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101.
Pennarun G Granotier C Hoffschir F Mandine E Biard D Gauthier LR Boussin FD 《Nucleic acids research》2008,36(5):1741-1754
Telomeres are known to prevent chromosome ends from being recognized as DNA double-strand breaks. Conversely, many DNA damage response proteins, including ATM, are thought to participate to telomere maintenance. However, the precise roles of ATM at telomeres remain unclear due to its multiple functions in cell checkpoints and apoptosis. To gain more insights into the role of ATM in telomere maintenance, we determined the effects of the G-quadruplex ligand 360A in various cell lines lacking functional ATM. We showed, by using Fluorescence in situ hybridization (FISH) and Chromosome Orientation-FISH using telomere PNA probes, that 360A induced specific telomere aberrations occurring during or after replication, mainly consisting in sister telomere fusions and also recombinations that involved preferentially the lagging strand telomeres. We demonstrate that ATM reduced telomere instability independently of apoptosis induction. Our results suggest thus that ATM has a direct role in preventing inappropriate DNA repair at telomeres, which could be related to its possible participation to the formation of protected structures at telomeres. 相似文献
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103.
Lionel Guittat Patrizia Alberti Dennis Gomez Anne De Cian Gaëlle Pennarun Thibault Lemarteleur Chafke Belmokhtar Rajaa Paterski Hamid Morjani Chantal Trentesaux Eliane Mandine François Boussin Patrick Mailliet Laurent Lacroix Jean-François Riou Jean-Louis Mergny 《Cytotechnology》2004,45(1-2):75-90
The enzyme telomerase is involved in the replication of telomeres, specialized structures that cap and protect the ends of chromosomes. Its activity is required for maintenance of telomeres and for unlimited lifespan, a hallmark of cancer cells. Telomerase is overexpressed in the vast majority of human cancer cells and therefore represents an attractive target for therapy. Several approaches have been developed to inhibit this enzyme through the targeting of its RNA or catalytic components as well as its DNA substrate, the single-stranded 3′-telomeric overhang. Telomerase inhibitors are chemically diverse and include modified oligonucleotides as well as small diffusable molecules, both natural and synthetic. This review presents an update of recent investigations pertaining to these agents and discusses their biological properties in the context of the initial paradigm that the exposure of cancer cells to these agents should lead to progressive telomere shortening followed by a delayed growth arrest response. 相似文献
104.
Sophie Slezack Jonathan Negrel Gwénaëlle Bestel-Corre Eliane Dumas-Gaudot Silvio Gianinazzi 《Planta》2001,213(5):781-787
Colonization of Pisum sativum L. cv. Frisson roots with the arbuscular mycorrhizal fungus Glomus mosseae leads to the induction of four acidic symbiosis-related chitinase (SR-chi) isoforms (EC 3.2.1.14). These isoforms were characterized as 30-kDa proteins with isoelectric points ranging between 5.2 and 5.85. One of these SR-chis was purified by affinity and anion-exchange chromatographies, and isoelectric focusing electrophoresis. The sequences of four internal peptides were obtained. They showed high homology to a class-I chitinase isoform from pea shoots. Parts of the conserved regions of class-I chitinases were found in this SR-chi. This result strongly supports the argument that this SR-chi isoform is of plant origin. The functional role of the SR-chis in arbuscular mycorrhizal symbiosis is discussed. 相似文献
105.
