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31.
Lionel Dégremont Jean-Baptiste Lamy Jean-Fran?ois Pépin Marie-Agnès Travers Tristan Renault 《PloS one》2015,10(6)
The Pacific oyster, Crassostrea gigas, is the most important commercial oyster species cultivated in the world. Meanwhile, the ostreid herpesvirus 1 (OsHV-1) is one of the major pathogens affecting the Pacific oyster, and numerous mortality outbreaks related to this pathogen are now reported worldwide. To assess the genetic basis of resistance to OsHV-1 infection in spat C. gigas and to facilitate breeding programs for such a trait, if any exist, we compared the mortality of half- and full-sib families using three field methods and a controlled challenge by OsHV-1 in the laboratory. In the field, three methods were tested: (A) one family per bag; (B) one family per small soft mesh bag and all families inside one bag; (C) same as the previous methods but the oysters were individually labelled and then mixed. The mean mortality ranged from 80 to 82% and was related to OsHV-1 based on viral DNA detection. The narrow-sense heritability for mortality, and thus OsHV-1 resistance, ranged from 0.49 to 0.60. The high positive genetic correlations across the field methods suggested no genotype by environment interaction. Ideally, selective breeding could use method B, which is less time- and space-consuming. The narrow sense heritability for mortality under OsHV-1 challenge was 0.61, and genetic correlation between the field and the laboratory was ranged from 0.68 to 0.75, suggesting a weak genotype by environment interaction. Thus, most of families showing the highest survival performed well in field and laboratory conditions, and a similar trend was also observed for families with the lowest survival. In conclusion, this is the first study demonstrating a large additive genetic variation for resistance to OsHV-1 infection in C. gigas, regardless of the methods used, which should help in selective breeding to improve resistance to viral infection in C. gigas. 相似文献
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35.
Vassili Valayannopoulos Coralie Haudry Valérie Serre Magalie Barth Nathalie Boddaert Jean-Baptiste Arnoux Valérie Cormier-Daire Marlène Rio Daniel Rabier Anne Vassault Arnold Munnich Jean-Paul Bonnefont Pascale de Lonlay Agnès Rötig Anne-Sophie Lebre 《Mitochondrion》2010,10(4):335-341
Deficiencies in two subunits of the succinyl-coenzyme A synthetase (SCS) have been involved in patients with encephalomyopathy and mild methylmalonic aciduria (MMA). In this study, we described three new SUCLG1 patients and performed a meta-analysis of the literature. Our report enlarges the phenotypic spectrum of SUCLG1 mutations and confirms that a characteristic metabolic profile (presence of MMA and C4-DC carnitine in urines) and basal ganglia MRI lesions are the hallmarks of SCS defects. As mitochondrial DNA depletion in muscle is not a constant finding in SUCLG1 patients, this may suggest that diagnosis should not be based on it, but also that alternative physiopathological mechanisms may be considered to explain the combined respiratory chain deficiency observed in SCS patients. 相似文献
36.
The preferential use of one hand over the other is considered the primary behavioral expression of structural and functional asymmetry in cerebral structures, which is a decisive factor in human evolution. We present the first analysis of manual laterality in a form of object play—stone handling (SH) behavior—in a free-ranging group of Japanese macaques. Defined as a stone-directed manipulative activity, and comprised of multiple one-handed SH patterns (e.g., grabbing a stone in one hand and cradling it against its chest), as well as coordinated two-handed SH patterns with manual role differentiation (e.g., holding a stone with one hand and rubbing it with the other), SH behavior is a good candidate for the study of hand lateralization. We systematically followed the methodological framework developed by McGrew and Marchant (1997) to measure and analyze the presence, strength, and direction of manual preference in the performance of SH behavior and in various SH patterns, both at the individual and group level. Some individuals showed a significant manual lateral bias on a single SH pattern (hand preference), whereas others showed consistency in laterality across all or most of the SH patterns they performed (hand specialization). At the group level, we found that, although their collective distribution of left versus right remained random, most subjects were either significantly but incompletely lateralized, or completely lateralized within particular SH patterns (pattern specialization), but not across all SH patterns (no handedness for SH behavior as a whole). As predicted by the task-complexity model, hand specialization and handedness were stronger in the coordinated bimanual SH patterns than in the unimanual patterns. We discuss the implications of our findings for the evolution of manual preferences in noninstrumental object manipulation versus stone tool use in nonhuman primates and hominins. 相似文献
37.
Peter J. Fashing Felix Mulindahabi Jean-Baptiste Gakima Michel Masozera Ian Mununura Andrew J. Plumptre Nga Nguyen 《International journal of primatology》2007,28(3):529-550
With group sizes sometimes >300 individuals, the Angolan black-and-white colobus (Colobus angolensis ruwenzorii) population
in Nyungwe Forest, Rwanda is an intriguing exception to the tendency for folivores to live in smaller groups than expected
relative to body size. Researchers have hypothesized that the unusually high quality of foliage at Nyungwe allows colobus
there to avoid intragroup feeding competition, releasing constraints on the formation of large groups (Fimbel et al., 2001). We collected data on the activity and ranging patterns of a >300-member Nyungwe colobus group and compared our results
to those from smaller groups in other black-and-white colobus (Colobus spp.) populations. Colobus at Nyungwe spent far more
time feeding and moving (62%) and far less time resting (32%) than black-and-white colobus at any other site. The annual home
range of the Nyungwe colobus was also many times larger (95% minimum convex polygon: 20.7 km
2
; 95% fixed kernel: 24.4 km
2
) than those for other populations. We terminated our research after the group engaged in an unprecedented migration among
black-and-white colobus by moving 13 km south of their former range. Our results suggest that intragroup scramble competition
may be more intense than originally believed within the large colobus groups at Nyungwe and that long periods of resource
renewal may be necessary after a large colobus group passes through an area, thereby potentially helping to explain their
wide ranging patterns. We discuss the socioecological convergence between the Nyungwe colobus and Chinese snub-nosed monkeys
(Rhinopithecus spp.) and suggest directions for future research on the unique black-and-white colobus population at Nyungwe.
