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用于铜绿假单胞菌 PAO1 的经序列验证的双等位基因突变体转座子文库。

Sequence-verified two-allele transposon mutant library for Pseudomonas aeruginosa PAO1.

机构信息

Department of Genome Sciences, University of Washington, Seattle, Washington, USA.

出版信息

J Bacteriol. 2012 Dec;194(23):6387-9. doi: 10.1128/JB.01479-12. Epub 2012 Sep 14.

Abstract

Mutant hunts using comprehensive sequence-defined libraries make it possible to identify virtually all of the nonessential functions required for different bacterial processes. However, the success of such screening depends on the accuracy of mutant identification in the mutant library used. To provide a high-quality library for Pseudomonas aeruginosa PAO1, we created a sequence-verified collection of 9,437 transposon mutants that provides genome coverage and includes two mutants for most genes. Mutants were cherry-picked from a larger library, colony-purified, and resequenced both individually using Sanger sequencing and in a pool using Tn-seq. About 8% of the insertion assignments were corrected, and in the final library nearly 93% of the transposon locations were confirmed by at least one of the resequencing procedures. The extensive sequence verification and inclusion of more than one mutant for most genes should help minimize missed or erroneous genotype-phenotype assignments in studies using the new library.

摘要

利用全面的序列定义文库进行突变体筛选,可以鉴定出不同细菌过程所需的几乎所有非必需功能。然而,这种筛选的成功与否取决于所使用的突变体文库中突变体鉴定的准确性。为了为铜绿假单胞菌 PAO1 提供高质量的文库,我们创建了一个经过序列验证的 9437 个转座子突变体的集合,该集合提供了基因组覆盖范围,并包含大多数基因的两个突变体。突变体从一个更大的文库中进行挑选、纯化,并使用 Sanger 测序和 Tn-seq 分别对每个突变体进行测序,然后对突变体进行测序。大约 8%的插入分配被纠正,在最终文库中,几乎 93%的转座子位置通过至少一种重测序方法得到了确认。广泛的序列验证以及为大多数基因包含多个突变体,应该有助于最大限度地减少使用新文库进行研究时基因型-表型分配的遗漏或错误。

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