51 research outputs found

    Patterns and roles of lignan and terpenoid accumulation in the reaction zone compartmentalizing pathogen-infected heartwood of Norway spruce

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    Tree defense against xylem pathogens involves both constitutive and induced phenylpropanoids and terpenoids. The induced defenses include compartmentalization of compromised wood with a reaction zone (RZ) characterized by polyphenol deposition, whereas the role of terpenoids has remained poorly understood. To further elucidate the tree–pathogen interaction, we profiled spatial patterns in lignan (low-molecular-weight polyphenols) and terpenoid content in Norway spruce (Picea abies) trees showing heartwood colonization by the pathogenic white-rot fungus Heterobasidion parviporum. There was pronounced variation in the amount and composition of lignans between different xylem tissue zones of diseased and healthy trees. Intact RZ at basal stem regions, where colonization is the oldest, showed the highest level and diversity of these compounds. The antioxidant properties of lignans obviously hinder oxidative degradation of wood: RZ with lignans removed by extraction showed significantly higher mass loss than unextracted RZ when subjected to Fenton degradation. The reduced diversity and amount of lignans in pathogen-compromised RZ and decaying heartwood in comparison to intact RZ and healthy heartwood suggest that α-conindendrin isomer is an intermediate metabolite in lignan decomposition by H. parviporum. Diterpenes and diterpene alcohols constituted above 90% of the terpenes detected in sapwood of healthy and diseased trees. A significant finding was that traumatic resin canals, predominated by monoterpenes, were commonly associated with RZ. The findings clarify the roles and fate of lignan during wood decay and raise questions about the potential roles of terpenoids in signal transduction, synthesis, and translocation of defense compounds upon wood compartmentalization against decay fungi.publishedVersio

    Collaborative development of predictive toxicology applications

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    OpenTox provides an interoperable, standards-based Framework for the support of predictive toxicology data management, algorithms, modelling, validation and reporting. It is relevant to satisfying the chemical safety assessment requirements of the REACH legislation as it supports access to experimental data, (Quantitative) Structure-Activity Relationship models, and toxicological information through an integrating platform that adheres to regulatory requirements and OECD validation principles. Initial research defined the essential components of the Framework including the approach to data access, schema and management, use of controlled vocabularies and ontologies, architecture, web service and communications protocols, and selection and integration of algorithms for predictive modelling. OpenTox provides end-user oriented tools to non-computational specialists, risk assessors, and toxicological experts in addition to Application Programming Interfaces (APIs) for developers of new applications. OpenTox actively supports public standards for data representation, interfaces, vocabularies and ontologies, Open Source approaches to core platform components, and community-based collaboration approaches, so as to progress system interoperability goals

    Finishing the euchromatic sequence of the human genome

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    The sequence of the human genome encodes the genetic instructions for human physiology, as well as rich information about human evolution. In 2001, the International Human Genome Sequencing Consortium reported a draft sequence of the euchromatic portion of the human genome. Since then, the international collaboration has worked to convert this draft into a genome sequence with high accuracy and nearly complete coverage. Here, we report the result of this finishing process. The current genome sequence (Build 35) contains 2.85 billion nucleotides interrupted by only 341 gaps. It covers ∼99% of the euchromatic genome and is accurate to an error rate of ∼1 event per 100,000 bases. Many of the remaining euchromatic gaps are associated with segmental duplications and will require focused work with new methods. The near-complete sequence, the first for a vertebrate, greatly improves the precision of biological analyses of the human genome including studies of gene number, birth and death. Notably, the human enome seems to encode only 20,000-25,000 protein-coding genes. The genome sequence reported here should serve as a firm foundation for biomedical research in the decades ahead

    The relationship of family factors and psychiatric symptoms in patients with bipolar disorder

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    Expressed Emotion (EE), Affective Style (AS), and Coping Style (CS) as measures of the intrafamilial environment have been shown to be predictive of outcome in a variety of psychiatric and physical disorders, as well as across several different cultures. In addition, strong interrelationships have been found between all of these variables, most particularly with schizophrenic patients and their biological relatives. The present investigation sought to examine the interrelationships between EE, AS, and CS in a sample of 38 bipolar patients and their spouses. In addition, the relationships between these three variables and marital distress in each of the pair, Axis I illness in the spouse, and Axis II pathology in each member of the couple was assessed. A significant relationship was found between EE and AS, indicating that critical attitudes held by the spouse were reflected in interactional exchanges with their patient partner. Patient and spouse marital distress was found to be correlated with both EE and AS. This indicates that marital distress in each of the pair is related to the critical attitudes which the spouse holds with respect to the patient, and how critical or disparaging the patient is in direct interaction with their mate. None of the other analyses produced significant results. There are several factors which may inhibit the interpretation and the generalizability of the results. First, as the analyses used were correlational in nature, causality cannot be inferred. Second, this group of patients was considerably older, with a longer duration of illness than other research samples. Third, the sample size was somewhat small. Future research should focus an determining more precisely the actual correlates of EE, AS, and CS. In addition, sequential analyses of the interactional exchanges between family members would help to clarify what actually occurs during these critical interchanges. Finally, as the relationship between EE, AS, and CS and marital distress is a relatively unique finding, it would be interesting for future studies to try to explore this relationship more thoroughly
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