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81.
Evolution of Mycobacterium ulcerans and other mycolactone-producing mycobacteria from a common Mycobacterium marinum progenitor 下载免费PDF全文
Yip MJ Porter JL Fyfe JA Lavender CJ Portaels F Rhodes M Kator H Colorni A Jenkin GA Stinear T 《Journal of bacteriology》2007,189(5):2021-2029
It had been assumed that production of the cytotoxic polyketide mycolactone was strictly associated with Mycobacterium ulcerans, the causative agent of Buruli ulcer. However, a recent study has uncovered a broader distribution of mycolactone-producing mycobacteria (MPM) that includes mycobacteria cultured from diseased fish and frogs in the United States and from diseased fish in the Red and Mediterranean Seas. All of these mycobacteria contain versions of the M. ulcerans pMUM plasmid, produce mycolactones, and show a high degree of genetic relatedness to both M. ulcerans and Mycobacterium marinum. Here, we show by multiple genetic methods, including multilocus sequence analysis and DNA-DNA hybridization, that all MPM have evolved from a common M. marinum progenitor to form a genetically cohesive group among a more diverse assemblage of M. marinum strains. Like M. ulcerans, the fish and frog MPM show multiple copies of the insertion sequence IS2404. Comparisons of pMUM and chromosomal gene sequences demonstrate that plasmid acquisition and the subsequent ability to produce mycolactone were probably the key drivers of speciation. Ongoing evolution among MPM has since produced at least two genetically distinct ecotypes that can be broadly divided into those typically causing disease in ectotherms (but also having a high zoonotic potential) and those causing disease in endotherms, such as humans. 相似文献
82.
Protein kinase B/Akt prevents fatty acid-induced apoptosis in pancreatic beta-cells (INS-1) 总被引:30,自引:0,他引:30
Wrede CE Dickson LM Lingohr MK Briaud I Rhodes CJ 《The Journal of biological chemistry》2002,277(51):49676-49684
83.
McArdle F Rhodes LE Parslew R Jack CI Friedmann PS Jackson MJ 《Free radical biology & medicine》2002,33(10):1355-1362
Previous studies of cultured skin cells and murine skin in vivo have indicated that UVR-induced damage involves the generation of reactive oxygen species and depletion of endogenous antioxidant systems. In order to explore the relevance of this to UVR-induced damage to human skin, we have undertaken a detailed examination of the time-course of changes in markers of oxidative stress in human skin following exposure to physiological amounts of UVR in vivo. In addition, we have examined the skin bioavailability of a common nutritional antioxidant, vitamin C, and have assessed the effects of supplementation on markers of oxidative stress. Our hypothesis was that acute exposure of human skin to UVR in vivo would lead to oxidation of cellular biomolecules that could be prevented by prior vitamin C treatment. A UVR-challenge of 120 mJ/cm2 of broadband UVB (peak 310 nm, range 270-400 nm) was applied to buttock skin of 8 healthy volunteers. This caused a rapid and significant rise in activity of skin catalase at 1 h and an increase in the oxidized/total glutathione ratio at 6 h post-UVR. AP-1 DNA binding also peaked at 1-6 h post-UVR, then declined rapidly to baseline levels. No significant changes were seen in skin malonaldehyde content. Oral vitamin C supplements (500 mg/day) were taken by 12 volunteers for 8 weeks resulting in significant rises in plasma and skin vitamin C content. Supplementation had no effect on the UVR-induced erythemal response. The skin malonaldehyde content was reduced by vitamin C supplementation, but surprisingly, reductions in the skin content of total glutathione and protein thiols were also seen. We speculate that this apparently paradoxical effect could be due to regulation of total reductant capacity by skin cells, such that vitamin C may have been replacing other reductants in these cells. No evidence was obtained for an effect of the supplementary vitamin C on the mild oxidative stress seen in human skin following UVR exposure. 相似文献
84.
Ylenia Chiari Chaz Hyseni Tom H. Fritts Scott Glaberman Cruz Marquez James P. Gibbs Julien Claude Adalgisa Caccone 《PloS one》2009,4(7)
Galápagos tortoises represent the only surviving lineage of giant tortoises that exhibit two different types of shell morphology. The taxonomy of Galápagos tortoises was initially based mainly on diagnostic morphological characters of the shell, but has been clarified by molecular studies indicating that most islands harbor monophyletic lineages, with the exception of Isabela and Santa Cruz. On Santa Cruz there is strong genetic differentiation between the two tortoise populations (Cerro Fatal and La Reserva) exhibiting domed shell morphology. Here we integrate nuclear microsatellite and mitochondrial data with statistical analyses of shell shape morphology to evaluate whether the genetic distinction and variability of the two domed tortoise populations is paralleled by differences in shell shape. Based on our results, morphometric analyses support the genetic distinction of the two populations and also reveal that the level of genetic variation is associated with morphological shell shape variation in both populations. The Cerro Fatal population possesses lower levels of morphological and genetic variation compared to the La Reserva population. Because the turtle shell is a complex heritable trait, our results suggest that, for the Cerro Fatal population, non-neutral loci have probably experienced a parallel decrease in variability as that observed for the genetic data. 相似文献
85.
