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21.
Moreau D Burstin J Aubert G Huguet T Ben C Prosperi JM Salon C Munier-Jolain N 《TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik》2012,124(4):755-768
Medicago truncatula is used as a model plant for exploring the genetic and molecular determinants of nitrogen (N) nutrition in legumes. In this
study, our aim was to detect quantitative trait loci (QTL) controlling plant N nutrition using a simple framework of carbon/N
plant functioning stemming from crop physiology. This framework was based on efficiency variables which delineated the plant’s
efficiency to take up and process carbon and N resources. A recombinant inbred line population (LR4) was grown in a glasshouse
experiment under two contrasting nitrate concentrations. At low nitrate, symbiotic N2 fixation was the main N source for plant growth and a QTL with a large effect located on linkage group (LG) 8 affected all
the traits. Significantly, efficiency variables were necessary both to precisely localize a second QTL on LG5 and to detect
a third QTL involved in epistatic interactions on LG2. At high nitrate, nitrate assimilation was the main N source and a larger
number of QTL with weaker effects were identified compared to low nitrate. Only two QTL were common to both nitrate treatments:
a QTL of belowground biomass located at the bottom of LG3 and another one on LG6 related to three different variables (leaf
area, specific N uptake and aboveground:belowground biomass ratio). Possible functions of several candidate genes underlying
QTL of efficiency variables could be proposed. Altogether, our results provided new insights into the genetic control of N
nutrition in M. truncatula. For instance, a novel result for M. truncatula was identification of two epistatic interactions in controlling plant N2 fixation. As such this study showed the value of a simple conceptual framework based on efficiency variables for studying
genetic determinants of complex traits and particularly epistatic interactions. 相似文献
22.
Mohamed Alburaki Sébastien Boutin Pierre-Luc Mercier Yves Loublier Madeleine Chagnon Nicolas Derome 《PloS one》2015,10(5)
Thirty-two honeybee (Apis mellifera) colonies were studied in order to detect and measure potential in vivo effects of neonicotinoid pesticides used in cornfields (Zea mays spp) on honeybee health. Honeybee colonies were randomly split on four different agricultural cornfield areas located near Quebec City, Canada. Two locations contained cornfields treated with a seed-coated systemic neonicotinoid insecticide while the two others were organic cornfields used as control treatments. Hives were extensively monitored for their performance and health traits over a period of two years. Honeybee viruses (brood queen cell virus BQCV, deformed wing virus DWV, and Israeli acute paralysis virus IAPV) and the brain specific expression of a biomarker of host physiological stress, the Acetylcholinesterase gene AChE, were investigated using RT-qPCR. Liquid chromatography-mass spectrometry (LC-MS) was performed to detect pesticide residues in adult bees, honey, pollen, and corn flowers collected from the studied hives in each location. In addition, general hive conditions were assessed by monitoring colony weight and brood development. Neonicotinoids were only identified in corn flowers at low concentrations. However, honeybee colonies located in neonicotinoid treated cornfields expressed significantly higher pathogen infection than those located in untreated cornfields. AChE levels showed elevated levels among honeybees that collected corn pollen from treated fields. Positive correlations were recorded between pathogens and the treated locations. Our data suggests that neonicotinoids indirectly weaken honeybee health by inducing physiological stress and increasing pathogen loads. 相似文献
23.
Genetic and plastic responses of a northern mammal to climate change 总被引:11,自引:0,他引:11
Réale D McAdam AG Boutin S Berteaux D 《Proceedings. Biological sciences / The Royal Society》2003,270(1515):591-596
Climate change is predicted to be most severe in northern regions and there has been much interest in to what extent organisms can cope with these changes through phenotypic plasticity or microevolutionary processes. A red squirrel population in the southwest Yukon, Canada, faced with increasing spring temperatures and food supply has advanced the timing of breeding by 18 days over the last 10 years (6 days per generation). Longitudinal analysis of females breeding in multiple years suggests that much of this change in parturition date can be explained by a plastic response to increased food abundance (3.7 days per generation). Significant changes in breeding values (0.8 days per generation), were in concordance with predictions from the breeder's equation (0.6 days per generation), and indicated that an evolutionary response to strong selection favouring earlier breeders also contributed to the observed advancement of this heritable trait. The timing of breeding in this population of squirrels, therefore, has advanced as a result of both phenotypic changes within generations, and genetic changes among generations in response to a rapidly changing environment. 相似文献
24.
