilis as well as from the immature basidiomata of a Tremella sp., likewise parasitic (or saprophytic?) on the same podetia. The phialoconidia are hyaline, unicellular, cylindrical with truncate ends. 2.54.0 × 0.5–0.8 Bunim. It is the first lichenicolous hyphomycete to be included in the form-genus Chalara. 相似文献
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Claudia?M.B. Carvalho Shivakumar Vasanth Marwan Shinawi Chad Russell Melissa?B. Ramocki Chester?W. Brown Jesper Graakjaer Anne-Bine Skytte Angela?M. Vianna-Morgante Ana?C.V. Krepischi Gayle?S. Patel LaDonna Immken Kyrieckos Aleck Cynthia Lim Sau?Wai Cheung Carla Rosenberg Nicholas Katsanis James?R. Lupski 《American journal of human genetics》2014,95(5):565-578
The 17p13.1 microdeletion syndrome is a recently described genomic disorder with a core clinical phenotype of intellectual disability, poor to absent speech, dysmorphic features, and a constellation of more variable clinical features, most prominently microcephaly. We identified five subjects with copy-number variants (CNVs) on 17p13.1 for whom we performed detailed clinical and molecular studies. Breakpoint mapping and retrospective analysis of published cases refined the smallest region of overlap (SRO) for microcephaly to a genomic interval containing nine genes. Dissection of this phenotype in zebrafish embryos revealed a complex genetic architecture: dosage perturbation of four genes (ASGR1, ACADVL, DVL2, and GABARAP) impeded neurodevelopment and decreased dosage of the same loci caused a reduced mitotic index in vitro. Moreover, epistatic analyses in vivo showed that dosage perturbations of discrete gene pairings induce microcephaly. Taken together, these studies support a model in which concomitant dosage perturbation of multiple genes within the CNV drive the microcephaly and possibly other neurodevelopmental phenotypes associated with rearrangements in the 17p13.1 SRO. 相似文献
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Dorthe Mondrup Skytte Jesper Vuust Møller Huizhen Liu Helle Østergren Nielsen Louise Elsa Svenningsen Christina Mernøe Jensen Carl Erik Olsen Søren Brøgger Christensen 《Bioorganic & medicinal chemistry》2010,18(15):5634-5646
Removal of each of the acyl groups of thapsigargin at O-3, O-8 and O-10 significant reduces the affinity of the inhibitors to the SERCA1a pump. Replacement of the acyl groups at O-3 and O-10 with flexible residues could be performed with only a minor decrease of the affinity, whereas introduction of voluminous stiff residues caused dramatic reduction of the affinity. The results can be rationalized on the basis of the interactions of thapsigargin with the SERCA1a pump as revealed from 3D X-ray structural models of thapsigargin bound to the SERCA1a. In conclusion the results confirm and elaborate the previously suggested pharmocophore model of thapsigargin. 相似文献
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Mads Skytte Rasmussen Stéphane Mouilleron Birendra Kumar Shrestha Martina Wirth Rebecca Lee Kenneth Bowitz Larsen 《Autophagy》2017,13(5):834-853
The cysteine protease ATG4B cleaves off one or more C-terminal residues of the inactive proform of proteins of the ortholog and paralog LC3 and GABARAP subfamilies of yeast Atg8 to expose a C-terminal glycine that is conjugated to phosphatidylethanolamine during autophagosome formation. We show that ATG4B contains a C-terminal LC3-interacting region (LIR) motif important for efficient binding to and cleavage of LC3 and GABARAP proteins. We solved the crystal structures of the GABARAPL1-ATG4B C-terminal LIR complex. Analyses of the structures and in vitro binding assays, using specific point mutants, clearly showed that the ATG4B LIR binds via electrostatic-, aromatic HP1 and hydrophobic HP2 pocket interactions. Both these interactions and the catalytic site-substrate interaction contribute to binding between LC3s or GABARAPs and ATG4B. We also reveal an unexpected role for ATG4B in stabilizing the unlipidated forms of GABARAP and GABARAPL1. In mouse embryonic fibroblast (MEF) atg4b knockout cells, GABARAP and GABARAPL1 were unstable and degraded by the proteasome. Strikingly, the LIR motif of ATG4B was required for stabilization of the unlipidated forms of GABARAP and GABARAPL1 in cells. 相似文献
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Michael Riis Hansen Kristine Steen Jensen Mads Skytte Rasmussen Stig Christoffersen Anders Kadziola Kaj Frank Jensen 《Extremophiles : life under extreme conditions》2014,18(1):179-187
Two open reading frames in the genome of Sulfolobus solfataricus (SSO2341 and SSO2424) were cloned and expressed in E. coli. The protein products were purified and their enzymatic activity characterized. Although SSO2341 was annotated as a gene (gpT-1) encoding a 6-oxopurine phosphoribosyltransferase (PRTase), the protein product turned out to be a PRTase highly specific for adenine and we suggest that the reading frame should be renamed apT. The other reading frame SSO2424 (gpT-2) proved to be a true 6-oxopurine PRTase active with hypoxanthine, xanthine and guanine as substrates, and we suggest that the gene should be renamed gpT. Both enzymes exhibited unusual profiles of activity versus pH. The adenine PRTase showed the highest activity at pH 7.5–8.5, but had a distinct peak of activity also at pH 4.5. The 6-oxo PRTase showed maximal activity with hypoxanthine and guanine around pH 4.5, while maximal activity with xanthine was observed at pH 7.5. We discuss likely reasons why SSO2341 in S. solfataricus and similar open reading frames in other Crenarchaeota could not be identified as genes encoding APRTase. 相似文献