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Temporary adhesion of the proseriate flatworm Minona ileanae

机译:突出突出虫Minona Ileanae的临时粘附

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摘要

Flatworms can very rapidly attach to and detach from many substrates. In the presented work, we analysed the adhesive system of the marine proseriate flatworm Minona ileanae. We used light-, scanning- and transmission electron microscopy to analyse the morphology of the adhesive organs, which are located at the ventral side of the tail-plate. We performed transcriptome sequencing and differential RNA-seq for the identification of tail-specific transcripts. Using in situ hybridization expression screening, we identified nine transcripts that were expressed in the cells of the adhesive organs. Knock-down of five of these transcripts by RNA interference led to a reduction of the animal's attachment capacity. Adhesive proteins in footprints were confirmed using mass spearometry and antibody staining. Additionally, lectin labelling of footprints revealed the presence of several sugar moieties. Furthermore, we determined a genome size of about 560 Mb for M. ileanae. We demonstrated the potential of Oxford Nanopore sequencing of genomic DNA as a cost-effective tool for identifying the number of repeats within an adhesive protein and for combining transcripts that were fragments of larger genes. A better understanding of the molecules involved in flatworm bioadhesion can pave the way towards developing innovative glues with reversible adhesive properties.
机译:扁虫可以非常迅速地附着在许多基板上并分离。在本工作中,我们分析了海洋潜水虫Minona Ileanae的粘合剂系统。我们使用了光,扫描和透射电子显微镜,分析了位于尾板的腹侧的粘合器官的形态。我们进行转录组测序和差分RNA-SEQ,用于鉴定特定的尾部转录物。使用原位杂交表达筛选,我们鉴定了在粘合器官的细胞中表达的九转会。通过RNA干扰击落其中五种转录物的下降导致动物的附着力的减少。使用质量芯片测量和抗体染色确认粘合剂蛋白。此外,侧胶标记的占地面积显示出几种糖部分的存在。此外,我们确定了M. Ileanae约560mb的基因组大小。我们证明了基因组DNA的牛津纳米孔测序的潜力作为用于鉴定粘合剂蛋白内的重复数量的成本效益的工具,并将转录物组合为较大基因片段的转录物。更好地了解涉及扁虫生物粘面的分子可以促使朝向开发具有可逆粘合性能的创新胶水。

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