114 research outputs found

    A Splicing Mutation in the Novel Mitochondrial Protein DNAJC11 Causes Motor Neuron Pathology Associated with Cristae Disorganization, and Lymphoid Abnormalities in Mice

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    Mitochondrial structure and function is emerging as a major contributor to neuromuscular disease, highlighting the need for the complete elucidation of the underlying molecular and pathophysiological mechanisms. Following a forward genetics approach with N-ethyl-N-nitrosourea (ENU)-mediated random mutagenesis, we identified a novel mouse model of autosomal recessive neuromuscular disease caused by a splice-site hypomorphic mutation in a novel gene of unknown function, DnaJC11. Recent findings have demonstrated that DNAJC11 protein co-immunoprecipitates with proteins of the mitochondrial contact site (MICOS) complex involved in the formation of mitochondrial cristae and cristae junctions. Homozygous mutant mice developed locomotion defects, muscle weakness, spasticity, limb tremor, leucopenia, thymic and splenic hypoplasia, general wasting and early lethality. Neuropathological analysis showed severe vacuolation of the motor neurons in the spinal cord, originating from dilatations of the endoplasmic reticulum and notably from mitochondria that had lost their proper inner membrane organization. The causal role of the identified mutation in DnaJC11 was verified in rescue experiments by overexpressing the human ortholog. The full length 63 kDa isoform of human DNAJC11 was shown to localize in the periphery of the mitochondrial outer membrane whereas putative additional isoforms displayed differential submitochondrial localization. Moreover, we showed that DNAJC11 is assembled in a high molecular weight complex, similarly to mitofilin and that downregulation of mitofilin or SAM50 affected the levels of DNAJC11 in HeLa cells. Our findings provide the first mouse mutant for a putative MICOS protein and establish a link between DNAJC11 and neuromuscular diseases

    Tool-support for Architecture Decision Documentation

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    The perspective of looking at software architecture as a set of architecture decisions is widely recognized in research. However, in practice architecture decisions are often not explicitly documented but reside in the architect’s mind as tacit knowledge or are only implicit in the models that the architect creates. Even though explicit capturing and documentation of architecture decisions has been associated with a multitude of benefits such as avoiding knowledge vaporization, supporting change impact estimation, increasing system understanding and knowledge sharing, and facilitating architecture evaluation. In cooperation with a large multinational industrial corporation, we developed a tool that should facilitate the documentation of architecture decisions, as there is currently no standardized decision documentation approach or tool that is suitable for company- wide use. The tool is an extension to Sparx Systems’ Enterprise Architect and is based on a theoretical framework comprised of five architectural viewpoints. The framework has been developed by the Software Engineering and Architecture group of the University of Groningen. We conducted an exploratory case study at our industry partner. The objective of this study was to assess the status quo of architecture decision documentation, to identify expectations of the ideal documentation approach, and to evaluate the advantages and limitations of the developed extension. The findings of the case-study suggest that the developed extension allows documenting decisions in a user-friendly way and provides valuable support to capture architecture decisions. However, we also identified important improvements, such as a clear separation of problem, outcome and alternatives within the used meta-model. The study also showed that decisions are receiving rising awareness but that a lack of tool-support and a lack of standard approach for ADD limit the documentation and the use of decisions in practice.
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