单组分 CRISPR 介导的农杆菌碱基编辑器及其在开发改良菌株系列中的应用

Vincent J. Pennetti, Peter R. LaFayette, Wayne Allen Parrott
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摘要

农杆菌介导的植物转化主要依赖于两个不同的菌株系--C58 和 Ach5。为了更好地服务于植物转化界,我们创建了一套辅助营养和辅助营养重组缺陷突变体,包括 C58 衍生物 EHA105、GV3101::pMP90 和 Ach5 衍生物 LBA4404。虽然这些衍生物很有用,但如果有更多的菌株背景可用,将有助于进一步扩大植物转化的范围。为此,K599(NCPPB 2659)和 Chry5 是两种未充分利用的高病毒性菌株,但它们的解除变体不易获得。为了提高可用性,我们制作了根瘤酵母菌菌株 K599 和肿瘤酵母菌菌株 Chry5 的解除武装版本,并引入了与其他菌系相同的理想突变。通过 CRISPR 介导的适合无义突变的密码子碱基编辑,分别赋予 thyA 和 recA 功能缺失突变,将胸腺嘧啶辅助营养和重组缺陷引入现有的和新解除的农杆菌菌株。为了简化编辑过程,我们创建了一系列可视化标记的单组分碱基编辑器载体和相应的向导过滤 Geneious Prime 封装插件,以加快向导过滤。这些新菌株、简化的 CRISPR 介导的碱基编辑器质粒和简化的工作流程将提高未来农杆菌菌株衍生物的创建难度,同时也为植物转化提供广泛支持。
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Single component CRISPR-mediated base- editors for Agrobacterium and their use to develop an improved suite of strains
Agrobacterium mediated plant transformation largely depends on two distinct strain lineages – C58 and Ach5. To better serve the plant transformation community, we have created a suite of auxotrophic and auxotrophic recombinant deficient mutants of C58 derivatives EHA105, GV3101::pMP90, and Ach5 derivative LBA4404. While these derivatives are useful, having additional strain backgrounds available would help expand the repertoire for plant transformation even further. Toward that end, two underutilized hypervirulent strains are K599 (NCPPB 2659), and Chry5—but disarmed variants are not easily accessible. To improve availability, we produced disarmed versions of A. rhizogenes strain K599 and A. tumefaciens strain Chry5 and introduced the same desirable mutations as with the other lineages. Each thymidine auxotrophy and recombination deficiency were introduced to existing and newly disarmed Agrobacterium strains via loss of function mutations conferred to thyA and recA, respectively, through CRISPR-mediated base-editing of codons amenable to nonsense mutation. To streamline the editing process, we created a series of visually marked single component base-editor vectors and a corresponding guide-filtering Geneious Prime wrapper plugin for expedited guide filtering. These new strains, the simplified CRISPR-mediated base-editor plasmids, and streamlined workflow will improve the ease with which future Agrobacterium strain derivatives are created while also supporting plant transformation at large.
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