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Plasmid-Based CRISPR-Cas9 Gene Editing in Multiple Candida Species

机译:多个念珠菌种中基于质粒的CRISPR-Cas9基因编辑

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Many Candida species that cause infection have diploid genomes and do not undergo classical meiosis. The application of clustered regularly interspaced short palindromic repeat-Cas9 (CRISPR-Cas9) gene editing systems has therefore greatly facilitated the generation of gene disruptions and the introduction of specific polymorphisms. However, CRISPR methods are not yet available for all Candida species. We describe here an adaption of a previously developed CRISPR system in Candida parapsilosis that uses an autonomously replicating plasmid. Guide RNAs can be introduced in a single cloning step and are released by cleavage between a tRNA and a ribozyme. The plasmid also contains CAS9 and a selectable nourseothricin SAT1 marker. It can be used for markerless editing in C. parapsilosis , C. orthopsilosis , and C. metapsilosis . We also show that CRISPR can easily be used to introduce molecular barcodes and to reintroduce wild-type sequences into edited strains. Heterozygous mutations can be generated, either by careful selection of the distance between the polymorphism and the Cas9 cut site or by providing two different repair templates at the same time. In addition, we have constructed a different autonomously replicating plasmid for CRISPR-Cas9 editing in Candida tropicalis . We show that editing can easily be carried out in multiple C. tropicalis isolates. Nonhomologous end joining (NHEJ) repair occurs at a high level in C. metapsilosis and C. tropicalis . IMPORTANCE Candida species are a major cause of infection worldwide. The species associated with infection vary with geographical location and with patient population. Infection with Candida tropicalis is particularly common in South America and Asia, and Candida parapsilosis infections are more common in the very young. Molecular methods for manipulating the genomes of these species are still lacking. We describe a simple and efficient CRISPR-based gene editing system that can be applied in the C. parapsilosis species group, including the sister species Candida orthopsilosis and Candida metapsilosis . We have also constructed a separate system for gene editing in C. tropicalis .
机译:许多引起感染的念珠菌具有二倍体基因组,并且不经历经典减数分裂。因此,聚类的规则间隔的短回文重复Cas9(CRISPR-Cas9)基因编辑系统的应用极大地促进了基因破坏的产生和特定多态性的引入。但是,CRISPR方法尚不适用于所有念珠菌。我们在这里描述了使用自主复制质粒的拟南芥假丝酵母中以前开发的CRISPR系统的改编。指导RNA可以在单个克隆步骤中引入,并通过在tRNA和核酶之间的切割而释放。该质粒还含有CAS9和可选择的神经硫菌素SAT1标记。它可用于无毛角衣甲,直角衣甲和角衣甲的无标记编辑。我们还显示,CRISPR可以轻松地用于引入分子条形码,并将野生型序列重新引入已编辑的菌株中。可以通过仔细选择多态性与Cas9切割位点之间的距离或同时提供两个不同的修复模板来生成杂合突变。另外,我们构建了不同的自主复制质粒,用于在热带假丝酵母中进行CRISPR-Cas9编辑。我们表明,可以在多个热带假丝酵母菌中轻松进行编辑。非同源末端连接(NHEJ)修复发生在C. metapsilosis和C.tropicis中。重要念珠菌是全世界感染的主要原因。与感染有关的物种随地理位置和患者人数的不同而变化。热带假丝酵母的感染在南美和亚洲尤为常见,而寄生念珠菌的感染在很小的时候就更常见。仍缺乏操纵这些物种基因组的分子方法。我们描述了一个简单而有效的基于CRISPR的基因编辑系统,该系统可用于C. parapsilosis物种组,包括姊妹念珠菌Orthopsilosis和Candida metapsilosis。我们还构建了一个独立的系统,用于热带念珠菌的基因编辑。

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