23 research outputs found
Corporate governance for sustainability : Statement
The current model of corporate governance needs reform. There is mounting evidence that the practices of shareholder primacy drive company directors and executives to adopt the same short time horizon as financial markets. Pressure to meet the demands of the financial markets drives stock buybacks, excessive dividends and a failure to invest in productive capabilities. The result is a ‘tragedy of the horizon’, with corporations and their shareholders failing to consider environmental, social or even their own, long-term, economic sustainability.
With less than a decade left to address the threat of climate change, and with consensus emerging that businesses need to be held accountable for their contribution, it is time to act and reform corporate governance in the EU.
The statement puts forward specific recommendations to clarify the obligations of company boards and directors and make corporate governance practice significantly more sustainable and focused on the long term
Host-pathogen relationship of geographically diverse isolates of Septoria tritici and wheat cultivars
Response of Schoenoplectus acutus and Schoenoplectus californicus at Different Life-History Stages to Hydrologic Regime
Nucleosomes can invade DNA territories occupied by their neighbors
Nucleosomes are the fundamental subunits of eukaryotic chromatin. They are not static entities, but can undergo a number of dynamic transitions including spontaneous repositioning along DNA. Since nucleosomes are spaced close together within genomes it is likely that on occasion they approach each other and or collide. Here we have used a dinucleosomal model system to show that the 147bp DNA territories of two nucleosomes can overlap extensively. In the situation of an overlap by 44 bp or 54 bp one histone dimer is lost and the resulting complex can condense to form a compact single particle. We propose a pathway in which adjacent nucleosomes promote DNA unraveling as they approach each other and that this permits their 147bp territories to overlap. These may represent early steps in a pathway for nucleosome removal via collision. In eukaryotic cells genomic DNA exists in the form of a nucleo-protein complex called chromatin 1. The packaging of the genomic DNA imposes a hindrance to most DNA-dependent processes including DNA replication, repair and mRNA transcription. This implies an important role for chromatin structure in the control of many nuclear functions 2,3. The first step in the packaging hierarchy of chromatin is the formation of a nucleosom
Metazoan parasites of Plagioscion squamosissimus, an invasive species in the Tietê River, São Paulo, Brazil
Coastal plain forests in southern and southeastern Brazil: ecological drivers, floristic patterns and conservation status
Missing heritability: Is the gap closing? An analysis of 32 complex traits in the LifeLines Cohort Study
Despite the recent explosive rise in number of genetic markers for complex disease traits identified in genome-wide association studies, there is still a large gap between the known heritability of these traits and the part explained by these markers. To gauge whether this 'heritability gap' is closing, we first identified genome-wide significant SNPs from the literature and performed replication analyses for 32 highly relevant traits from five broad disease areas in 13 436 subjects of the Lifelines Cohort. Next, we calculated the variance explained by multi-SNP genetic risk scores (GRSs) for each trait, and compared it to their broad-and narrow-sense heritabilities captured by all common SNPs. The majority of all previously-associated SNPs (median = 75%) were significantly associated with their respective traits. All GRSs were significant, with unweighted GRSs generally explaining less phenotypic variance than weighted GRSs, for which the explained variance was highest for height (15.5%) and varied between 0.02 and 6.7% for the other traits. Broad-sense common-SNP heritability estimates were significant for all traits, with the additive effect of common SNPs explaining 48.9% of the variance for height and between 5.6 and 39.2% for the other traits. Dominance effects were uniformly small (0-1.5%) and not significant. On average, the variance explained by the weighted GRSs accounted for only 10.7% of the common-SNP heritability of the 32 traits. These results indicate that GRSs may not yet be ready for accurate personalized prediction of complex disease traits limiting widespread adoption in clinical practice