Isabelle Cloëz Ivan Tayarani Frédérique Morel Jean-Marie Bourre 《Journal of neurochemistry》1989,52(5):1353-1358
The activities of peroxide-detoxifying enzymes such as superoxide dismutase (SOD), glutathione peroxidase, glutathione reductase, and catalase were measured in the nervous system of neurological dysmyelinating mutants: quaking (Qk), shiverer (Shi), and trembler (Tr) mice. Cu/Zn-SOD activity was higher in the cerebellum of Qk and Shi mice (by 53% and 106%, respectively) in comparison with controls, but it was the same in the cerebellum of Tr mice and their corresponding controls. In contrast, there was no difference in the level of Cu/Zn-SOD activity in the cerebrum of Qk, Shi, and Tr mice and their respective controls. Mn-SOD activity was the same among all the mutants compared to control animals in both cerebrum and cerebellum. In Shi cerebellum, glutathione peroxidase and glutathione reductase activities were slightly decreased (a 21.6% and a 13.2% diminution, respectively), whereas catalase activity in cerebrum and cerebellum was the same among mutants and control mice. In the sciatic nerve from Tr mice, all the enzymatic activities were enhanced: sixfold increase for total SOD, and 2.4-fold, 3.5-fold, and 1.8-fold increase for glutathione peroxidase, glutathione reductase, and catalase, respectively. 相似文献
25.
Lucie Khemtémourian Sébastien Lavielle Katell Bathany Jean-Marie Schmitter Erick J Dufourc 《Journal of peptide science》2006,12(5):361-368
Solid-phase syntheses of the hydrophobic peptides Neu(TM35) ((1)EQRASPVTFIIATVVGVLLFLILVVVVGILIKRRR(35)) and Neu*(TM35) ((1)EQRASPVTFIIATVEGVLLFLILVVVVGILIKRRR(35)), corresponding to the native and mutated (V15E) transmembrane domain of the neu/erbB-2 tyrosine kinase receptor, respectively, were accomplished using Fmoc chemistry. The use of a new resin and cleavage and purification conditions led to large increases in yields and peptide purity. Two (15)N-labelled versions of both wild type and mutated peptides were also synthesized. Approximately 20-40 mg of peptide was obtained using a small-scale synthesis, whereas ca 100 mg of pure peptide was collected on a medium scale. Peptide purity, as monitored by HPLC and mass spectrometry, ranged from 95 to 98% for the six peptides synthesized. Secondary structure as determined by UV circular dichroism (CD) in trifluoroethanol (TFE) showed ca 74% alpha-helical content for the native peptide and ca 63% for that bearing the mutation. Secondary structure of Neu(TM35) was retained in DMPC (dimyristoylphosphatidylcholine)/DCPC (dicaproylphosphatidylcholine) membrane bicelles, and evidences for dimers/oligomers in the lipid bilayer were found. 相似文献
26.
Abid G Muhovski Y Jacquemin JM Mingeot D Sassi K Toussaint A Baudoin JP 《Molecular biology reports》2012,39(2):1133-1143
A full-length cDNA encoding common bean (Phaseolus vulgaris L.) sucrose synthase (designated as Pv_BAT93 Sus), which catalyses the synthesis and cleavage of sucrose, was isolated from
seeds at 15 days after pollination (DAP) by rapid amplification of cDNA ends (RACE). The full-length cDNA of Pv_BAT93 Sus
had a 2,418 bp open reading frame (ORF) encoding a protein of 806 amino acid residues. Sequence comparison analysis showed
that Pv_BAT93 Sus was very similar to several members of the sucrose synthase family of other plant species. Tissue expression
pattern analysis showed that Pv_BAT93 Sus was expressed in leaves, flowers, stems, roots, cotyledons, and particularly during
seed development. Expression studies using in situ hybridization revealed altered spatial and temporal patterns of Sus expression
in the EMS mutant relative to wild-type and confirmed Sus expression in common bean developing seeds. The expression and accumulation
of Sus mRNA was clearly shown in several tissues, such as the suspensor and embryo, but also in the transfer cells and endothelium.
The results highlight the diverse roles that Sus might play during seed development in common bean. 相似文献
27.
