Development of an efficient regeneration system for bombarded calli from immature embryos of Moroccan durum wheat varieties

ArticleOne of the biggest obstacles limiting genetic transformation of durum wheat is the lack of an efficient regeneration system for bombarded tissues. Our study aims to optimize culture conditions for regenerating bombarded calli from immature embryos of four durum wheat varieties ‘Amria’, ‘Chaoui’, ‘Isly’ and ‘Marouane’, through comparing the effects of phytohormones (IAA, zeatin and their interaction) and nitrogen amount and sources on callus induction and plant regeneration. Both tested induction media induced approximately the same rate of induced calli for all the tested varieties. However, the interaction of the induction and the regeneration media showed a highly significant effect on plantlet regeneration for all tested varieties. After bombardment, IM1/RM2 combination proved to be the favourable medium with up to 200% and 120% plantlets regenerated for ‘Chaoui’ and ‘Isly’ varieties respectively. Encouraging results obtained in this study will help to promote the research in genetic transformation and its improvement

Mapping genetic determinants of host susceptibility to Pseudomonas aeruginosa lung infection in mice.

Background: P. aeruginosa is one of the top three causes of opportunistic human bacterial infections. The remarkable variability in the clinical outcomes of this infection is thought to be associated with genetic predisposition. However, the genes underlying host susceptibility to P. aeruginosa infection are still largely unknown. Results: As a step towards mapping these genes, we applied a genome wide linkage analysis approach to a mouse model. A large F2 intercross population, obtained by mating P. aeruginosa-resistant C3H/HeOuJ, and susceptible A/J mice, was used for quantitative trait locus (QTL) mapping. The F2 progenies were challenged with a P. aeruginosa clinical strain and monitored for the survival time up to 7 days post-infection, as a disease phenotype associated trait. Selected phenotypic extremes of the F2 distribution were genotyped with high-density single nucleotide polymorphic (SNP) markers, and subsequently QTL analysis was performed. A significant locus was mapped on chromosome 6 and was named P. aeruginosa infection resistance locus 1 (Pairl1). The most promising candidate genes, including Dok1, Tacr1, Cd207, Clec4f, Gp9, Gata2, Foxp1, are related to pathogen sensing, neutrophils and macrophages recruitment and inflammatory processes. Conclusions: We propose a set of genes involved in the pathogenesis of P. aeruginosa infection that may be explored to complement human studie

Marker-assisted introgression of Trypanotolerance QTL in mice

A marker-assisted introgression (MAI) experiment was conducted to use genetic markers to transfer each of the three trypanotolerance QTL from a donor mouse strain, C57BL/6, into a recipient mouse strain, A/J. We used a backcross strategy that consisted of selecting two lines, each carrying two of the donor QTL alleles through the backcross (BC) phase. At the fourth BC generation, single-carrier animals were selected for the production of homozygous animal in the intercross phase. The QTL regions (QTLR) were located on chromosomes MMU1, MMU5, and MMU17. Groups of mice with different genotypes and the parental lines were subjected to a challenge with Trypanosoma congolense. The results show that trypanotolerance QTL was successfully moved into the recipient background genotype, yielding a longer survival time. The mean estimated survival time was 57.9, 49.5, and 46.8 days for groups of mice carrying the donor QTL on MMU1, MMU5, and MMU17 on A/J background. The mean estimated survival time was 29.7 days for the susceptible A/J line and 68.8 days for the resistant C57BL/6 line. The estimated QTLR effects are close to 30% smaller than those in the original mapping population which was likely caused by the difference in the background on which the effects of QTLR are tested. This is the first report of successful marker-assisted introgression of QTL in animals. It is experimental proof of the use of genetic markers for marker-assisted introgression in animal breeding. Institut National des Recherches Agricoles du Bénin, 01 BP 884 COTONOU, République du Béni

Hepatic gene expression variations in response to high-fat diet-induced impaired glucose tolerance using RNAseq analysis in collaborative cross mouse population