We describe here a novel methodology for rapid diagnosis of metabolic changes, which is based on probabilistic equations that relate GC-MS-derived mass distributions in proteinogenic amino acids to in vivo enzyme activities. This metabolic flux ratio analysis by GC-MS provides a comprehensive perspective on central metabolism by quantifying 14 ratios of fluxes through converging pathways and reactions from [1-13C] and [U-13C]glucose experiments. Reliability and accuracy of this method were experimentally verified by successfully capturing expected flux responses of Escherichia coli to environmental modifications and seven knockout mutations in all major pathways of central metabolism. Furthermore, several mutants exhibited additional, unexpected flux responses that provide new insights into the behavior of the metabolic network in its entirety. Most prominently, the low in vivo activity of the Entner-Doudoroff pathway in wild-type E. coli increased up to a contribution of 30% to glucose catabolism in mutants of glycolysis and TCA cycle. Moreover, glucose 6-phosphate dehydrogenase mutants catabolized glucose not exclusively via glycolysis, suggesting a yet unidentified bypass of this reaction. Although strongly affected by environmental conditions, a stable balance between anaplerotic and TCA cycle flux was maintained by all mutants in the upper part of metabolism. Overall, our results provide quantitative insight into flux changes that bring about the resilience of metabolic networks to disruption. 相似文献
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107.
Johara Boldrini-França Renata Santos Rodrigues Ludier Kesser Santos-Silva Dayane Lorena Naves de Souza Mário Sérgio Rocha Gomes Camila Takeno Cologna Edwin de Pauw Loïc Quinton Flávio Henrique-Silva Veridiana de Melo Rodrigues Eliane Candiani Arantes 《Applied microbiology and biotechnology》2015,99(23):9971-9986
108.
Roberta Bianchi Eliane Fischer Don Yuen Ellen Ernst Alexandra M. Ochsenbein Lu Chen Vivianne I. Otto Michael Detmar 《The Journal of biological chemistry》2014,289(30):21016-21027
The lymphatic system plays an important role in cancer metastasis and inhibition of lymphangiogenesis could be valuable in fighting cancer dissemination. Podoplanin (Pdpn) is a small, transmembrane glycoprotein expressed on the surface of lymphatic endothelial cells (LEC). During mouse development, binding of Pdpn to the C-type lectin-like receptor 2 (CLEC-2) on platelets is critical for the separation of the lymphatic and blood vascular systems. Competitive inhibition of Pdpn functions with a soluble form of the protein, Pdpn-Fc, leads to reduced lymphangiogenesis in vitro and in vivo. However, the transgenic overexpression of human Pdpn-Fc in mouse skin causes disseminated intravascular coagulation due to platelet activation via CLEC-2. In the present study, we produced and characterized a mutant form of mouse Pdpn-Fc, in which threonine 34, which is considered essential for CLEC-2 binding, was mutated to alanine (PdpnT34A-Fc). Indeed, PdpnT34A-Fc displayed a 30-fold reduced binding affinity for CLEC-2 compared with Pdpn-Fc. This also translated into fewer side effects due to platelet activation in vivo. Mice showed less prolonged bleeding time and fewer embolized vessels in the liver, when PdpnT34A-Fc was injected intravenously. However, PdpnT34A-Fc was still as active as wild-type Pdpn-Fc in inhibiting lymphangiogenesis in vitro and also inhibited lymphangiogenesis in vivo. These data suggest that the function of Pdpn in lymphangiogenesis does not depend on threonine 34 in the CLEC-2 binding domain and that PdpnT34A-Fc might be an improved inhibitor of lymphangiogenesis with fewer toxic side effects. 相似文献
109.
Pachycondyla marginata (P.m.), a migratory and termitophageous ant, hunting only the termite species Neocapritermes opacus, migrates significantly oriented 13 degrees with respect to the magnetic North-South axis. Results of hysteresis curves at room temperature of four Pachycondyla marginata heads, thorax, pairs of antennae and abdomens, oriented parallel to the magnetic field, indicate that the antennae give the strongest saturation magnetization, suggesting this sensory organ as being also a magnetic sensory organ. The total saturation magnetization in a whole P.m. is composed by 42 +/- 3%, 24 +/- 3%, 19 +/- 3% and 15 +/- 3% of antennae, head, thorax and abdomen contributions, respectively. The abdomen hysteresis curve presents a wasp-waisted loop with Hcr/Hc of 4.75, characteristic of mixed magnetic systems. 相似文献
110.