Marwen Moussa Vincent Espinasse Jean-Marie Perrier-Cornet Patrick Gervais 《Applied microbiology and biotechnology》2009,85(1):165-174
We investigated the influence of cell hydration on the ability of Saccharomyces cerevisiae CBS 1171 to withstand extreme hydrostatic pressure in order to determine the mechanisms involved in cell resistance. Hydration
conditions were modified in two different ways. We first modulated the chemical potential of water by adding glycerol in cell
suspensions. Another procedure consisted in dehydrating cells aerobically and immersing them in perfluorooctane, an innocuous
hydrophobic liquid used as a pressure-transmitting medium, prior to pressure treatments. This original method made it possible
to transmit isostatic pressure to yeast powders without changing the initial water activity (a
w) level at which cells had been equilibrated. The a
w ranged between 0.11 and 0.99. Pressure treatments were applied at levels of up to 600 MPa for 10 min, 24 h, and 6 days. The
dehydration of cells was found to strongly limit, or even prevent, cell inactivation under pressure. Notably, cells suspended
in a water–glycerol mixture with a
w levels of 0.71 or below were completely protected against all pressure treatments. Moreover, cells dehydrated aerobically
survived for 6 days at 600 MPa even when a
w levels were relatively high (up to 0.94). We highlighted the crucial role of water content in determining cellular damage
under pressure. When water is available in a sufficient amount, high pressure induces membrane permeabilization, causing uncontrolled
mass transfers that could lead to death during a prolonged holding under pressure. Possible mechanisms of membrane permeabilization
are discussed. 相似文献
28.
Dominique Toussaint-Demylle Jean-Marie Scheiff Stanislas Haumont 《Cell and tissue research》1990,262(1):115-123
Summary Thymic nurse cells (TNC), which are multicellular complexes composed of epithelial cells and thymocytes, were obtained from C3H-mice thymuses. They were described by means of light and electron microscopy. The morphology of epithelial cells forming isolated TNC compared to that of small tissue fragments obtained by enzymatic digestion revealed that TNC could be derived from all parts of the thymus: cortex, corticomedullary junction and medulla, the cortex being their principal source. This variety of origin, the presence of several epithelial cells inside a single TNC, the presence of non-lymphoid cells, and the various locations of eleaved desmosomes confirmed that their aspect in vitro as round and sealed structures can be considered to be an artifact due to the isolation technique used. Indeed, during this procedure, they are formed by a process of wrapping of the epithelial cytoplasm around the tightly associated thymocytes. All three epithelial cell types: cortical reticular cells, medullary reticular cells, and medullary globular cells can form TNC.A portion of this work was presented at the first Thymus Workshop. Rolduc, Netherlands, April, 1988 相似文献
29.
Analysis of lambda receptor and beta-lactamase synthesis and export using cloned genes in a minicell system 总被引:8,自引:0,他引:8
Jean-Marie Clement David Perrin Joe Hedgpeth 《Molecular & general genetics : MGG》1982,185(2):302-310
Summary We have cloned lamB, the gene for receptor (an outer membrane protein), on a small plasmid which also carries the gene for -lactamase (a periplasmic protein). We have identified a promoter in the region of malK, the gene immediately preceding lamB, which is active in minicells but relatively inactive in vitro. Using a minicell system, we have found that both receptor and -lactamase are made as full length precursors which are subsequently processed. We also show that the receptor precursor can be exported to the outer membrane before it is processed. Mature -lactamase is found only in the periplasm, suggesting that processing may be a requirement for export to the periplasm. 相似文献
30.
Séron K Corset L Vasseur F Boutin P Gómez-Ambrosi J Salvador J Frühbeck G Froguel P 《Biochemical and biophysical research communications》2006,348(4):1232-1238
Animal studies have illustrated the importance of the expression in adipose tissue of the leptin receptor (OB-R), and of SOCS3 an inhibitor of the leptin signaling pathway, in body weight regulation. The aim of the present study was to investigate in human adipose tissues of the same patients the OB-R isoforms and SOCS3 expression. Subcutaneous and omental adipose tissues were obtained from 6 lean and 18 morbidly obese women. The long isoform OB-Rb mRNA mediating leptin signaling, and SOCS3 mRNA are abundantly present in the subcutaneous fat of lean women, but are 90% and 70% decreased (P<0.0001) in obese women. In visceral fat from lean and obese women, both OB-Rb and SOCS3 mRNA are detected at very low levels. Subcutaneous/visceral ratios for OB-Ra the short OB-R isoform, OB-Rb, and SOCS3 mRNA abundance strongly correlate with the insulin sensitivity index, HOMA-% S, (r=0.49, P<0.0001, r=0.42, P=0.0002 and r=0.38, P=0.0002, respectively) in both lean and obese patients without type 2 diabetes. The near absence of OB-Rb mRNA and the similarly decreased SOCS3 expression in obese adipose tissue may reflect a defective leptin signaling pathway that could play a role in the impairment of insulin sensitivity associated with excess adiposity. 相似文献