Florez-Cardona Valeria, Khani Jessica, McNutt Emily, Manta Bruno, Berkmen Mehmet
New England Biolabs, Ipswich, Massachusetts.
Institut Pasteur de Montevideo, Montevideo, Uruguay.
Curr Protoc. 2025 Jan;5(1):e70088. doi: 10.1002/cpz1.70088.
Functional genomic approaches have been effective at uncovering the function of uncharacterized genes and identifying new functions for known genes. Often these approaches rely on an in vivo screen or selection to associate genes with a phenotype of interest. These selections and screens are dependent upon the expression of proteins encoded in genomic DNA from an expression vector, such as a plasmid. Despite the utility of genomic DNA plasmid libraries, the protocols for their construction have remained unchanged in the past 40 years. Here, we present a procedure for constructing plasmid libraries from genomic DNA. This procedure is scalable and relies on simple techniques and common laboratory equipment and reagents. Briefly, the genomic DNA is extracted and then physically fragmented with a g-TUBE, overhangs are repaired, and fragments are selectively purified with magnetic beads to obtain an average fragment size of 2.5 kb. Blunted fragments are ligated into a blunt-end-digested and dephosphorylated vector. Finally, the library is amplified by electroporating the ligation into a high-transformation-efficiency Escherichia coli strain and extracting the plasmid DNA from the transformants. As a proof of concept, we built and sequenced three genomic libraries from different genomes and calculated their coverage using a next-generation sequencing (NGS) workflow. © 2025 The Author(s). Current Protocols published by Wiley Periodicals LLC. Basic Protocol: Plasmid library construction Alternate Protocol: Selection of gDNA fragments using SageELF gel fractionator Support Protocol 1: Extraction of gDNA with phenol/chloroform Support Protocol 2: Vector preparation.
功能基因组学方法在揭示未表征基因的功能和确定已知基因的新功能方面一直很有效。通常,这些方法依赖于体内筛选或选择,以将基因与感兴趣的表型联系起来。这些选择和筛选取决于从表达载体(如质粒)中基因组DNA编码的蛋白质的表达。尽管基因组DNA质粒文库很有用,但在过去40年中其构建方案一直没有改变。在这里,我们介绍一种从基因组DNA构建质粒文库的方法。该方法具有可扩展性,依赖于简单的技术以及常见的实验室设备和试剂。简而言之,提取基因组DNA,然后用g-TUBE进行物理片段化,修复末端,并用磁珠选择性纯化片段,以获得平均片段大小为2.5 kb的片段。将平端片段连接到经平端消化和去磷酸化的载体中。最后,通过将连接产物电穿孔导入高转化效率的大肠杆菌菌株并从转化体中提取质粒DNA来扩增文库。作为概念验证,我们构建了来自不同基因组的三个基因组文库并进行了测序,并使用下一代测序(NGS)工作流程计算了它们的覆盖率。© 2025作者。由Wiley Periodicals LLC出版的《当前方案》。基本方案:质粒文库构建;替代方案:使用SageELF凝胶分级仪选择基因组DNA片段;支持方案1:用酚/氯仿提取基因组DNA;支持方案2:载体准备。