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Targeted Mutagenesis in Atlantic Salmon (Salmo salar L.) Using the CRISPR/Cas9 System Induces Complete Knockout Individuals in the F0 Generation

机译:使用CRISPR / Cas9系统在大西洋鲑鱼(Salmo salar L.)中进行定向诱变诱导F0代中的完全敲除个体

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摘要

Understanding the biological function behind key proteins is of great concern in Atlantic salmon, both due to a high commercial importance and an interesting life history. Until recently, functional studies in salmonids appeared to be difficult. However, the recent discovery of targeted mutagenesis using the CRISPR/Cas9 (clustered regularly interspaced palindromic repeats/CRISPR-associated) system enables performing functional studies in Atlantic salmon to a great extent. We used the CRISPR/Cas9 system to target two genes involved in pigmentation, tyrosinase (tyr) and solute carrier family 45, member 2 (slc45a2). Embryos were assayed for mutation rates at the 17 somite stage, where 40 and 22% of all injected embryos showed a high degree of mutation induction for slc45a2 and tyr, respectively. At hatching this mutation frequency was also visible for both targeted genes, displaying a graded phenotype ranging from complete lack of pigmentation to partial loss and normal pigmentation. CRISPRslc45a2/Cas9 injected embryos showing a complete lack of pigmentation or just a few spots of pigments also lacked wild type sequences when assaying more than 80 (slc45a2) sequence clones from whole embryos. This indicates that CRISPR/Cas9 can induce double-allelic knockout in the F0 generation. However, types and frequency of indels might affect the phenotype. Therefore, the variation of indels was assayed in the graded pigmentation phenotypes produced by CRISPR/Cas9-slc45a2. The results show a tendency for fewer types of indels formed in juveniles completely lacking pigmentation compared to juveniles displaying partial pigmentation. Another interesting observation was a high degree of the same indel type in different juveniles. This study shows for the first time successful use of the CRISPR/Cas9 technology in a marine cold water species. Targeted double-allelic mutations were obtained and, though the level of mosaicism has to be considered, we demonstrate that F0 fish can be used for functional studies in Atlantic salmon.
机译:由于高度的商业重要性和有趣的生活历史,了解关键蛋白背后的生物学功能是大西洋鲑非常关注的问题。直到最近,鲑鱼的功能研究似乎还很困难。然而,最近发现的使用CRISPR / Cas9(成簇的规则间隔的回文重复序列/ CRISPR关联的)系统进行定向诱变的研究使得能够在很大程度上进行大西洋鲑鱼的功能研究。我们使用CRISPR / Cas9系统靶向涉及色素沉着的两个基因,酪氨酸酶(tyr)和溶质载体家族45,成员2(slc45a2)。分析了胚胎在17个体节阶段的突变率,其中所有注射的胚胎中40%和22%分别对slc45a2和tyr表现出高度的突变诱导。孵化时,这两个靶基因的突变频率也是可见的,表现出从完全缺乏色素沉着到部分丢失和正常色素沉着的分级表型。当从整个胚胎中分析80多个(slc45a2)序列克隆时,CRISPRslc45a2 / Cas9注射的胚胎显示出完全没有色素沉着或只有少量色素也缺乏野生型序列。这表明CRISPR / Cas9可以在F0代中诱导双等位基因敲除。但是,插入缺失的类型和频率可能会影响表型。因此,在由CRISPR / Cas9-slc45a2产生的分级色素沉着表型中测定了插入缺失的变化。结果表明,与显示部分色素沉着的少年相比,在完全缺乏色素沉着的少年中形成更少类型的插入缺失的趋势。另一个有趣的发现是在不同的青少年中高度相同的插入/缺失类型。这项研究首次显示了CRISPR / Cas9技术在海洋冷水物种中的成功使用。获得了有针对性的双等位基因突变,尽管必须考虑镶嵌水平,但我们证明F0鱼可用于大西洋鲑鱼的功能研究。

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