287 research outputs found

    Seedling development traits in Brassica napus examined by gene expression analysis and association mapping

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    BACKGROUND: An optimal seedling development of Brassica napus plants leads to a higher yield stability even under suboptimal growing conditions and has therefore a high importance for plant breeders. The objectives of our study were to (i) examine the expression levels of candidate genes in seedling leaves of B. napus and correlate these with seedling development as well as (ii) detect genome regions associated with gene expression levels and seedling development traits in B. napus by genome-wide association mapping. RESULTS: The expression levels of the 15 candidate genes examined in the 509 B. napus inbreds showed an averaged standard deviation of 5.6 across all inbreds and ranged from 3.2 to 8.8. The gene expression differences between the 509 B. napus inbreds were more than adequate for the correlation with phenotypic variation of seedling development. The average of the absolute value correlations of the correlation coefficients of 0.11 were observed with a range from 0.00 to 0.39. The candidate genes GER1, AILP1, PECT, and FBP were strongly correlated with the seedling development traits. In a genome-wide association study, we detected a total of 63 associations between single nucleotide polymorphisms (SNPs) and the seedling development traits and 31 SNP-gene associations for the candidate genes with a P-value < 0.0001. For the projected leaf area traits we identified five different association hot spots on the chromosomes A2, A7, C3, C6, and C7. CONCLUSION: A total of 99.4% of the adjacent SNPs on the A genome and 93.0% of the adjacent SNPs on the C genome had a distance smaller than the average range of linkage disequilibrium. Therefore, this genome-wide association study is expected to result on average in 14.7% of the possible power. Compared to previous studies in B. napus, the SNP marker density of our study is expected to provide a higher power to detect SNP-trait/-gene associations in the B. napus diversity set. The large number of associations detected for the examined 14 seedling development traits indicated that these are genetically complex inherited. The results of our analyses suggested that the studied genes ribulose 1,5-bisphosphate carboxylase/oxygenase small subunit (RBC) on the chromosomes A4 and C4 and fructose-1,6-bisphosphatase precursor (FBP) on the chromosomes A9 and C8 are cis-regulated. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12870-015-0496-3) contains supplementary material, which is available to authorized users

    Transparent Conducting Oxides for Photovoltaics: Manipulation of Fermi Level, Work Function and Energy Band Alignment

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    Doping limits, band gaps, work functions and energy band alignments of undoped and donor-doped transparent conducting oxides Zn₀, In₂O₃, and SnO₂ as accessed by X-ray and ultraviolet photoelectron spectroscopy (XPS/UPS) are summarized and compared. The presented collection provides an extensive data set of technologically relevant electronic properties of photovoltaic transparent electrode materials and illustrates how these relate to the underlying defect chemistry, the dependence of surface dipoles on crystallographic orientation and/or surface termination, and Fermi level pinning

    Quasiparticle spin susceptibility in heavy-fermion superconductors : An NMR study compared with specific heat results

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    Quasi-particle spin susceptibility (χqp\chi^{qp}) for various heavy-fermion (HF) superconductors are discussed on the basis of the experimental results of electronic specific heat (γel\gamma_{el}), NMR Knight shift (KK) and NMR relaxation rate (1/T11/T_1) within the framework of the Fermi liquid model for a Kramers doublet crystal electric field (CEF) ground state. χγqp\chi^{qp}_{\gamma} is calculated from the enhanced Sommerfeld coefficient γel\gamma_{el} and χT1qp\chi^{qp}_{T_1} from the quasi-particle Korringa relation T1T(KT1qp)2=const.T_1T(K^{qp}_{T_1})^2=const. via the relation of χT1qp=(NAμB/Ahf)KT1qp\chi^{qp}_{T_1}=(N_A\mu_B/A_{hf})K^{qp}_{T_1} where AhfA_{hf} is the hyperfine coupling constant, NAN_A the Abogadoro's number and μB\mu_B the Bohr magneton. For the even-parity (spin-singlet) superconductors CeCu2_2Si2_2, CeCoIn5_5 and UPd2_2Al3_3, the fractional decrease in the Knight shift, δKobs\delta K^{obs}, below the superconducting transition temperature (TcT_c) is due to the decrease of the spin susceptibility of heavy quasi-particle estimated consistently from χγqp\chi^{qp}_{\gamma} and χT1qp\chi^{qp}_{T_1}. This result allows us to conclude that the heavy quasi-particles form the spin-singlet Cooper pairs in CeCu2_2Si2_2, CeCoIn5_5 and UPd2_2Al3_3. On the other hand, no reduction in the Knight shift is observed in UPt3_3 and UNi2_2Al3_3, nevertheless the estimated values of χγqp\chi^{qp}_{\gamma} and χT1qp\chi^{qp}_{T_1} are large enough to be probed experimentally. The odd-parity superconductivity is therefore concluded in these compounds. The NMR result provides a convincing way to classify the HF superconductors into either even- or odd- parity paring together with the identification for the gap structure, as long as the system has Kramers degeneracy.Comment: 11 pages, 3 tables, 5 figures, RevTex4(LaTex2e

    Genetic and antigenic characterization of complete genomes of Type 1 Porcine Reproductive and Respiratory Syndrome viruses (PRRSV) isolated in Denmark over a period of 10 years

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    AbstractPorcine Reproductive and Respiratory Syndrome (PRRS) caused by the PRRS virus (PRRSV) is considered one of the most devastating swine diseases worldwide. PRRS viruses are divided into two major genotypes, Type 1 and Type 2, with pronounced diversity between and within the genotypes. In Denmark more than 50% of the herds are infected with Type 1 and/or Type 2 PRRSV. The main objective of this study was to examine the genetic diversity and drift of Type 1 viruses in a population with limited introduction of new animals and semen. A total of 43 ORF5 and 42 ORF7 nucleotide sequences were obtained from viruses collected from 2003 to February 2013. Phylogenetic analysis of ORF5 nucleotide sequences showed that the Danish isolates formed two major clusters within the subtype 1. The nucleotide identity to the subtype 1 protogenotype Lelystad virus (LV) spanned 84.9–98.8% for ORF5 and 90.7–100% for ORF7. Among the Danish viruses the pairwise nucleotide identities in ORF5 and ORF7 were 81.2–100% and 88.9–100%, respectively. Sequencing of the complete genomes, including the 5′- and 3′-end nucleotides, of 8 Danish PRRSV Type 1 showed that the genome lengths differed from 14,876 to 15,098 nucleotides and the pairwise nucleotide identity among the Danish viruses was 86.5–97.3% and the identity to LV was 88.7–97.9%. The study strongly indicated that there have been at least two independent introductions of Type 1 PRRSV in Denmark and analysis of the full genomes revealed a significant drift in several regions of the virus
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