相似文献
Peter J. FashingEmail: |
38.
Julier B Huguet T Chardon F Ayadi R Pierre JB Prosperi JM Barre P Huyghe C 《TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik》2007,114(8):1391-1406
In many legume crops, especially in forage legumes, aerial morphogenesis defined as growth and development of plant organs,
is an essential trait as it determines plant and seed biomass as well as forage quality (protein concentration, dry matter
digestibility). Medicago truncatula is a model species for legume crops. A set of 29 accessions of M. truncatula was evaluated for aerial morphogenetic traits. A recombinant inbred lines (RILs) mapping population was used for analysing
quantitative variation in aerial morphogenetic traits and QTL detection. Genes described to be involved in aerial morphogenetic
traits in other species were mapped to analyse co-location between QTLs and genes. A large variation was found for flowering
date, morphology and dynamics of branch elongation among the 29 accessions and within the RILs population. Flowering date
was negatively correlated to main stem and branch length. QTLs were detected for all traits, and each QTL explained from 5.2
to 59.2% of the phenotypic variation. A QTL explaining a large part of genetic variation for flowering date and branch growth
was found on chromosome 7. The other chromosomes were also involved in the variation detected in several traits. Mapping of
candidate genes indicates a co-location between a homologue of Constans gene or a flowering locus T (FT) gene and the QTL
of flowering date on chromosome 7. Other candidate genes for several QTLs are described.
Electronic supplementary material The online version of this article (doi:) contains supplementary material, which is available to authorized users. 相似文献
39.
Garlatti V Martin L Gout E Reiser JB Fujita T Arlaud GJ Thielens NM Gaboriaud C 《The Journal of biological chemistry》2007,282(49):35814-35820
Ficolins are soluble oligomeric proteins with lectin-like activity, assembled from collagen fibers prolonged by fibrinogen-like recognition domains. They act as innate immune sensors by recognizing conserved molecular markers exposed on microbial surfaces and thereby triggering effector mechanisms such as enhanced phagocytosis and inflammation. In humans, L- and H-ficolins have been characterized in plasma, whereas a third species, M-ficolin, is secreted by monocytes and macrophages. To decipher the molecular mechanisms underlying their recognition properties, we previously solved the structures of the recognition domains of L- and H-ficolins, in complex with various model ligands (Garlatti, V., Belloy, N., Martin, L., Lacroix, M., Matsushita, M., Endo, Y., Fujita, T., Fontecilla-Camps, J. C., Arlaud, G. J., Thielens, N. M., and Gaboriaud, C. (2007) EMBO J. 24, 623-633). We now report the ligand-bound crystal structures of the recognition domain of M-ficolin, determined at high resolution (1.75-1.8 A), which provides the first structural insights into its binding properties. Interaction with acetylated carbohydrates differs from the one previously described for L-ficolin. This study also reveals the structural determinants for binding to sialylated compounds, a property restricted to human M-ficolin and its mouse counterpart, ficolin B. Finally, comparison between the ligand-bound structures obtained at neutral pH and nonbinding conformations observed at pH 5.6 reveals how the ligand binding site is dislocated at acidic pH. This means that the binding function of M-ficolin is subject to a pH-sensitive conformational switch. Considering that the homologous ficolin B is found in the lysosomes of activated macrophages (Runza, V. L., Hehlgans, T., Echtenacher, B., Zahringer, U., Schwaeble, W. J., and Mannel, D. N. (2006) J. Endotoxin Res. 12, 120-126), we propose that this switch could play a physiological role in such acidic compartments. 相似文献
40.
Structural and thermodynamic bases for the design of pure prolactin receptor antagonists: X-ray structure of Del1-9-G129R-hPRL 总被引:2,自引:0,他引:2
Jomain JB Tallet E Broutin I Hoos S van Agthoven J Ducruix A Kelly PA Kragelund BB England P Goffin V 《The Journal of biological chemistry》2007,282(45):33118-33131
Competitive antagonists of the human prolactin (hPRL) receptor are a novel class of molecules of potential therapeutic interest in the context of cancer. We recently developed the pure antagonist Del1-9-G129R-hPRL by deleting the nine N-terminal residues of G129R-hPRL, a first generation partial antagonist. We determined the crystallographic structure of Del1-9-G129R-hPRL, which revealed no major change compared with wild type hPRL, indicating that its pure antagonistic properties are intrinsically due to the mutations. To decipher the molecular bases of pure antagonism, we compared the biological, physicochemical, and structural properties of numerous hPRL variants harboring N-terminal or Gly(129) mutations, alone or combined. The pure versus partial antagonistic properties of the multiple hPRL variants could not be correlated to differences in their affinities toward the hPRL receptor, especially at site 2 as determined by surface plasmon resonance. On the contrary, residual agonism of the hPRL variants was found to be inversely correlated to their thermodynamic stability, which was altered by all the Gly(129) mutations but not by those involving the N terminus. We therefore propose that residual agonism can be abolished either by further disrupting hormone site 2-receptor contacts by N-terminal deletion, as in Del1-9-G129R-hPRL, or by stabilizing hPRL and constraining its intrinsic flexibility, as in G129V-hPRL. 相似文献