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在赤拟谷盗中生成并测试转基因Cas9的功效。

Generating and testing the efficacy of transgenic Cas9 in Tribolium castaneum.

作者信息

Rylee Johnathan C, Nin-Velez Alexandra, Mahato Simpla, Helms Kennedy J, Wade Michael J, Zentner Gabriel E, Zelhof Andrew C

机构信息

Department of Biology, Indiana University, Bloomington, Indiana, USA.

出版信息

Insect Mol Biol. 2022 Oct;31(5):543-550. doi: 10.1111/imb.12778. Epub 2022 Apr 25.

Abstract

CRISPR/Cas9 genome editing has now expanded to many insect species, including Tribolium castaneum. However, compared to Drosophila melanogaster, the CRISPR toolkit of T. castaneum is limited. A particularly apparent gap is the lack of Cas9 transgenic animals, which generally offer higher editing efficiency. We address this by creating and testing transgenic beetles expressing Cas9. We generated two different constructs bearing basal heat shock promoter-driven Cas9, two distinct 3' UTRs, and one containing Cas9 fused to EGFP by a T2A peptide. Analyses of Cas9 activity in each transgenic line demonstrated that both designs are capable of inducing CRISPR- mediated changes in the genome in the absence of heat induction. Overall, these resources enhance the accessibility of CRISPR/Cas9 genome editing for the Tribolium research community and provide a benchmark against which to compare future transgenic Cas9 lines.

摘要

CRISPR/Cas9基因组编辑技术现已扩展到包括赤拟谷盗在内的许多昆虫物种。然而,与黑腹果蝇相比,赤拟谷盗的CRISPR工具包较为有限。一个特别明显的差距是缺乏Cas9转基因动物,而这类动物通常具有更高的编辑效率。我们通过创建和测试表达Cas9的转基因甲虫来解决这个问题。我们构建了两种不同的载体,一种带有基础热休克启动子驱动的Cas9、两种不同的3'非翻译区,另一种含有通过T2A肽与EGFP融合的Cas9。对每个转基因品系中Cas9活性的分析表明,两种设计在没有热诱导的情况下都能够诱导基因组中CRISPR介导的变化。总体而言,这些资源提高了赤拟谷盗研究群体对CRISPR/Cas9基因组编辑的可及性,并提供了一个基准,可用于比较未来的转基因Cas9品系。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4290/9544626/6921ee6fc87a/IMB-31-543-g003.jpg

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