CRISPR/Cas9介导的非模式线虫PS1159的基因编辑

IF 4.9 Q1 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Viktoria Hellekes, Denise Claus, Johanna Seiler, Felix Illner, Philipp H Schiffer, Michael Kroiher
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引用次数: 3

摘要

线虫门在广泛的生态系统和栖息地中拥有巨大的物种多样性。线虫在很大程度上共享保守的包氏计划,但在早期发育过程中发现了重大差异。几十年来,人们对线虫模式生物秀丽隐杆线虫的发育进行了详细的研究。这些努力为社区提供了大量的协议和方法。不幸的是,许多这些工具不容易适用于非隐杆线虫。近年来,人们发现秀丽隐杆线虫发育工具箱中的许多关键基因在其他线虫物种中是缺失的。因此,有必要详细研究其他线虫物种的发育过程,以了解该门的进化保守性和新颖性。Panagrolaimus sp. PS1159是一种单性生殖的非寄生线虫,我们正在建立该物种,以比较研究其进化、生物多样性和替代繁殖和生存策略。本研究首次成功地将CRISPR/Cas9系统应用于Panagrolaimus sp. PS1159和与其密切相关的两性物种Propanagrolaimus sp. JU765的基因组编辑,应用了非同源末端连接和同源定向修复(homology-directed repair, HDR)机制。通过显微注射和修改已发表的秀丽隐杆线虫和太平洋p.a ificus的方案,我们诱导了unc-22同源物的突变。这导致了一个可见的不协调抽搐表型。我们还比较了不同单链寡脱氧核苷酸(ssODNs)递送后的HDR效率。我们的工作将扩大对非模式线虫的适用性,并促进对单性生殖进化、线虫发育程序变化和隐生的功能分析。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

CRISPR/Cas9 mediated gene editing in non-model nematode <i>Panagrolaimus</i> sp. PS1159.

CRISPR/Cas9 mediated gene editing in non-model nematode <i>Panagrolaimus</i> sp. PS1159.

CRISPR/Cas9 mediated gene editing in non-model nematode <i>Panagrolaimus</i> sp. PS1159.

CRISPR/Cas9 mediated gene editing in non-model nematode Panagrolaimus sp. PS1159.

The phylum Nematoda harbors a huge diversity of species in a broad range of ecosystems and habitats. Nematodes share a largely conserved Bauplan but major differences have been found in early developmental processes. The development of the nematode model organism Caenorhabditis elegans has been studied in great detail for decades. These efforts have provided the community with a large number of protocols and methods. Unfortunately, many of these tools are not easily applicable in non-Caenorhabditis nematodes. In recent years it has become clear that many crucial genes in the C. elegans developmental toolkit are absent in other nematode species. It is thus necessary to study the developmental program of other nematode species in detail to understand evolutionary conservation and novelty in the phylum. Panagrolaimus sp. PS1159 is a non-parasitic nematode exhibiting parthenogenetic reproduction and we are establishing the species to comparatively study evolution, biodiversity, and alternative reproduction and survival strategies. Here, we demonstrate the first successful application of the CRISPR/Cas9 system for genome editing in Panagrolaimus sp. PS1159 and the closely related hermaphroditic species Propanagrolaimus sp. JU765 applying the non-homologous end joining and the homology-directed repair (HDR) mechanisms. Using microinjections and modifying published protocols from C. elegans and P. pacificus we induced mutations in the orthologue of unc-22. This resulted in a visible uncoordinated twitching phenotype. We also compared the HDR efficiency following the delivery of different single-stranded oligodeoxynucleotides (ssODNs). Our work will expand the applicability for a wide range of non-model nematodes from across the tree and facilitate functional analysis into the evolution of parthenogenesis, changes in the developmental program of Nematoda, and cryptobiosis.

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