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87.
Frias J; Bakhsh A; Jones D; Arthur A; Vidal-Valverde C; Rhodes M; Hedley C 《Journal of experimental botany》1999,50(333):469-476
Two lentil (Lens culinaris) cultivars, Syrian Local
Large (SLL) and PANT-L-406 (PL), have been used to study the genetics of
the raffinose family of oligosaccharides (RFO) and a related compound,
ciceritol, which is a galactosyl cyclitol. The RFO and ciceritol are the
major soluble -galactosides in lentil
seeds. Crosses were made between the two lentil lines and the patterns of
inheritance for the total -galactoside
content and for individual RFO compounds (raffinose, stachyose, verbascose)
and ciceritol were determined in the embryos and seed coats from single
seeds of the reciprocal F1s, the F2s and ten F3 families. The inheritance
patterns for each of the -galactosides were complex and much of
this complexity was attributed to an interaction between the embryo and its
surrounding testa. A clear-cut segregation pattern was observed for
verbascose. This was the result of PL embryos having very low, or no,
verbascose. The F2 embryos had a segregation ratio of 3 high to 1 low level
for this compound, suggesting that within this cross a low verbascose
content was determined by a single recessive gene. There was good evidence
from the F2 and F3 generations of a negative correlation between low levels
of verbascose and high levels of ciceritol, which suggests a metabolic link
between the RFO pathway and the pathway leading to ciceritol. The data are
discussed in terms of defining strategies for genetically manipulating
the-galactoside composition in lentil seeds, such that their
negative effects on nutrition may be overcome without reducing
significantly their positive role in abiotic stress
resistance. 相似文献
88.
Phospholipase D (PLD) is emerging as a major player in many novel signaling pathways. Based on recent studies correlating membrane composition with enzyme function, we speculated that feeding of dietary lipids to the newborns has a major impact on brain PLD activity. To test this hypothesis, the rat dams were fed fat-free powder containing either safflower oil or fish oil, and a control powdered chow. The pups were weaned onto the diet and sacrificed at 30 days of age. PLD activity was measured by transphosphatidylation assays using rat brain membranes. This study shows that microsome GTPS-dependent PLD activity in rats fed safflower oil or fish oil was significantly reduced by 38% and 30% respectively compared to controls. Oleate-dependent PLD activity in the safflower oil group, however, was significantly increased by 38%. In contrast, synaptosome membrane (P2) GTPS-dependent PLD activity in rats consuming safflower oil was significantly increased by 29%, but there was no difference in oleate-dependent PLD activity. Likewise, no difference was observed in microsome oleate-dependent PLD and P2 GTPS-dependent PLD activity between the fish oil and the control groups. These results indicate that dietary lipid intake appears to modulate phospholipid metabolism and differential expression of PLD isozymes in the brain. 相似文献
89.
Salt cress. A halophyte and cryophyte Arabidopsis relative model system and its applicability to molecular genetic analyses of growth and development of extremophiles 总被引:16,自引:0,他引:16 下载免费PDF全文
90.
A fundamental role for KChIPs in determining the molecular properties and trafficking of Kv4.2 potassium channels 总被引:23,自引:0,他引:23
Shibata R Misonou H Campomanes CR Anderson AE Schrader LA Doliveira LC Carroll KI Sweatt JD Rhodes KJ Trimmer JS 《The Journal of biological chemistry》2003,278(38):36445-36454
Kv4 potassium channels regulate action potentials in neurons and cardiac myocytes. Co-expression of EF hand-containing Ca2+-binding proteins termed KChIPs with pore-forming Kv4 alpha subunits causes changes in the gating and amplitude of Kv4 currents (An, W. F., Bowlby, M. R., Betty, M., Cao, J., Ling, H. P., Mendoza, G., Hinson, J. W., Mattsson, K. I., Strassle, B. W., Trimmer, J. S., and Rhodes, K. J. (2000) Nature 403, 553-556). Here we show that KChIPs profoundly affect the intracellular trafficking and molecular properties of Kv4.2 alpha subunits. Co-expression of KChIPs1-3 causes a dramatic redistribution of Kv4.2, releasing intrinsic endoplasmic reticulum retention and allowing for trafficking to the cell surface. KChIP co-expression also causes fundamental changes in Kv4.2 steady-state expression levels, phosphorylation, detergent solubility, and stability that reconstitute the molecular properties of Kv4.2 in native cells. Interestingly, the KChIP4a isoform, which exhibits unique effects on Kv4 channel gating, does not exert these effects on Kv4.2 and negatively influences the impact of other KChIPs. We provide evidence that these KChIP effects occur through the masking of an N-terminal Kv4.2 hydrophobic domain. These studies point to an essential role for KChIPs in determining both the biophysical and molecular characteristics of Kv4 channels and provide a molecular basis for the dramatic phenotype of KChIP knockout mice. 相似文献