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91.
Evidence for ACD5 ceramide kinase activity involvement in Arabidopsis response to cold stress 下载免费PDF全文
Christelle Dutilleul Heidy Chavarria Nathalie Rézé Bruno Sotta Emmanuel Baudouin Isabelle Guillas 《Plant, cell & environment》2015,38(12):2688-2697
Although sphingolipids emerged as important signals for plant response to low temperature, investigations have been limited so far to the function of long‐chain base intermediates. The formation and function of ceramide phosphates (Cer‐Ps) in chilled Arabidopsis were explored. Cer‐Ps were analysed by thin layer chromatography (TLC) following in vivo metabolic radiolabelling. Ceramide kinase activity, gene expression and growth phenotype were determined in unstressed and cold‐stressed wild type (WT) and Arabidopsis ceramide kinase mutant acd5. A rapid and transient formation of Cer‐P occurs in cold‐stressed WT Arabidopsis plantlets and cultured cells, which is strongly impaired in acd5 mutant. Although concomitant, Cer‐P formation is independent of long‐chain base phosphate (LCB‐P) formation. No variation of ceramide kinase activity was measured in vitro in WT plantlets upon cold stress but the activity in acd5 mutant was further reduced by cold stress. At the seedling stage, acd5 response to cold was similar to that of WT. Nevertheless, acd5 seed germination was hypersensitive to cold and abscisic acid (ABA), and ABA‐dependent gene expression was modified in acd5 seeds when germinated at low temperature. Our data involve for the first time Cer‐P and ACD5 in low temperature response and further underline the complexity of sphingolipid signalling operating during cold stress. 相似文献
92.
Christelle Borel Pedro?G. Ferreira Federico Santoni Olivier Delaneau Alexandre Fort Konstantin?Y. Popadin Marco Garieri Emilie Falconnet Pascale Ribaux Michel Guipponi Ismael Padioleau Piero Carninci Emmanouil?T. Dermitzakis Stylianos?E. Antonarakis 《American journal of human genetics》2015,96(1):70-80
93.
Mineem Saliba Nick Ramalanjaona Sandrine Gulberti Isabelle Bertin-Jung Aline Thomas Samir Dahbi Chrystel Lopin-Bon Jean-Claude Jacquinet Christelle Breton Mohamed Ouzzine Sylvie Fournel-Gigleux 《The Journal of biological chemistry》2015,290(12):7658-7670
Among glycosaminoglycan (GAG) biosynthetic enzymes, the human β1,4-galactosyltransferase 7 (hβ4GalT7) is characterized by its unique capacity to take over xyloside derivatives linked to a hydrophobic aglycone as substrates and/or inhibitors. This glycosyltransferase is thus a prime target for the development of regulators of GAG synthesis in therapeutics. Here, we report the structure-guided design of hβ4GalT7 inhibitors. By combining molecular modeling, in vitro mutagenesis, and kinetic measurements, and in cellulo analysis of GAG anabolism and decorin glycosylation, we mapped the organization of the acceptor binding pocket, in complex with 4-methylumbelliferone-xylopyranoside as prototype substrate. We show that its organization is governed, on one side, by three tyrosine residues, Tyr194, Tyr196, and Tyr199, which create a hydrophobic environment and provide stacking interactions with both xylopyranoside and aglycone rings. On the opposite side, a hydrogen-bond network is established between the charged amino acids Asp228, Asp229, and Arg226, and the hydroxyl groups of xylose. We identified two key structural features, i.e. the strategic position of Tyr194 forming stacking interactions with the aglycone, and the hydrogen bond between the His195 nitrogen backbone and the carbonyl group of the coumarinyl molecule to develop a tight binder of hβ4GalT7. This led to the synthesis of 4-deoxy-4-fluoroxylose linked to 4-methylumbelliferone that inhibited hβ4GalT7 activity in vitro with a Ki 10 times lower than the Km value and efficiently impaired GAG synthesis in a cell assay. This study provides a valuable probe for the investigation of GAG biology and opens avenues toward the development of bioactive compounds to correct GAG synthesis disorders implicated in different types of malignancies. 相似文献
94.
Johanna Ceschin Hans Caspar Hürlimann Christelle Saint-Marc Delphine Albrecht Typhaine Violo Michel Moenner Bertrand Daignan-Fornier Beno?t Pinson 《The Journal of biological chemistry》2015,290(39):23947-23959
5-Aminoimidazole-4-carboxamide-1-β-d-ribofuranoside monophosphate (AICAR) is a natural metabolite with potent anti-proliferative and low energy mimetic properties. At high concentration, AICAR is toxic for yeast and mammalian cells, but the molecular basis of this toxicity is poorly understood. Here, we report the identification of yeast purine salvage pathway mutants that are synthetically lethal with AICAR accumulation. Genetic suppression revealed that this synthetic lethality is in part due to low expression of adenine phosphoribosyl transferase under high AICAR conditions. In addition, metabolite profiling points to the AICAR/NTP balance as crucial for optimal utilization of glucose as a carbon source. Indeed, we found that AICAR toxicity in yeast and human cells is alleviated when glucose is replaced by an alternative carbon source. Together, our metabolic analyses unveil the AICAR/NTP balance as a major factor of AICAR antiproliferative effects. 相似文献
95.
