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Turning gene function ON and OFF using sense and antisense photo-morpholinos in zebrafish

机译:使用有义和反义光吗啉代打开和关闭斑马鱼的基因功能

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To understand the molecular mechanisms of development it is essential to be able to turn genes on and off at will and in a spatially restricted fashion. Morpholino oligonucleotides (MOs) are very common tools used in several model organisms with which it is possible to block gene expression. Recently developed photo-activated MOs allow control over the onset of MO activity. However, deactivation of photo-cleavable MO activity has remained elusive. Here, we describe photo-cleavable MOs with which it is possible to activate or de-activate MO function by UV exposure in a temporal and spatial manner. We show, using several different genes as examples, that it is possible to turn gene expression on or off both in the entire zebrafish embryo and in single cells. We use these tools to demonstrate the sufficiency of no tail expression as late as tailbud stage to drive medial precursor cells towards the notochord cell fate. As a broader approach for the use of photo-cleavable MOs, we show temporal control over gal4 function, which has many potential applications in multiple transgenic lines. We demonstrate temporal manipulation of Gal4 transgene expression in only primary motoneurons and not secondary motoneurons, heretofore impossible with conventional transgenic approaches. In another example, we follow and analyze neural crest cells that regained sox10 function after deactivation of a photo-cleavable sox10-MO at different time points. Our results suggest that sox10 function might not be critical during neural crest formation.
机译:要了解发育的分子机制,至关重要的是能够随意并以空间受限的方式打开和关闭基因。吗啉代寡核苷酸(MOs)是在几种模式生物中使用的非常普遍的工具,可用来阻断基因表达。最近开发的光活化MO允许控制MO活性的发作。然而,光可裂解MO活性的失活仍然难以实现。在这里,我们描述了光可裂解的MO,利用它们可以通过时间和空间上的紫外线暴露来激活或去激活MO功能。我们以几个不同的基因为例表明,有可能在整个斑马鱼胚胎和单个细胞中打开或关闭基因表达。我们使用这些工具来证明没有尾巴表达,直到尾巴阶段就足以驱动内侧前体细胞趋向脊索细胞命运。作为使用光可裂解MO的更广泛方法,我们显示了对gal4功能的时间控制,该功能在多个转基因品系中具有许多潜在应用。我们证明Gal4转基因表达的暂时操纵仅在主要的运动神经元中,而不在次要的运动神经元中,这是常规转基因方法迄今不可能的。在另一个示例中,我们跟踪并分析了在不同时间点光裂解的sox10-MO失活后恢复了sox10功能的神经c细胞。我们的结果表明,sox10功能在神经c形成过程中可能并不关键。

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