63 research outputs found
Localization of protamine 1 mRNA in different stages of the cycle of the rat seminiferous epithelium.
HSPG-Deficient Zebrafish Uncovers Dental Aspect of Multiple Osteochondromas
Multiple Osteochondromas (MO; previously known as multiple hereditary exostosis) is an autosomal dominant genetic condition that is characterized by the formation of cartilaginous bone tumours (osteochondromas) at multiple sites in the skeleton, secondary bursa formation and impingement of nerves, tendons and vessels, bone curving, and short stature. MO is also known to be associated with arthritis, general pain, scarring and occasional malignant transformation of osteochondroma into secondary peripheral chondrosarcoma. MO patients present additional complains but the relevance of those in relation to the syndromal background needs validation. Mutations in two enzymes that are required during heparan sulphate synthesis (EXT1 or EXT2) are known to cause MO. Previously, we have used zebrafish which harbour mutations in ext2 as a model for MO and shown that ext2−/− fish have skeletal defects that resemble those seen in osteochondromas. Here we analyse dental defects present in ext2−/− fish. Histological analysis reveals that ext2−/− fish have very severe defects associated with the formation and the morphology of teeth. At 5 days post fertilization 100% of ext2−/− fish have a single tooth at the end of the 5th pharyngeal arch, whereas wild-type fish develop three teeth, located in the middle of the pharyngeal arch. ext2−/− teeth have abnormal morphology (they were shorter and thicker than in the WT) and patchy ossification at the tooth base. Deformities such as split crowns and enamel lesions were found in 20% of ext2+/− adults. The tooth morphology in ext2−/− was partially rescued by FGF8 administered locally (bead implants). Our findings from zebrafish model were validated in a dental survey that was conducted with assistance of the MHE Research Foundation. The presence of the malformed and/or displaced teeth with abnormal enamel was declared by half of the respondents indicating that MO might indeed be also associated with dental problems
Surface properties changing of biodegradable polymers by the radio frequency magnetron sputtering modification
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A transgenic resource for conditional competitive inhibition of conserved Drosophila microRNAs
Although the impact of microRNAs (miRNAs) in development and disease is well established, understanding the function of individual miRNAs remains challenging. Development of competitive inhibitor molecules such as miRNA sponges has allowed the community to address individual miRNA function in vivo. However, the application of these loss-of-function strategies has been limited. Here we offer a comprehensive library of 141 conditional miRNA sponges targeting well-conserved miRNAs in Drosophila. Ubiquitous miRNA sponge delivery and consequent systemic miRNA inhibition uncovers a relatively small number of miRNA families underlying viability and gross morphogenesis, with false discovery rates in the 4–8% range. In contrast, tissue-specific silencing of muscle-enriched miRNAs reveals a surprisingly large number of novel miRNA contributions to the maintenance of adult indirect flight muscle structure and function. A strong correlation between miRNA abundance and physiological relevance is not observed, underscoring the importance of unbiased screens when assessing the contributions of miRNAs to complex biological processes
A whole-genome shotgun approach for assembling and anchoring the hexaploid bread wheat genome
Citation: Chapman, J. A., Mascher, M., Buluç, A., Barry, K., Georganas, E., Session, A., . . . Rokhsar, D. S. (2015). A whole-genome shotgun approach for assembling and anchoring the hexaploid bread wheat genome. Genome Biology, 16(1). doi:10.1186/s13059-015-0582-8Polyploid species have long been thought to be recalcitrant to whole-genome assembly. By combining high-throughput sequencing, recent developments in parallel computing, and genetic mapping, we derive, de novo, a sequence assembly representing 9.1 Gbp of the highly repetitive 16 Gbp genome of hexaploid wheat, Triticum aestivum, and assign 7.1 Gb of this assembly to chromosomal locations. The genome representation and accuracy of our assembly is comparable or even exceeds that of a chromosome-by-chromosome shotgun assembly. Our assembly and mapping strategy uses only short read sequencing technology and is applicable to any species where it is possible to construct a mapping population. © 2015 Chapman et al. licensee BioMed Central.Additional Authors: Muehlbauer, G. J.;Stein, N.;Rokhsar, D. S
Building and Combining Matching Algorithms
International audienceThe concept of matching is ubiquitous in declarative programming and in automated reasoning. For instance, it is a key mechanism to run rule-based programs and to simplify clauses generated by theorem provers. A matching problem can be seen as a particular conjunction of equations where each equation has a ground side. We give an overview of techniques that can be applied to build and combine matching algorithms. First, we survey mutation-based techniques as a way to build a generic matching algorithm for a large class of equational theories. Second, combination techniques are introduced to get combined matching algorithms for disjoint unions of theories. Then we show how these combination algorithms can be extended to handle non-disjoint unions of theories sharing only constructors. These extensions are possible if an appropriate notion of normal form is computable
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A Performance Analysis of the Berkeley UPC Compiler
Unified Parallel C (UPC) is a parallel language that uses a Single Program Multiple Data (SPMD) model of parallelism within a global address space. The global address space is used to simplify programming, especially on applications with irregular data structures that lead to fine-grained sharing between threads. Recent results have shown that the performance of UPC using a commercial compiler is comparable to that of MPI [7]. In this paper we describe a portable open source compiler for UPC. Our goal is to achieve a similar performance while enabling easy porting of the compiler and runtime, and also provide a framework that allows for extensive optimizations. We identify some of the challenges in compiling UPC and use a combination of micro-benchmarks and application kernels to show that our compiler has low overhead for basic operations on shared data and is competitive, and sometimes faster than, the commercial HP compiler. We also investigate several communication optimizations, and show significant benefits by hand-optimizing the generated code
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Integration and evolution of the cichlid mandible: The molecular basis of alternate feeding strategies
African cichlid fishes have repeatedly evolved highly specialized modes of feeding through adaptations of their oral jaws. Here, we explore the molecular genetic basis of the opening and closing lever mechanisms of the cichlid lower jaw, which have traditionally been used to describe the mechanics of feeding behavior in bony fishes. Quantitative genetic analyses demonstrate that the opening and closing mechanisms are genetically modular and therefore free to evolve independently. Bmp4 (bone morphogenetic protein 4) is one of two loci that segregate with the mechanical advantage of closing and that together account for \u3e30% of the phenotypic variance in this trait. Species-specific differences in jaw shape are obvious early in cichlid larval development and are correlated with patterns of bmp4 expression in the mandibular primordium. When bmp4 is overexpressed in the obligate suction feeder Danio rerio, mandibular morphology exhibits specific transformations of opening and closing lever ratios. We conclude that patterns of morphological integration of the cichlid jaw reflect a balance among conflicting functional demands. Further, we demonstrate that bmp4 has the potential to alter mandibular morphology in a way that mimics adaptive variation among fish species
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