Hepatic gene expression is known to differ between healthy and type 2 diabetes conditions. Identifying these variations will provide better knowledge to the development of gene-targeted therapies. The aim of this study is to assess diet-induced hepatic gene expression of susceptible versus resistant CC lines to T2D development. Next-generation RNA-sequencing was performed for 84 livers of diabetic and non-diabetic mice of 41 different CC lines (both sexes) following 12 weeks on high-fat diet (42% fat). Data analysis revealed significant variations of hepatic gene expression in diabetic versus non-diabetic mice with significant sex effect, where 601 genes were differentially expressed (DE) in overall population (males and females), 718 genes in female mice, and 599 genes in male mice. Top prioritized DE candidate genes were Lepr, Ins2, Mb, Ckm, Mrap2, and Ckmt2 for the overall population; for females-only group were Hdc, Serpina12, Socs1, Socs2, and Mb, while for males-only group were Serpine1, Mb, Ren1, Slc4a1, and Atp2a1. Data analysis for sex differences revealed 193 DE genes in health (Top: Lepr, Cav1, Socs2, Abcg2, and Col5a3), and 389 genes DE between diabetic females versus males (Top: Lepr, Clps, Ins2, Cav1, and Mrap2). Furthermore, integrating gene expression results with previously published QTL, we identified significant variants mapped at chromosomes at positions 36-49 Mb, 62-71 Mb, and 79-99 Mb, on chromosomes 9, 11, and 12, respectively. Our findings emphasize the complexity of T2D development and that significantly controlled by host complex genetic factors. As well, we demonstrate the significant sex differences between males and females during health and increasing to extent levels during disease/diabetes. Altogether, opening the venue for further studies targets the discovery of effective sex-specific and personalized preventions and therapies

Operational framework based on modeling languages to support product repository implementation.

Part 3: Tools and MethodologiesInternational audienceEmbracing Product Lifecycle Management approach involves integrating a product repository in the company information system. From customer's needs to disposal stage, several product representations exist. The product repository purpose is to secure consistency of one product representation with the others. This paper presents an operational modeling framework that supports product repository implementation. In order to ensure consistency, this framework identifies correspondences between entities of languages (“trade” languages and standard languages). The presented concepts are illustrated with correspondences between language entities of product designed and productplanned to be built Bills of Materials

Chasing the genes that control resistance to gastrointestinal nematodes

The host-protective immune response to infection with gastrointestinal (GI) nematodes involves a range of interacting processes that begin with recognition of the parasite’s antigens and culminate in an inflammatory reaction in the intestinal mucosa. Precisely which immune effectors are responsible for the loss of specific worms is still not known although many candidate effectors have beenproposed. However, it is now clear that many different genes regulate the response and that differences between hosts (fast or strong versus slow or weak responses) can be explained by allelic variation in crucial genes associated with the gene cascade that accompanies the immune response and/or genes encoding constitutively expressed receptor/signalling molecules. Major histocompatibility complex (MHC) genes have been recognized for some time as decisive in controlling immunity, and evidence that non-MHC genes are equally, if not more important in this respect has also been available for two decades. Nevertheless, whilst the former have been mapped in mice, only two candidate loci have been proposed for non-MHC genes and relatively little is known about their roles. Now, with the availability of microsatellite markers, it is possible to exploit linkage mapping techniques to identify quantitative trait loci (QTL) responsible for resistance to GI nematodes. Four QTL for resistance to Heligmosomoides polygyrus, and additional QTL affecting faecal egg production by the worms and the accompanying immune responses, have been identified. Fine mapping and eventually the identification of the genes (and their alleles) underlying QTL for resistance/susceptibility will permit informed searches for homologues in domestic animals, and human beings, through comparative genomic maps. This information in turn will facilitate targeted breeding to improve resistance in domestic animals and, in human beings, focused application of treatment and control strategies for GI nematodes

Interchain spacing and screening length modification of PSS backbone chains in zwitterion-doped poly(3,4-ethylenedioxythiophene):polystyrene sulfonate