Quentin Bruggeman Florence Prunier Christelle Mazubert Linda de Bont Marie Garmier Rapha?l Lugan Moussa Benhamed Catherine Bergounioux Cécile Raynaud Marianne Delarue 《The Plant cell》2015,27(6):1801-1814
Programmed cell death (PCD) is essential for several aspects of plant life, including development and stress responses. We recently identified the mips1 mutant of Arabidopsis thaliana, which is deficient for the enzyme catalyzing the limiting step of myo-inositol (MI) synthesis. One of the most striking features of mips1 is the light-dependent formation of lesions on leaves due to salicylic acid (SA)-dependent PCD. Here, we identified a suppressor of PCD by screening for mutations that abolish the mips1 cell death phenotype. Our screen identified the hxk1 mutant, mutated in the gene encoding the hexokinase1 (HXK1) enzyme that catalyzes sugar phosphorylation and acts as a genuine glucose sensor. We show that HXK1 is required for lesion formation in mips1 due to alterations in MI content, via SA-dependant signaling. Using two catalytically inactive HXK1 mutants, we also show that hexokinase catalytic activity is necessary for the establishment of lesions in mips1. Gas chromatography-mass spectrometry analyses revealed a restoration of the MI content in mips1 hxk1 that it is due to the activity of the MIPS2 isoform, while MIPS3 is not involved. Our work defines a pathway of HXK1-mediated cell death in plants and demonstrates that two MIPS enzymes act cooperatively under a particular metabolic status, highlighting a novel checkpoint of MI homeostasis in plants. 相似文献
96.
Christelle Péré Robert Bell Ted C. J. Turlings Marc Kenis 《Biodiversity and Conservation》2011,20(13):3003-3016
Apparent competition, through the action of shared natural enemies, is frequently suggested as a possible mechanism underlying
the impact of invasive alien species on native species, but examples are rare, particularly in insects. A previous study showed
that the beech leaf mining weevil, Orchestes fagi, was significantly less abundant close to horse-chestnut trees infested by the invasive horse-chestnut leaf mining moth,
Cameraria ohridella, compared to control sites. Apparent competition through the sharing of natural enemies was proposed as a potential mechanism
underlying this effect. To test the occurrence of apparent competition between the two leaf miner species, three observational
studies and one experimental manipulation were carried out in Switzerland during 3 years. The total mortality, parasitism,
predation and parasitoid diversity of larvae and pupae of O. fagi were compared between sites with and without horse-chestnut trees severely attacked by C. ohridella. Total mortality and predation rates of O. fagi were not significantly different between sites with and sites without C. ohridella. Despite a large overlap between the parasitoid complexes of the two leaf miners, parasitism of O. fagi was found to be positively influenced by the presence of horse-chestnuts infested by C. ohridella in only one of the four studies and only for 1 year. Similarly, parasitoid diversity was not higher near infested horse-chestnut
trees compared to control sites. Thus, little evidence for apparent competition was found. Possible reasons, including possible
insufficiencies in the experimental circumstances and design, are discussed. 相似文献
97.
98.
99.
Sainlos M Tigaret C Poujol C Olivier NB Bard L Breillat C Thiolon K Choquet D Imperiali B 《Nature chemical biology》2011,7(2):81-91
The interactions of the AMPA receptor (AMPAR) auxiliary subunit Stargazin with PDZ domain-containing scaffold proteins such as PSD-95 are critical for the synaptic stabilization of AMPARs. To investigate these interactions, we have developed biomimetic competing ligands that are assembled from two Stargazin-derived PSD-95/DLG/ZO-1 (PDZ) domain-binding motifs using 'click' chemistry. Characterization of the ligands in vitro and in a cellular FRET-based model revealed an enhanced affinity for the multiple PDZ domains of PSD-95 compared to monovalent peptides. In cultured neurons, the divalent ligands competed with transmembrane AMPAR regulatory protein (TARP) for the intracellular membrane-associated guanylate kinase resulting in increased lateral diffusion and endocytosis of surface AMPARs, while showing strong inhibition of synaptic AMPAR currents. This provides evidence for a model in which the TARP-containing AMPARs are stabilized at the synapse by engaging in multivalent interactions. In light of the prevalence of PDZ domain clusters, these new biomimetic chemical tools could find broad application for acutely perturbing multivalent complexes. 相似文献
100.
Waligora-Dupriet AJ Campeotto F Romero K Mangin I Rouzaud G Ménard O Suau A Soulaines P Nicolis I Kapel N Dupont C Butel MJ 《Anaerobe》2011,17(3):91-96
Some clinical studies have suggested a relationship between allergic diseases and gut microbiota. We aimed to study bifidobacterial colonization at species and strain levels in ten allergic French infants included at their first clinical consultation and 20 controls matching for age at sampling, mode of delivery, per partum antibiotics, type of feeding and antibiotics in the first weeks of life. The faecal microbiota was analyzed by culture methods and TTGE. Bifidobacterial species and strains were identified using multiplex PCR and Box-PCR fingerprinting. No differences were observed between groups in the number of colonized infants or in the levels of colonization by the main aerobic and anaerobic genera. All infants were colonized with high levels of Bifidobacterium except for one in each group. One to 5 Bifidobacterium species and 1 to 7 strains were observed per subject independently of allergic status and age at sampling. Our study showed the infants to be colonized by several species and strains, including several strains from the same species. This diversity in Bifidobacterium colonization was not related with the allergic status and showed that the link between Bifidobacterium colonization and allergic diseases is complex and cannot be restricted to the role attributed to Bifidobacterium species. 相似文献