The interchain spacing and screening length modification of deuterated PSS (d-PSS) backbone chains in zwitterion-doped PEDOT:d-PSS were studied as a function of the doping concentration using small angle neutron scattering. Results suggest that the dopant, 3-(N,N-Dimethylmyristylammonio)propanesulfonate (DYMAP), forms worm-like micelle structures in the PEDOT:d-PSS dispersion that grow in size as the doping concentration increases. The interchain spacing between negatively charged d-PSS remains unaffected by DYMAP up to 15 mM doping concentration. However, from 15 to 25 mM doping concentration, the interchain spacing increases due to steric interactions of grown DYMAP worm-like micelles with the d-PSS chains. At 30 mM doping concentration, the interchain distance between negatively charged d-PSS chains is reduced due to the gelation of the PEDOT:d-PSS dispersion caused by the crosslinking between long DYMAP worm-like micelles and d-PSS chains. Meanwhile, the screening length of the neutralized d-PSS segments attached to the PEDOT oligomers increases as the DYMAP concentration increases form 5 to 30 mM due to the neutralization of the negatively charged d-PSS segments by their Coulomb interaction with the cation in DYMAP

Novel Cardiac-Specific Biomarkers and the Cardiovascular Continuum

The concept of the cardiovascular continuum, introduced during the early 1990s, created a holistic view of the chain of events connecting cardiovascular-related risk factors with the progressive development of pathological-related tissue remodelling and ultimately, heart failure and death. Understanding of the tissue-specific changes, and new technologies developed over the last 25–30 years, enabled tissue remodelling events to be monitored in vivo and cardiovascular disease to be diagnosed more reliably than before. The tangible product of this evolution was the introduction of a number of biochemical markers such as troponin I and T, which are now commonly used in clinics to measure myocardial damage. However, biomarkers that can detect specific earlier stages of the cardiovascular continuum have yet to be generated and utilised. The majority of the existing markers are useful only in the end stages of the disease where few successful intervention options exist. Since a large number of patients experience a transient underlying developing pathology long before the signs or symptoms of cardiovascular disease become apparent, the requirement for new markers that can describe the early tissue-specific, matrix remodelling process which ultimately leads to disease is evident. This review highlights the importance of relating cardiac biochemical markers with specific time points along the cardiovascular continuum, especially during the early transient phase of pathology progression where none of the existing markers aid diagnosis

Molecular Engineering of Conjugated Polymers for Efficient Hole Transport and Defect Passivation in Perovskite Solar Cells

Organic-inorganic hybrid perovskite solar cells represent an exceptional candidate for nextgeneration photovoltaic technology. However, the presence of surface defects in perovskite crystals limits the performance as well as the stability of perovskite solar cells. We have employed a series of carbazole and benzothiadiazole (BT) based donor-acceptor copolymers, which have different lengths of alkoxy side-chains grafted on the BT unit, as the dopant-free hole transport materials (HTMs) for perovskite solar cells. We demonstrate that although these side-chains can reduce the π−π stacking structural order of these copolymers to affect the hole transport properties, the methoxy unit introduces a desired defect passivation effect. Compared to the Spiro-OMeTAD-based device, the copolymer with methoxy side-chains on the BT unit (namely PCDTBT1) as the HTM achieved superior power conversion efficiency and stability due to efficient hole transport and the suppression of trap-induced degradation, whilst the copolymer with octyloxy side-chains on the BT unit (namely PCDTBT8) as the HTM lead to poor performance and stability

Achieving over 11% power conversion efficiency in PffBT4T-2OD-based ternary polymer solar cells with enhanced open-circuit-voltage and suppressed charge recombination

© 2017 Elsevier Ltd Fabricating ternary solar cells (TSCs) is a promising strategy to improve the power conversion efficiency of organic photovoltaics without introducing sophisticated processing procedures. We report in this work high efficiency TSCs with the maximum PCE over 11% by introducing a medium band gap conjugated polymer PCDTBT8 into the PffBT4T-2OD:PC 71 BM binary photovoltaic system. Morphological investigation shows that the third component PCDTBT8 locates at the interface between PffBT4T-2OD and PC 71 BM without disrupting the crystallization of PffBT4T-2OD to maintain decent charge mobility, and loosens the fullerene aggregation networks to facilitate exciton dissociation. The efficient Förster energy transfer from PCDTBT8 to PffBT4T-2OD enables the ternary devices to retain a high short-circuit current density despite the slightly decreased light absorption. Device physics studies suggest that the addition of PCDTBT8 can enhance the built-in voltage, prolong the carrier lifetime, reduce the defect density and suppress the trap-assisted charge recombination, leading to an improved FF and V OC to enhance the efficiency of ternary devices